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FOIA Documents prove COVID-19 "Vaccines" were treated as

"Medical Counter-measures" to a Bio-Weapon attack. Entire
COVID Operation Run by US National Security Council with
NO MANUFACTURING SAFEGUARDS OR DISCLOSURES
NATION HAL TURNER 08 JANUARY 2023  HITS: 206
 
 
New Docs Reveal Department of Defense Controlled COVID-19 Program from the start. The
FDA Vaccine Approval Process was Theater. A combination of the PREP Act, Emergency Use
Authorization, and Other Transactions Authority (OTA), shielded Big Pharma, Agencies,  and
Medical Participants that Delivered Unregulated Vaccines, from any liability.
According to congressionally passed statutes, research of active laws,  and extra details
obtained through the Freedom of Information Act, the Department of Defense owns,
implements, and oversees the COVID-19 vaccine program as a “Countermeasure” to foreign
attack.  While the public was bombarded with an orchestrated fear campaign,  the
U.S. Government managed the Covid response as a national security threat.
The research and documents  were obtained by  a former executive of a pharmaceutical
Contract Research Organization (CRO), Sasha Latypova,  and intensive legal
researcher Katherine Watt.
 
The Three-Legged Stool
The undercover operation was orchestrated utilizing three critical legal maneuvers:
1. Emergency Use Authorization EUA.
2. Prep Act,
3. Other Transactions Authority
 
President Trump declared a Public  Health  Emergency (PHE) on March 13, 2020, under the
Stafford Act, putting the National Security Council in charge of the Covid policy. Covid-19
vaccines are “medical countermeasures” – a grey area of products that are not regulated as
vaccines or medicines.
“They put the National Security Council in charge and treated it as an act of war,” said
Latypova.
According to Operation Warp Speed/ASPR reports, the DoD ordered, oversaw, and tightly
managed the development, manufacture, and distribution of Covid countermeasures, mainly
utilizing the DoD’s previously established network of military contractors and consortia.
Department of Defense (DoD), the  Biomedical Advanced Research and Development
Authority (BARDA), and Department of  Health  and Huma Services (HHS), ordered all Covid
countermeasures, including “vaccines” as prototype demonstrations of large-scale
manufacturing,  avoiding regulations  and transparency under Other Transaction Authority. As
prototypes used under EUA during PHE, Covid countermeasures, including “vaccines,” need
not comply with the U.S. laws for manufacturing quality, safety, and labeling.
“The implication is that the  U.S.  Government authorized and funded the deployment of
noncompliant biological materials on Americans without clarifying their “prototype” legal status,
making the materials not subject to normal regulatory oversight, all while maintaining a
fraudulent pseudo- “regulatory” presentation to the public,” said Latypova.
“Most incredible is the fact that current Laws enacted by the United States Congress appear to
make the coverup actions LEGAL!”
Under the PHE, medical countermeasures are not regulated or safeguarded as
pharmaceutical products (21 USC 360bbb-3(k)).
The American people were led to believe that  the FDA, CDC, and figureheads like Anthony
Fauci, oversaw the COVID-19 vaccine program.  Their involvement was an orchestrated
information operation. All decisions concerning the COVID-19 vaccine research, materials
acquisition, distribution, and information sharing were tightly controlled by the DoD.
Hundreds of Covid countermeasures contracts have been uncovered. Many disclosures are in
redacted form. However, Latypova and Watt have found sources to fill in the details.
A review of these contracts indicates a high degree of control by the U.S. Government
(DoD/BARDA). It specifies the scope of deliverables as “demonstrations” and “prototypes” only
while excluding clinical trials and manufacturing quality control from the scope of work paid for
by the contracts.
To ensure that the Pharma is free to conduct the fake clinical trials without financial risk, the
contracts include the removal of all liability for the manufacturers and any contractors along the
supply and distribution chain under the 2005 PREP Act and related federal legislation.
Why is no action by regulators or courts? According to Latypova and Watt, a combination of
recently passed legislation and executive orders make it LEGAL to LIE! The HHS Secretary is
accountable to no one  if the  Health  National Emergency continues to be extended by
Congress every three months.
A significant information operation was set in motion the minute COVID-19 hit. The U.S.
government, the intelligence community, the media, and Big Tech colluded to orchestrate and
implement an intense pressure campaign designed to get the vaccine legally designated under
the Emergency Use Authorization Act while vilifying dissenting doctors, critics, and viable
alternative treatments. This designation allowed for speedy manufacturing devoid of the
standard safety and public health protocols.
For a vaccine to receive designation under the EUA, there can be no other known treatments
or cures. Therefore, many proven treatments such as ivermectin and hydroxychloroquine were
blacklisted in the media and dismissed as “horse  de-wormers” when these cheap, readily
available drugs were in the past heralded for their effectiveness.
Eminent COVID-treating doctors such as Peter M. McCullough and Pierre Kory have faced
unprecedented attacks on their medical credentials.
 
https://halturnerradioshow.com/index.php/en/news-page/news-nation/foia-documents-prove-
covid-19-vaccines-were-treated-as-medical-counter-measures-to-a-bio-weapon-attack-entire-
covid-operation-run-by-us-national-security-council-with-no-manufacturing-safeguards-or-
disclosures
 
 

The role of the US DoD (and their co-investors) in

"covid countermeasures" enterprise.
Intelligence is never artificial.

Sasha Latypova
Dec 28, 2022
424
325
 
I asked the AI Chat Bot “What was the role of the DoD in covid-countermeasures?” Here
is what it wrote:

“The Department of Defense (DoD) played a significant role in the development

of countermeasures against COVID-19, the disease caused by the novel
coronavirus. The DoD worked closely with other federal agencies, such as the
Department of Health and Human Services (HHS), to respond to the pandemic.
One of the main roles of the DoD in the COVID-19 response was to provide
logistical support and medical resources to help healthcare workers and first
responders on the front lines of the pandemic. The DoD also worked to develop
 and distribute personal protective equipment (PPE) and other supplies to
support the response efforts.
In addition, the DoD provided funding and resources to support the
development of vaccines and treatments for COVID-19.  The Defense
Advanced Research Projects Agency (DARPA), a research arm of the DoD,
played a key role in this effort by funding and supporting the development of
treatments and vaccines through its "Rapid Response Research" program.
Overall, the DoD played a vital role in the response to the COVID-19 pandemic
by providing logistical support, medical resources, and funding for research and
development efforts to combat the disease.”

AI Chat Bot gets a “F” - for a highly controlled narrative answer, which was fed to all MSM
sources, while the “alternative” media did not examine it very much, with some exceptions. It
wasn’t just logistics or even just lots of funding, and certainly nobody was “combatting
disease”.
Thanks for reading Due Diligence and Art! Subscribe for free to receive new posts and support
my work.
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The truth is much more interesting than fiction:
All Covid countermeasures, including the biological warfare agents marketed as
“Covid-19 vaccines”, were ordered by the US DoD as a “large scale manufacturing
demonstration” via Other Transactions Authority contracts.
Hundreds of Covid countermeasures  contracts  became available via FOIA and SEC
disclosures in redacted form.  Review of these contracts indicates a high degree of control by
the US Government (DoD/BARDA) and specifies the scope of deliverables as
“demonstrations” and “prototypes” only.   In other words, the US Government and DOD
specifically ordered a fake theatrical performance from the pharmaceutical manufacturers. Just
to make extra certain that the pharmas are free to conduct the fakery, the contracts include the
removal of all liability for the manufacturers and any contractors along the supply and
distribution chain under the 2005 PREP Act and related federal legislation.
The contracts are structured under Other Transactions Authority (OTA) -  OTA  method of
contracting allows federal agencies to order otherwise-regulated products bypassing any such
regulations, as well as financial accountability mechanisms that cover standard government
contracting, and other laws that regulate disclosure and Intellectual Property (IP) derived from
publicly funded research.
“Other” is a catchall category that is not a contract, not a research grant, not a procurement,
etc.: not any normally regulated/accountable government contracting. 
Here is a typical contract scope for “vaccines”:

 
While the DOD/BARDA countermeasure contracts refer to safety and efficacy requirements for
vaccines and mention current Good Manufacturing Practices (cGMP) compliance, these items
are explicitly carved out as not being paid for nor ordered by the US Government. 

 
This gets even more interesting when we examine some of the redactions in contracts:
 
I know what is in the redacted part of the above paragraph and it was not hard to figure out.
The first redaction under 1.1.1 BACKGROUND is “Fosun Pharmaceuticals”, so the sentence
reads “Fosun Pharmaceuticals”, Pfizer and BioNTech entered into an agreement for the co-
development…”
Note: the only journalist I am aware of in either “mainstream” or “resistance” who mentioned
Fosun was Naomi Wolf, kudos to her. I was in touch with The Epoch Times to try to publish
this information, and even they decided to bury the story (but they published my other
materials). I did discuss this on Dr. Jane Ruby’s show, and kudos to her as well for not being
afraid to cover the truth.
 
Pfizer-BioNTech is really a 3-party R&D alliance: Fosun-Pfizer-BioNTech, and by “party” I
mean that one of the three is the Chinese Communist Party. Fosun is a huge
Chinese conglomerate that owns a large number of global companies, and its chairman Guo
Guangchang is a very high ranking member of the CCP. It is curious that the US DoD awarded
$10 billion (Pfizer’s Operation Warp Speed/DoD/BARDA contract) to a venture whose
substantial equity (and IP) holder is the the Chinese Communist Party. For avoidance of doubt:
 
Below is the timeline of some of the key investments and R&D deals I was able to identify from
public SEC shareholder disclosures, immediately preceding and following the “pandemic”:
 
 
Just to make sure, we are talking about the exact technology in the mRNA shots. Here is the
definition from March 17, 2020 agreement between Pfizer and BioNTech (p. 4):

 
The same document describes a data sharing agreement, “pharmacovigilance” globally
among the 3 parties. They will count the bodies and share the data with each other:
 
On the “pharmacovigilance” aspect, there is a 4th participant in this arrangement - the Israeli
Ministry of Health, which entered into a data sharing agreement with Pfizer on January 6, 2021
and gave Pfizer (and by extension, US DoD and anyone who controls it, BioNTech and anyone
who controls it, Fosun and anyone who controls it, i.e. CCP) access to all their citizens’
centralized electronic health records. But don’t worry, Benjamin Netanyahu promised to keep
the data de-identified. Right.
 
Side note - Israeli government recently “misplaced” the Manufacturing and Supply Agreement
with Pfizer mentioned in the data sharing agreement above (so we know for sure it exists). The
government sadly cannot find it for some reason…

bad cattitude
israeli government "lost the agreement" with pfizer for covid vaccines
so, apparently, the great risk of working from home is the VAST seeming increase in “the dog
eating your homework.” but this is really something. israel, who everyone around the world
was looking to fo…
Read more
19 days ago · 657 likes · 278 comments · el gato malo
This gets even larger and more interesting when looking at the sources of “R&D” financing.
Turns out, there were numerous financial backers and co-investors in the BioNTech “venture”
in the years preceding the global fraud and mass murder exercise. According to Crunchbase,
BioNTech, a tiny company with just a handful of employees and NO PRODUCTS or scale
manufacturing, raised $1.7B in 9 rounds of investments since around 2008. Large portion of
the money, $1B+ was raised before 2020. What was it for, since no big clinical trials or scale
manufacturing was happening then? That’s a good question, worth examining at some point.
Cursory review of some of the investment rounds indicates wide and very international
involvement of a variety investors from US, Europe, UK, Australia, South Africa, mainland
China, Hong Kong and Singapore among others. These likely included many government
actors: “sovereign” funds, pension funds and the like who often do these investments by
allocating money to “private venture funds” (limited partners in a private venture funds are
confidential). Maybe I will do a separate article on this at a later date.
Note, many people ask me “what about China and Russia?” when I talk about our own
government and DoD engaged in mass genocide of Americans. I answered about China - they
are allied with the US DoD on this. The CCP is profiting from the financial windfall of the US
government printing dollars and throwing them into the mRNA furnaces where they are driving
masses of the brainwashed citizens to suicide themselves. China claims to use “traditional
vaccines” - if you believe what the Chinese say, I have a bridge to sell you.
I have not seen evidence of any similar alliance with Russia. This makes sense, because
ultimately this boils down to the war of US vs Russia using proxies and alliances (as it always
does). This does not mean that Russia are “the good guys”. Simply that the owners of Russia
(whoever they are, not necessarily based in Russia) disagree with the owners of the US
(whoever they are, not necessarily based in the US). Russia is running the same “covid script”,
using knock off RNA/DNA injections, probably buying materials from the same suppliers, and
also using war to kill off their own younger population. It’s just that they are doing it for THEIR
OWN interests, not that of the US and their allies.
Back to this western continent - we have already established that “Covid-19 vaccines” are
biowarfare agents, legally not medicines, not pharmaceuticals, and not regulated as such.
Use of Emergency Use Authorized (EUA) covered countermeasures under a declared
Public  Health  Emergency cannot constitute a clinical investigation (21 USC 360bbb-
3(k)), therefore these countermeasures could not be tested for safety or efficacy in
accordance with US law (21 CFR 312 and 21 CFR 601), nor could compliance with
current Good Manufacturing Practices (cGMP) or Good Distribution Practices (GxP in
general) be enforced by the FDA. 
This legal fact was known to the US Government, DOD, BARDA, FDA, CDC, HHS officials
signing the contracts, involved in the OWS, and it was also known to Pfizer, Moderna and
other pharma companies. mRNA technology has always been designated dual-use, a
category of bioweapons:
Due Diligence and Art
mRNA Injections as a Dual-Use Technology – Assessment of Threat of Misuse as Biological
and Chemical Weapons.
In politics, diplomacy, and export control, "dual-use" refers to technology that can be used for
both peaceful and military aims. mRNA technology, including embodiments as injectable drugs
or vaccine products, has been long identified as a dual-use technology. See references…
Read more
a month ago · 59 likes · 31 comments · Sasha Latypova
From the start, “covid pandemic” was treated by the US Government as a national security
matter  (i.e. war)  and covid policy was set by the National Security Council (assemblage of
Defense and Intelligence heads), not HHS.
March 13, 2020:  “PanCAP Adapted  U.S. Government COVID-19 Response
Plan” (PanCAP-A) states that United States policy in response to SARS-CoV-2 is set not by
the public health agencies designated in pandemic preparedness protocols (Pandemic and All
Hazards Preparedness Act,  PPD-44, BIA), but rather by the National Security Council, or
NSC.  NSC does not have regular attendees from public  health  agencies and its focus is
national security and foreign policy matters." 
Below is the organization chart from the PanCAP-A document, p.9:

 
When a known weaponizable tech is given a liability-free, extrajudicial status shielded from
all regulations, it’s not hard to put 2 and 2 together. The national security, DoD and Intelligence
officials absolutely knew all of this. They went ahead and authorized a $10 billion
purchase order of this weaponizable tech from the Fosun-Pfizer-BioNTech enterprise (backed
by numerous foreign governments including the Chinese), to deliver and deploy it onto
Americans, during the time of war.
I think by now it should become clear that the “5th gen warfare” is not just the use of psyops
and total control of social media by the FBI and CIA (that’s so last century!) It’s also not “profits
over safety”, “bad FDA overlooked myocarditis” or “big pharma pays politicians for election
campaigns”. We are way, way past that. I keep pointing out that if the motive were JUST
PROFIT, then the most profitable strategy would have been to ship placebo. They would not
be violating any laws by doing so, there would be no adverse events and deaths, the product
would look perfectly cGMP compliant, while covid would have gone away quickly by itself. Yet,
the governments (plural)-pharma cartel insists on killing and injuring millions of people,
obviously limiting the profit potential by doing so.
The current war is the war of the global governments (plural), that only pretend to be at odds
with each other, marketing themselves as “left”, “right”, “communists”, “green”, “capitalists”,
“socialists”, “populists”, “conservatives”, etc. etc. in a never ending clown show of the political
theater. Behind the scenes, the “official enemies” are partners and co-investors into “joint
ventures” against us, people of the world. They use taxpayers’ money to fund, develop, then
“approve”, purchase and deploy prohibited biowarfare agents for killing and injuring their own
civilian population, their own armed forces, first responders, healthcare workers,
pregnant women and children. To stop this every one of us must start using correct precise
language, start calling things what they really are.
 
https://sashalatypova.substack.com/p/the-role-of-the-us-dod-and-their?
publication_id=870364&post_id=91532704&isFreemail=true
 
 

American Domestic Bioterrorism Program

Building the case to prosecute members of Congress, presidents, HHS and
DOD secretaries and federal judges for treason under 18 USC 2381.

Katherine Watt
 
Apr 28, 2022
434
283
 
Research and organizing tool first posted April 28, 2022, subject to ongoing revision as new
information comes to light. Last updated Dec. 22, 2022.
Other formats:  Sept. 2022 small-print PDF  (67 pages);  Sept. 2022 large-print PDF  (101
pages); Nov. 2022 Statutory History Orientation Memo (45 pages); Dec. 2022 Legal Structures
Outline (2 pages), Dec. 2022 Six Statutory Frameworks - Executive Summary (14 pages)

OVERVIEW

 
I started looking closely at the legal architecture supporting the Covid national
prison panopticon on Jan. 30, 2022, after hearing Attorney Todd Callender’s interview, which
provided information about the American domestic legal framework; how it fit with the oddly-
coordinated pandemic story told by governments worldwide; and how it relates to the
World Health Organization International Health Regulations of 2005 at the center.
I wrote up the interview:

Legal Walls - Short Version

Legal Walls of the Covid-19 Kill Box; PDF

Prior to that day, I’d spent a lot of time, with increasing confusion and alarm and despair, trying
to figure out why the U.S. Constitutional legal system hadn’t put a stop to the nonsense as its
nonsensicality became obvious to so many people.
Why did it continue, with no end in sight, and not even a glimpse of a path to the end?
Since then, as I’ve dug into Callender’s analysis following the supporting paper trails, I’ve
learned why, and how.
A whole lot of things that once were federal and state crimes and civil rights violations have
been legalized by Congress through legislative, statutory revisions to the United States Code,
signed by US Presidents, and implemented at the administrative, regulatory level by the
Department of Health and Human Services and Department of Defense through the Code of
Federal Regulations.
I’ve reported on those findings in small bits and pieces, connecting the laws to court cases,
executive orders, guidance documents for industry and researchers, academic papers,
intellectual property patents, regulatory amendments, psychological manipulation programs,
geopolitical developments and other facts as they’ve floated across my field of view.
I think the critical decay began around 1983, when the ‘public health emergencies’ section was
added to the 1944 Public Health Service Act, although the 1944 PHSA itself represented an
additional militarization of human medicine in the United States.
Most of the worst laws have been passed since 2000 — just before 9/11 and the US
Department of Defense false flag anthrax attacks.
They are listed below, with links to the full text of each law, and a short summary of what I
understand about how each one fits into the overall scheme.
The basic goal of the architects, which has been achieved, was to set up legal conditions in
which all governing power in the United States could be automatically transferred from the
citizens and the three Constitutional branches into the two hands of the  Health  and Human
Services Secretary, effective at the moment the HHS Secretary himself declared a
public health emergency, legally transforming free citizens into enslaved subjects.
That happened on Jan. 31, 2020, in effect as of Jan. 27, 2020 through the present day.
In other words: Congress and US Presidents legalized and funded the overthrow of the
U.S. Constitution, the U.S. government and the American people, through a massive
domestic bioterrorism program relabeled as a public health program, conducted by the
HHS Secretary and Secretary of Defense on behalf of the World Health Organization and
its financial backers.

Navigation Tool/Jump To:

1900-1929
1930-1939
1940-1949
1950-1959
1960-1969
1970-1979
1980-1989
1990-1999
2000-2009
2010-2019
2020-2022

Related reporting:

COVID-19 injectable bioweapons as case study in legalized, government-operated

domestic bioterrorism
Faked Clinical Trials and 'Real World Evidence'
US federal crimes for which there is evidence to prosecute Covid-19 bioterrorists who
occupy US government positions
22 worst Congressional bioterrorism authorization and funding laws passed since 1983
Run-up to the American bioterrorist State’s Jan. 31, 2020 declaration of war - Part
1 (2014-2017)
 Run-up to the American bioterrorist State’s Jan. 31, 2020 declaration of war - Part
2 (2018-2020)
Timeline (1819-2022) of Supreme Court cases, related state cases and treatises

1900-1929 - Presidents Theodore Roosevelt, William Howard Taft, Woodrow Wilson,

Warren Harding, Calvin Coolidge, Herbert Hoover

 
 

1907 - Treaty at the Hague — Convention Respecting the Laws and Customs of War on
Land, including Section III, Military Authority Over the Territory of the Hostile State: “Art.
42. Territory is considered occupied when it is actually placed under the authority of the
hostile army.”
1909 - Launch of the  Round Table Movement. “By 1919, the Round Table Movement
changed its name to the  Royal Institute for International Affairs  (aka: Chatham  House)
with the Round Table name relegated to its geopolitical periodical… in America, where
knowledge of the British Empire’s subversive role was more widely known, the name
“American Institute for International Affairs” was still too delicate. Instead the name
Council on Foreign Relations” was chosen and was chartered in 1921.”
1913/12/23 - US Congress and President Wilson passed Federal Reserve Act. PL 63-
43,  38 Stat. 251. Created Federal Reserve Bank, central banking system in United
States.
1921/11/23 - US Congress and President Harding passed Sheppard-Towner Maternity
and Infancy Protection Act. PL 67-97, 42 Stat. 224. Established status of American-born
babies — human beings — as collateral for national debt owed to international bankers;
program operated through birth certificates/security bonds filed with state registries of
vital statistics. Expired 1929, replaced by 1935 Social Security Act.

1930-1939 - Presidents Herbert Hoover, Franklin D. Roosevelt

 
 

1933/04/05 - President Roosevelt signed  Executive Order 6102, under state of

emergency (Great Depression). Ratified by Congress through  House  Joint Resolution
192. Forbade the hoarding 'of gold or silver coin or bullion or currency,' confiscated gold
held by private individuals, to remove the constraint on the Federal Reserve (1913
Federal Reserve Act) preventing it from increasing the money supply.
 1933/06/05 - Congress passed  House Joint Resolution 192, ratifying President
Roosevelt’s Executive Order  6102; declared bankruptcy of US government; suspended
gold standard; pledged lives of American people (registered at birth through Social
Security program) as collateral/debt slaves to international bankers, against national
debt.
1933/06/12 - London Economic Conference began. Report on Matthew Ehret,  Clash of
the Two Americas: Open vs. Closed Systems Collide:  How Roosevelt Halted Previous
Attempts to Implement a New World Order.
1935/08/14 - US Congress and President Roosevelt passed Social Security Act - PL 74-
271. 49 Stat. 620. Social Security Act governs Medicare and Medicaid, two of the federal
authorization and funding pathways through which ‘breakthrough’ devices and drugs,
fast-track products, products eligible for accelerated approval and other FDA-classified
products are developed, manufactured and used on humans. Amendments to SSA since
1983 and pending, have expanded/will further expand the novel drug and
device/bioweapon classes eligible for fast-tracked federal research and deployment
funding within the Medicare/Medicaid programs.
1938/06/25 - Congress and President Roosevelt passed  Federal Food Drug and
Cosmetic Act  (FDCA). PL 75-717,  52 Stat. 1040. Original stated purpose: “to prohibit
the movement in interstate commerce of adulterated and misbranded food, drugs,
devices, and cosmetics.” Codified at 21 USC 9. By the outbreak of Covid in late 2019,
FDCA had been amended by several decades of Congressional acts to become one of
the key laws under which the American domestic bioterrorism program is authorized,
funded and operated.
1939/09/01 - Globalists launched World War II.

1940-1949 - Presidents Franklin D. Roosevelt, Harry S. Truman

 
 

1944/07/01 - 07/22 - Globalists negotiated  Bretton Woods Articles of Agreement  to

establish a centralized global financial and banking system.
1944/07/01 - Congress and President Roosevelt passed  Public  Health  Service
Act  (PHSA). PL 78-410,  58 Stat. 682. Consolidated, centralized and militarized the
American public  health  system that had developed within several agencies since the
Revolution. Codified at 42 USC 201.
1945/04/12 - President Roosevelt died; President Truman took office.
1945/07/31 - Congress and President Truman passed Bretton Woods Agreement Act, PL
79-171,  59 Stat. 512, authorizing President to accept membership in International
 Monetary Fund and International Bank for Reconstruction and Development, later known
as World Bank.
1945/09/02 - Globalists ended World War II.
1945/10/24 - Globalists established United Nations. US Congress ratified treaty.
1945/11/20 - Globalists began Nuremberg trials.
1945/12/27 - Bretton Woods Agreement entered into force.
1945/12/29 - Congress and President Truman passed International Organizations
Immunities Act, PL 79-291, 59 Stat. 669. Corey Lynn report - Laundering with Immunity:
The Control Framework, Sept. 29, 2022.
1946/06/11 - Congress and President Truman passed Administrative Procedures Act, PL
79-404. 60 Stat. 237. Established framework for the administrative state to operate within
a  de facto  executive branch dictatorship, through the “committed to agency discretion”
override of both the legislative process and judicial review. Codified at 5 USC 551.
1946/07/22 - Globalists established the World Health Organization and adopted the WHO
Constitution, signed by 61 nations at International  Health  Conference in  New York, to
enter into force as of 04/07/1948. WHO Constitution amendments passed by
World Health Assembly 02/03/1977 ; 01/20/1980 ; 07/11/1994 ; 09/15/2005.
1946/10/01 - Globalists concluded Nuremberg trials.
1947 National Security Act - 61 Stat. 499. Set up precursors to Federal Emergency
Management Agency (FEMA).
1947/10/30 - Globalists adopted General Agreement on Tariffs and Trade (GATT) treaty.
1948 - UN Universal Declaration of Human Rights, part of International  Bill  on Human
Rights
1948 US Information and Educational Exchange Act (Smith-Mundt). PL 80-402. 62 Stat.
6. Set up programs for US propaganda distribution in foreign countries; limited use of
government propaganda on American population. ‘Modernized’ to authorize domestic
propaganda in 01/02/2013 National Defense Authorization Act.
1948/01/01 - General Agreement on Tariffs and Trade (GATT) treaty entered into force.
1948/04/07 - World Health Organization Constitution entered into force.
1948/06/14 - Congress authorized President Truman to accept membership in
World Health Organization on behalf of US government. PL 643, 64 Stat. 441. Codified
at 22 USC 290.
1949/04/04 - US Senate ratified North Atlantic Treaty Organization (NATO) treaty.
1949/06/18 - George Orwell published 1984.
1949/08/24 - NATO treaty entered into force.
1949 - Geneva Conventions

1950-1959 - Presidents Harry Truman, Dwight Eisenhower

 
 

1951/05/25 - Globalists adopted first International Sanitary Regulations at

the  World  Health  Organization World  Health  Assembly, to enter into force 10/01/1952.
International Sanitary Regulations were revised and renamed
International  Health  Regulations in 1969. Revised again 1973, 1981, 2005. Draft
revisions under review 2022.
1951 - Globalists adopted UN Convention on the Prevention and Punishment of the
Crime of Genocide.
1952/09/14 - Roman Catholic  Pope Pius XII presented speech  On the Moral Limits of
Medical Research and Treatment to First International Congress on Histopathology of the
Nervous System. “Insofar as the moral justification of the experiments rests on the
mandate of public authority, and therefore on the subordination of the individual to the
community, of the individual’s welfare to the common welfare, it is based on an erroneous
explanation of this principle. It must be noted that, in his personal being, man is not finally
ordered to usefulness to society. On the contrary, the community exists for man.”
1952/09/27 - President Truman signed Executive  Order  10399 establishing the US
Surgeon General as the “health  administrator” for the World  Health  Organization on
American soil, under 1948 WHO Constitution and 1951 WHO International Sanitary
Regulations. 17 Federal Register 8648.
1952/10/01 - WHO International Sanitary Regulations of 1951 entered into force in WHO
member states.
1953/03/12 - President Eisenhower transmitted Reorganization Plan No. 1 of 1953 to
Congress, subordinating US sovereignty to WHO International Sanitary Regulations, to
be implemented by Surgeon General through the Department of Health, Education and
Welfare (later renamed Health and Human Services). 18 Federal Register 2053. Codified
at 42 USC 202.

1960-1969 - Presidents Dwight Eisenhower, John F. Kennedy, Lyndon Johnson, Richard

Nixon

 
 

1961/01/17 - President Eisenhower delivered  Farewell Address, warning Americans of

the military-industrial-Congressional complex and the “danger that public policy could
itself become the captive of a scientific-technological elite.”
 1962/10/11 - Roman Catholic Pope John XIII convoked Second Vatican Council (Vatican
II). Through the council, Satanic globalists expanded and deepened their infiltration
to destroy the institutional Catholic Church and weaken Catholic faith around the world.
1963/06/30 - Enthronement of Lucifer ceremony  coordinated with consecration of Pope
Paul VI.
1963/11/22 - President Kennedy assassinated; President Johnson took office.
1964/06 - Globalists adopted the  Declaration of Helsinki  on ethics of human
experimentation, through World Medical Association.  Revised seven times since: 1975,
1983, 1989, 1996, 2000, 2008, 2013.
1965/12/08 - Roman Catholic Pope Paul VI concluded Second Vatican Council.
1966/04/25 - President Johnson transmitted Reorganization Plan No. 3 of 1966 to US
Congress, transferring US Surgeon General’s authorities to Secretary of  Health,
Education and Welfare department, effective 06/25/1966. 31 Federal Register 8855.
1968/04/04 - Assassination of Martin Luther King Jr.
1968/06/06 - Assassination of Robert F. Kennedy.
1968/07/25 - Roman Catholic Pope Paul VI issued papal encyclical  Humanae Vitae  on
meaning of human life, and Catholic prohibition of abortion and contraception.
1969 -  Globalist  - WHO International Sanitary Regulations, in effect since 10/01/1952,
revised and renamed International Health Regulations. Revised again 1973, 1981, 2005.
Draft revisions under review 2022.
1969/06/09 - Dr. Donald MacArthur testified to  US Senate hearing on DOD
appropriations, about development of “new infective microorganisms which could differ in
certain important aspects from any known disease-causing organisms. Most important of
these is that it might be refractory to the immunological and therapeutic processes upon
which we depend to maintain our relative freedom from infectious disease.”
1969/11/19 - Congress and President Nixon passed Armed Forces Appropriations Act.
PL 91-121, 83 Stat. 209. Section 409 authorized Department of Defense to use human
subjects for experiments in chemical and biological weapons, established reporting
requirements (DOD reports to Congress) codified at 50 USC 1511(a) and authorized
President to suspend informed consent and other provisions during a declared war or
national emergency, codified at 50 USC 1515. Congressional reporting requirements
amended 1977 and 1982, repealed 1996.
1969/11/25 - President Nixon  Statement on Chemical and Biological Defense Policies
and Programs
1969/11/30 - New  Ordo Missae, “liturgical innovation,” introduced by Pope Paul VI,
breaking the tradition of centuries.

1970-1979 - Presidents Richard Nixon, Gerald Ford, Jimmy Carter

 
 

1970 - Globalists, through Club of Rome, published The Predicament of Mankind: Quest

for Structured Responses to Growing World-wide Complexities and Uncertainties, A
Proposal
1970 - Zbigniew Brzezinski published Between  Two Ages: America’s Role in the
Technotronic Era.
1970/03/16 - Congress and President Nixon passed An Act to Establish a Commission
on Population Growth and the American Future. PL 91-213, 84 Stat. 67.
1970/08/15 - Congress and President Nixon passed Economic Stabilization Act of 1970.
PL 91-379, 84 Stat. 799. Authorized President to stabilize prices, rents, wages, salaries,
interest rates, dividends and similar transfers as part of a general program of price
controls within the American domestic goods and labor markets. Used by Nixon in
August 1971.
1970/10/26 - Congress and President Nixon passed Legislative Reorganization Act. PL
91-510, 84 Stat. 1140.
1970/11/01 - Roman Catholic Archbishop Marcel Lefebvre founded  Society of St. Pius
X to preserve traditional Catholic teachings in the wake of the Second Vatican Council.
1971 - Globalists, through Henry Kissinger and Klaus Schwab, established the World
Economic Forum.
1971 - President Nixon launched the War on Drugs
1971/01 - Six banks in the European Community, under Jacob Rothschild’s direction,
consolidated into Inter-alpha Group of Banks.
1971/08/15 - President Richard Nixon directed the Treasury Secretary to suspend, with
some exceptions, the convertibility of the dollar into gold or other reserve assets, ordering
the gold window to be closed such that foreign governments could no longer exchange
their dollars for gold, and issued Executive  Order  11615 (pursuant to the  Economic
Stabilization Act of 1970), imposing a 90-day freeze on wages and prices in  order  to
counter inflation.
1971/08 - US Department of Health, Education and Welfare, National Institutes of Health,
National Cancer Institute published Special Virus Program, Progress Report 8
1971/12/23 - US Congress and President Nixon passed National Cancer Act. PL 92-
216,  85 Stat. 778. Expanded US government bioweapons development and programs
under pretext of cancer research.
1972 - Globalists, through Club of Rome, published Limits to Growth, expanding on 1970
proposals in Predicament of Mankind.
1972 - Globalists, through Bulletin of the World Health Organization, published two-part
series on Virus-associated immunopathology: animal models and implications for human
disease,  Part 1  and  Part 2, addressing potential of lab-developed viral, communicable
bioweapons to cause cancers and other life-limiting autoimmune and immune
dysregulation disorders.
1972/04/10 - Globalists opened UN Convention on the Prohibition of the Development,
Production and Stockpiling of Bacteriological (Biological) and Toxin Weapons and on
their Destruction  for signing, leaving major loopholes for biological and toxic agents
allegedly developed for ‘protective’ or ‘prophylactic’ purposes.
1972/08 - US Department of Health, Education and Welfare, National Institutes of Health,
National Cancer Institute published Special Virus Program, Progress Report 9
1973 - Trilateral Commission
1973/01/22 - US Supreme Court issued ruling in Roe v. Wade, 410 US 113, on abortion,
eroding moral status of human beings based on developmental status/age and finding a
‘right’ to abortion in the US Constitution.
1974/04/01 - Richard Gardner published essay in Foreign Affairs:  The Hard Road to
World Order. “In short, the ‘house of world order’ will have to be built from the bottom up
rather than from the top down. It will look like a great ‘blooming, buzzing confusion,’ to
use William James’ famous description of reality, but an end run around national
sovereignty, eroding it piece by piece, will accomplish much more than the old-fashioned
frontal assault.”
1974/04/24 - Secretary of State Henry Kissinger promulgated National Security Study
Memorandum 200,  Implications of Worldwide Population Growth for U.S. Security and
Overseas Interests. NSSM 200 directed Secretary of Defense, Secretary of Agriculture,
CIA Director, Deputy Secretary of State and Administrator for US Agency for International
Development to study international political and economic implications of population
growth and offer possible courses of action for the U.S. The resulting Kissinger Report
was sent to President Nixon 12/10/1974.
1974 Disaster Relief Act. PL 93-288. Another statute creating precursors to FEMA.
1974/07/12 - US Congress and President Nixon passed National Research Service
Award Act. PL 93-348, 88 Stat. 342. Title II set up a commission to study bioethics and
protection of human subjects. Led to 1977  Health, Education and Welfare report and
1979 Belmont Report.
1974/08/09 - President Nixon resigned; Gerald Ford took office.
1974/11/21 - Roman Catholic Archbishop Marcel Lefebvre, founder of Society of Saint
Pius X, published 1974 Declaration on modernism and preservation of the Catholic faith
against destructive assaults subsequent to Second Vatican Council.
1974/12/10 - Secretary of State Henry Kissinger’s National Security Study Memorandum
200 (NSSM 200) study completed as the  Kissinger Report, establishing global
depopulation as US geopolitical strategy.
1974/12/31 - US Congress and President Ford legalized private ownership of gold,
reversing 1933 prohibition. PL 93-373.
1975/03/26 -  UN Convention on the Prohibition of the Development, Production and
Stockpiling of Bacteriological (Biological) and Toxin Weapons and on their
Destruction entered into force. Codified in US law at 18 USC 175 in 1990. Both the UN
convention and the US law left major loopholes for biological and chemical agents
developed for ‘protective’ or ‘prophylactic’ purposes. World  Health  Organization, United
Nations, World Economic Forum and US government drove the global bioterrorism
program through those loopholes, through swine flu/H1N1, AIDS, anthrax, smallpox,
MERS, SARS, SARS-CoV-2 and other communicable and injected pathogens.
1975/06 - Rockefeller Commission published  Report to the President on CIA Activities
Within the US.
1975/11/26 - President Gerald Ford endorsed the Kissinger Report’s depopulation plan
through National Security Decision Memorandum 314
1976/01 - Swine influenza/H1N1 outbreak started at Fort Dix; in April, Congress funded a
vaccine development/mass vaccination through Merck; in late September injections
began. Heart attacks, Guillain-Barre syndrome, deaths and other adverse effects
resulted. In December, campaign suspended and never restarted.
1976/03/23 - UN International Covenant on Civil and Political Rights entered into force.
1976/04 - Senator Frank  Church  Commission published a  Report on the Foreign and
Military Intelligence Activities of the United States  in April 1976. The  Church  report
included, at Chapter 15-F, information about chemical and biological activities, and at
Chapter 17, information about “Testing and Use of Chemical and Biological Agents by the
Intelligence Community.” It reported on Project Chatter, Project Bluebird/Artichoke, MK-
ULTRA, MK-NAOMI and other programs through which the US Government conducted
experiments on human subjects against their will and to their detriment.
1976/09/14 - Congress and President Ford passed National Emergencies Act - PL 94-
412, 90 Stat. 1255. Codified at 50 USC 34. This is one of the key laws cited in George W.
Bush’s Sept. 14, 2001 Proclamation 7463, Declaration of National Emergency by Reason
of Certain Terrorist Attacks  and renewed every year since, most recently by Biden in
Sept. 2021. It’s also one of the laws cited in Donald Trump’s March 13, 2020
Proclamation 9994, Declaring a National Emergency Concerning the Novel Coronavirus
Disease (COVID–19) Outbreak,  renewed every year since, most recently by Biden in
Feb. 2022.
1977/01/14 - US Department of  Health, Education and Welfare published report on
informed consent of human subjects of biomedical experiments, 45 CFR 46, Protection of
Human Subjects: Research Involving Prisoners and Notice of Report and
Recommendations of the National Commission for the Protection of Human Subjects of
 Biomedical and Behavioral Research, in compliance with 1974 National Research
Service Award Act. 42 Federal Register 3076.
1977/07/30 - Congress and President Carter passed Department of Defense
Appropriations Authorization Act of 1978. PL 95-79, 91 Stat. 323. Section 808 addressed
DOD use of military personnel as research subjects for biological and chemical weapons
under 1969 law, codified at 50 USC 1520; required notice to be given to local officials
before subjecting civilian populations to chemical and biological weapons tests; required
DOD reporting to Congress. The provision on DOD reporting to Congress was amended
in 1982 and repealed in 1996. Other provisions of the law were amended in 1997 to
expand experimentation on military personnel, through the NDAA for FY1998 at Section
1078 and the Emergency Use Authorization provisions of the 1997 Food and Drug
Administration Modernization Act at Section 402.
1979/04/18 - National Commission for the Protection of Human Subjects of

Biomedical and Behavioral Research published the Belmont Report on ethics of human

subjects research, in compliance with 1974 National Research Service Award Act and
informed by 1977 HEW report and recommendations.
1979/10/17 - Congress and President Carter passed Department of Education
Organization Act. PL 96-88,  93 Stat. 668. Section 509 redesignated the US  Health,
Education and Welfare Department as the  Health  and Human Services Department.
From that point to the present, the Secretary of  Health  and Human Services has
exercised authorities under the WHO Constitution and WHO
International Health Regulations, as transferred from Surgeon General to HEW Secretary
in 1966.

1980-1989 - Presidents Ronald Reagan, George H.W. Bush

 
 

1980 Comprehensive Environmental Response, Compensation and Liability Act. PL 96-

510, 94 Stat. 2767. Superfund Act. Set up federal programs for cleanup of toxic chemical
dumpsites.
1980/06/16 - US Supreme Court ruling in Diamond v. Chakrabharty, 447 US 303. Held: A
live, human-made micro-organism is patentable subject matter under 35 USC 101.
1981/06/01 - HHS-Food and Drug Administration Final Rule  Protections for Human
Subjects; Prisoners Used as Subjects in Research, 21 CFR 50, implementing 1979
recommendations of National Commission for the Protection of Human Subjects of
Biomedical and Behavioral Research, went into effect. 45 Federal Register 36386
1981/07/27 - HHS-FDA Final Rule Protection of Human Subjects;
Informed Consent  (21 CFR 50.20) and  Protection of Human Subjects; Standards for
Institutional Review Boards for Clinical Investigations  (21 CFR 56.101) went into
effect. 46 Federal Register 8942. Both were amended many times thereafter.
1982 - Roussel-Uclaf developed RU-486/mifepristone chemical abortion pill. Approved by
US FDA in Sept. 2000.
1982/12/21 - Congress and President Reagan passed Congressional Reports
Elimination Act. PL 97-375,  96 Stat. 1822. Section 203(a) amended requirements for
DOD report to Congress on use of human subjects in chemical and biological weapons
research under 50 USC 1511(a). Reporting requirement repealed by Congress,
02/10/1996, PL 104-106 at Section 1061(k).
1983/07/13 - Congress and President Reagan passed Public  Health  Service Act
Amendment. PL 98-49, 97 Stat. 245. Section 319 amended Public Health Service Act to
add a ‘Public Health Emergencies’ program, granting new powers to Health and Human
Services Secretary and establishing a $30 million slush fund called the
Public Health Emergencies Fund. Codified at 42 USC 247d. Summary posted April 20,
2022.
1983/12/22 - President Reagan signed Executive  Order  12452, listing communicable
diseases subjecting citizens to forcible apprehension and detention under  Health  and
Human Services Secretary’s quarantine authority through PHSA, 42 USC 264b, including
"Cholera or suspected Cholera, Diphtheria, infectious Tuberculosis, Plague, suspected
Smallpox, Yellow  Fever, and suspected Viral Hemorrhagic Fevers (Lassa, Marburg,
Ebola, Congo-Crimean, and others not yet isolated or named).”  48 Federal Register
56927
1985/11/20 - Congress and President Reagan passed  Health  Research Extension Act.
PL 99-158,  99 Stat. 877. Section 498 prohibited HHS from funding or conducting fetal
tissue research for three years. Codified at 42 USC 299g.
1986/03/29 - Robert Strecker delivered to Congress and published report on AIDS
outbreak:  This Is a Bioattack Alert. Report connected US government cancer virus
research to virus-induced immune system disorders and cancer in AIDS patients.
1986/07/13 - Congress and President Reagan passed Superfund Amendments and
Reauthorization Act. PL 99-499,  100 Stat. 1613. Title III, Emergency Planning and
Community Right to Know Act related to toxic chemicals and federal government
authority.
1986/08/27 - Roman Catholic Archbishop Marcel Lefebvre published  Letter to 8
Cardinals Regarding the Assisi Affair, addressing dangers to the Catholic faith presented
by Pope John Paul II’s planned Interfaith Peace Service.
1986/09/18 - Roman Catholic Pope John Paul II conducted multi-religious Interfaith
Peace Service in Assisi, Italy.
 1986/11/14 - Congress and President Reagan passed State Comprehensive
Mental Health Services Plan Act - PL 99-660, 100 Stat 3743. Title III, National Childhood
Vaccine Injury Act, amended Public Health Service Act to establish and fund a National
Vaccine Program; grant vaccine manufactures legal immunity for injuries and deaths
caused by their products; establish and fund a tax revenue/debt-funded National Vaccine
Injury Compensation Program. Codified at 42 USC 300aa.
1986/12/02 - Roman Catholic Archbishop Marcel Lefebvre and Bishop Antonio de Castro
Mayer published Joint Declaration Against Assisi, again deploring the weakening of the
Catholic faith by Vatican leaders under the influence of the Second Vatican Council.
1987/06/27 - UN  Convention against Torture and Other Cruel, Inhuman or Degrading
Treatment or Punishment, drafted in 1984, signed 1985, entered into force.
1988/11/04 - Congress and President Reagan passed Genocide Convention

Implementation Act of 1987, PL 100-606, 102 Stat. 3045, to implement the International

Convention on the Prevention and Punishment of Genocide. Codified at 18 USC 1091.
1988/11/04 - Congress and President Reagan passed  Health  Omnibus Programs
Extension Act. PL 100-607, 102 Stat. 3048. Section 105 established National Center for
Biotechnology Information under Public Health Service Act (42 USC 286c). Section 156
extended fetal tissue research moratorium imposed in 1985 for two more years. Section
201 outlined and funded HIV-AIDS research under direction of NIH/NIAID/Fauci (42 USC
300cc). Section 256 increased funding for the Public  Health  Emergencies Fund to $45
million (42 USC 247d).
1988/11/23 - Congress and President Reagan passed Robert T. Stafford Disaster Relief
and Emergency Act. PL 100-707,  100 Stat. 4689. Amended 1974 Disaster Relief Act,
FEMA law; redefined ‘emergency’ and ‘major disaster;’ established procedures for
Presidential disaster and emergency declarations, DOD domestic deployment of military
and more. Codified at 42 USC 5121.
1989/12/19 - Congress and President George H.W. Bush passed Omnibus Budget
Reconciliation Act. PL 101-239,  103 Stat. 2106. Section 6601 amended Vaccine Injury
Compensation Program, set up special master program.

1990-1999 - Presidents George H.W. Bush, William J. Clinton

 
 

1990/05/22 - Congress and President Bush passed Biological Weapons Antiterrorism Act
of 1989. PL 101-298,  104 Stat. 201. Drafted by Francis Boyle to bring US into
compliance with 1975 UN convention. Establishing as  criminal, acts of those who
"knowingly develops, produces, stockpiles, transfers, acquires, retains, or possesses any
biological agent, toxin, or delivery system for use as a weapon, or knowingly assists a
foreign state or any organization to do so,” and defined 'for use as a weapon' to “not
include the development, production, transfer, acquisition, retention, or possession of any
biological agent, toxin, or delivery system for prophylactic, protective, or other peaceful
purposes.” Codified at 18 USC 175.
1990/12/21 - HHS Interim Final Rule: Informed Consent for Human Drugs and Biologics;
Determination that Informed Consent is Not Feasible - 55 Federal Register 52814
1991 Common Rule governing research on human subjects.
1992/06/03 - United Nations opened UN Conference on Environment and Development,
commonly called the Earth Summit, in Rio de Janeiro, Brazil.
179 participating nations adopted  Agenda 21 (later renamed Agenda 30), laying out
plans for depopulation, elimination of private property, and elimination of borders and
national sovereignty. Implicitly defined living human beings as biological weapons of
mass destruction, against which lethal chemical and biological agents could be construed
as ‘protective’ and ‘prophylactic’ and therefore exempt from 1975 UN Convention on
Prohibition of Biological Weapons. UN Framework Convention on Climate Change
opened for nation-state signatories to sign.
1992/07/10 - Congress and President Bush passed Alcohol, Drug Abuse,
Mental Health Administration (ADAMHA) Restructuring Act. PL 102-321,  106 Stat. 323.
Expanded drug abuse prevention and treatment programs; reorganized HHS
subdivisions.
1992/10/27 - Congress and President Bush passed Preventative  Health  Amendments.
PL 102-531, 106 Stat. 3504. Changed name from Centers for Disease Control to Centers
for Disease Control and Prevention.
1993/06/10 - Congress and President Clinton passed National Institutes
of  Health  Revitalization Act, PL 103-43,  107 Stat. 122. Reorganized and expanded
research programs; reversed moratorium on fetal tissue research.
1993/11/16 - Congress and President Clinton passed Religious Freedom Restoration Act.
PL 103-141,  107 Stat. 1488. Affirmed Constitutional protections for free exercise of
religion under First Amendment. Related to military personnel requests for religious
exemptions from vaccine mandates, not accepted by DOD. Codified at 42 USC 2000bb.
1993/11/30 - Congress and President Clinton passed NDAA for FY1994, PL 103-
160,  107 Stat. 1547. Section 1703 related to DOD reporting to Congress on chemical
and biological weapons testing programs. Codified at 50 USC 1523. Amended
11/18/1997 and 10/17/2006. Repealed 12/23/2016, effective 12/31/2021?? , Also
authorized DOD to “enter into agreements with Secretary of HHS to provide support for
vaccination programs...in the US through use of the excess peacetime biological
weapons defense capability of the DOD.” Codified at 50 USC 1524.
1994/03/21 - United Nations  Framework Convention on Climate Change  entered into
force. 
1994/09/05 - United Nations opened the International Conference on Population and
Development in Cairo, Egypt. 179 nation-states signed on to a 20-year Programme of
Action for depopulation, which was extended in 2010 to cover 2014-2034.
1994/09/13 - Congress and President Clinton passed Violent Crime Control and Law
Enforcement Act (Clinton Crime Bill). PL 103-322, 108 Stat. 1796. Expanded American
prison state, by expanding predicates for incarcerating nonviolent civilians for long
sentences, increasing funding for prison construction/operation, and law enforcement
officers.
1994/12/08 - Rockefeller Senate Report on US government chemical and biological
weapons research, development, testing and deployment programs. S.Prt. 103-97.
1995 - Launch of World Trade Organization, update to 1947 General Agreement on
Trade and Tariffs.
1996/02/10 - Congress and President Clinton passed National Defense Authorization Act
for FY96. PL 104-106, 110 Stat. 443. Section 1061(k) repealed 50 USC 1511 as adopted
in 1977 and amended in 1982, eliminating requirement that DOD report to Congress on
chemical and biological weapons experiments conducted on military personnel.
1996/04/24 - Congress and President Clinton passed Antiterrorism and Effective Death
Penalty Act; Illegal Immigration Reform and Immigrant Responsibility Act; Prison
Litigation Reform Act. PL 104-132.  110 Stat. 1214. Section 521(a) prohibited DOD
chemical and biological weapons testing in urban and suburban areas, codified at 18
USC 2332C. That provision was repealed in 1998. Also related to court stripping:
Congress passing laws to remove federal courts’ oversight power regarding legislative
and executive acts, eliminate checks and balances.  See  ACLU report, Oct.
2001,  Upsetting Checks and Balances: Congressional Hostility Toward the Courts in
Times of Crisis.
1996/12/17 - UN Comprehensive Convention on International Terrorism opened for
negotiation by  resolution 51/210 forming ad hoc committee; subsequently deadlocked
over definition of terrorism.
1997/04/29 - UN  Convention on the Prohibition of the Development, Production,
Stockpiling and Use of Chemical Weapons and on their Destruction  entered into force,
after drafting in 1992 and signing in 1993.
1997/11/18 - Congress and President Clinton passed National Defense Authorization Act
for FY98 - PL 105-85, 111 Stat. 1915. Section 1078, “Restrictions on the use of human
subjects for testing of chemical or biological agents,” repealed and replaced a 1977
section of 50 USC Chapter 32, the Chemical and Biological Warfare Program. The 1977
provision (50 USC 1520) had added a requirement that DOD report to Congress about
DOD human experimentation programs. In 1997, Congress replaced 1520 with 1520a,
purportedly to prohibit DOD conducting experiments on soldiers without the individual
soldiers informed consent. It was passed by Congress in response to public outrage over
injuries and deaths caused by mandated anthrax injections of soldiers during and after
the 1991 Gulf War. However, the authority for federal government experimentation on
non-consenting human beings continued; Congress simply transferred the program to
the Food Drug and Cosmetics Act, 21 USC 360bbb (see below, passed three days after
the NDAA) under declared emergency situations (Emergency Use Authorizations/EUA).
1997/11/21 - Congress and President Clinton passed Food and Drug Administration
Modernization Act - PL 105-115,  111 Stat. 2296. Added new section to Federal Food
Drug and Cosmetics Act to expand access to investigational drugs and devices during
emergency situations. Codified at 21 USC 360bbb - “Expanded Access to Unapproved
Therapies and Diagnostics”. This was the beginning of the Emergency Use
Authorization/EUA framework that culminated in the American government’s
psychological, social and economic coercion program aimed at universal injection of all
American citizens with products marketed as Covid-19 vaccines, operational from mid-
2020 to the present.
1998/03 -  Washington DC tabletop exercise  on smallpox epidemic. Used for political
cover six months later to establish Strategic National Stockpile of US-government-
controlled chemical and biological weapons, disguised as ‘vaccines’ and other
‘pharmaceutical’ products.
1998/10/17 - Congress and President Clinton passed National Defense Authorization Act
for FY1999. PL 105-261, 112 Stat. 1920. Section 1401.
1998/10/21 - Congress and President Clinton passed Omnibus Consolidated and
Emergency Supplemental Appropriations for FY1999 - PL 105-277, 112 Stat. 2681-358.
Title II established the National Pharmaceutical Stockpile, later renamed the Strategic
National Stockpile. Appropriated $51,000,000, “to remain available until expended…for
pharmaceutical and vaccine stockpiling activities at the Centers for Disease Control and
Prevention.” Division I, Chemical Weapons Convention Implementation Act of 1998,
established prohibitions on chemical weapons. Codified at  18 USC 229  and  22 USC
6701.
1999/09/17 - Death of Jesse Gelsinger from early gene therapy trial.
1999/09/30 - President Clinton signed
Executive Order 13139: Improving Health Protection of Military Personnel Participating in
Particular Military Operations. Authorized administration of experimental, FDA-
unapproved vaccines to members of the armed forces without informed consent.  64
Federal Register 54175
1999/10/05 - HHS Interim Final Rule - Human Drugs and Biologics; Determination That
Informed Consent Is NOT Feasible or Is Contrary to the Best Interests of Recipients;
 Revocation of 1990 Interim Final Rule; Establishment of New Interim Final Rule.  64
Federal Register 54180
1999/11 - Population-control zealot  Bill Gates launched GAVI  (Global Alliance for
Vaccines and Immunizations) with $750 million investment from  Bill  & Melinda Gates
Foundation. Public-private partnership organization develops, tests, manufactures and
deploys pharmaceutical products in low and middle-income countries.

2000 - 2009 - Presidents William Clinton, George W. Bush, Barack H. Obama

 
 

2000/09 - FDA approved RU-486, mifepristone pill for use to terminate pregnancies:
chemical abortion drug.
2000/09 - Project for the New American Century published  Rebuilding America’s
Defenses  report. “Advanced forms of biological warfare that can ‘target’ specific
genotypes may transform biological warfare from the realm of terror to a politically useful
tool.”
2000/11/13 - Congress and President Clinton passed Public  Health  Improvement Act -
PL 106-505,  114 Stat. 2314. Title I, Public  Health  Threats and Emergencies Act,
reworked and expanded Section 319 of Public  Health  Service Act, 42 USC 247d (the
Public  Health  Emergencies section first added in 1983). Appropriated funding and
established a working group on bioterrorism ‘countermeasures’ research and
development.
2001/09/11 - Terrorist airplane attacks on World Trade Center and Pentagon.
2001/09/14 - George W. Bush signed Proclamation 7463,  Declaration of National
Emergency by Reason of Certain Terrorist Attacks,  under 1975 National Emergencies
Act.  Renewed every year since, most recently by Biden in Sept. 2021.  66 Federal
Register 48199
2001/09/18 - 2001/10/09 - Anthrax attacks on US Congress and media organizations.
2001/09/18 - Congress and President Bush passed Authorization for Use of Military
Force. PL 107–40; 115 Stat. 224. Passed under the 1973 War Powers Act, 50 U.S. Code
§ 1541, and construed as putting the United States in a permanent state of war (Global
War on Terror) with no limitations in time or geographically.
2001/09/23 - President Bush signed Executive Order 13224, blocking property ownership
and prohibiting transactions with persons who commit, threaten to commit or support
terrorism. List maintained by Office of Foreign Assets Control, US Dept. of Treasury.
2001/10/23 - Model State Emergency Health Powers Act  promulgated by CDC and the
Center for Law and the Public's Health at Georgetown and Johns Hopkins Universities,
“structured to reflect 5 basic public  health  functions to be facilitated by law: (1)
preparedness, comprehensive planning for a public  health emergency; (2) surveillance,
measures to detect and track public  health  emergencies; (3) management of property,
ensuring adequate availability of vaccines, pharmaceuticals, and hospitals, as well as
providing power to abate hazards to the public's health; (4) protection of persons, powers
to compel vaccination, testing, treatment, isolation, and quarantine when clearly
necessary; and (5) communication, providing clear and authoritative information to the
public.”
2001/10/26 - Congress and President Bush passed Uniting and Strengthening America
by Providing Appropriate Tools Required to Intercept and Obstruct Terrorism (USA
PATRIOT) Act - PL 107-56, 115 Stat. 272. Amended 18 USC 2331 - Definitions section of
18 USC 113B - Terrorism - to add “domestic terrorism,” defined as activities that “(A)
involve acts dangerous to human life that are a violation of the criminal laws of the United
States or of any State; (B) appear to be intended—(i)to intimidate or coerce a civilian
population; (ii) to influence the policy of a government by intimidation or coercion; or (iii)
to affect the conduct of a government by mass destruction, assassination, or kidnapping;
and (C) occur primarily within the territorial jurisdiction of the United States.” There
is  plenty of evidence to prosecute and convict Fauci, Baric, Gates, Daszak and others
under this criminal statute. However, this is also why the conspirators used the FBI to
infiltrate the January 6, 2021 Washington DC election protests, to ensure breach of the
Capitol and subsequent arrests and indefinite detentions of non-violent trespassers, to
create predicates to steer and shape national panic about domestic terrorism exclusively
defined as civilians challenging the legitimacy of government officials and acts, to steer
public anger and distrust away from government agents killing, maiming and imprisoning
civilians.
2002/06/12 - Congress and President Bush passed Public  Health  Security and
Bioterrorism Preparedness and Response Act - PL 107-188,  116 Stat. 594. Major
amendments to Public  Health  Service Act (42 USC 201) and Federal Food Drug and
Cosmetics Act (21 USC 9). This law fully constructed and expanded funding for the
federal government’s domestic bioterrorism apparatus headquartered at the CDC,
disguising it as a program to protect Americans from non-state actors. Sections included
National Preparedness and Response Planning, Coordinating, and Reporting; Strategic
National Stockpile; Development of Priority Countermeasures (i.e. fast-tracking approval
of drugs and devices without standard safety testing, efficacy testing, and regulatory
compliance); Improving State, Local, and  Hospital  Preparedness for and Response to
Bioterrorism and Other Public  Health  Emergencies; Emergency Authorities (i.e. federal
quarantine power); Controls on Dangerous Biological Agents and Toxins (Title II, Subtitle
B:  Agricultural Bioterrorism Protection Act of 2002); Safety and Security of Food and
Drug Supply; Drinking Water Security and Safety. Coincidentally also in 2002, HHS-NIH-
funded (grant no. AI23946-08)  University  of North Carolina researcher and Fauci
colleague Ralph Baric filed a  US patent (7,279,372)  on methods to make bat
coronaviruses more lethal to humans, noting that “the US government has certain rights
to this invention.” More on that.
2002/11/25 - Congress and President Bush passed Homeland Security Act - PL 107-
296,  116 Stat. 2135. Established Department of Homeland Security as a cabinet-level
administrative arm of the executive branch. Expanded militarization of domestic
surveillance and law enforcement. Title V: established a Directorate of Emergency
Preparedness and Response within Department of Homeland Security, headed by an
Undersecretary. Strengthened crosslinks between DHS and other federal
agencies:  Health  and Human Services, Federal Emergency Management Agency
(FEMA), Department of Defense, Department of Justice and Department of Agriculture,
to build and operate a public-health-predicated martial law system.
2003/04/04 - Congressional hearing held on Project Bioshield: Contracting for the Health
and Security of the American Public. Congress members discussed authorizing HHS to
waive informed consent during declared emergencies. (06/14/2022 Bailiwick post  with
partial transcript.)
2003/04/04 - President Bush signed Executive Order 13295 added symptomatic SARS to
list of quarantinable communicable diseases, authorizing HHS to order apprehension and
indefinite detention of Americans for contracting common respiratory illnesses under 42
USC 264(b) and 42 CFR 70.6. 68 Federal Register 17255.
2003/09/16 -  Model State Public Health Act  published by Johns Hopkins, Georgetown
and CDC, working through Turning Point Initiative/Turning Point National Collaborative.
Slightly less aggressive form of Model State Emergency Health Powers Act circulated in
October 2001.
2003/11/24 - Congress and President Bush passed National Defense Authorization Act
for FY2004. PL 108-136, 117 Stat. 1392. Section 1603(a), created 21 USC 360bbb-3 -
“Section 564 - Authorization for Medical Products for Use in Emergencies” under the
EUA part of the Federal Food Drug and Cosmetics Act as amended in 1997 to add 21
USC 360bbb “Expanded Access to Unapproved Diagnostics and Therapies.” At Section
1603(b)(1), Congress added Section 1107a to the military code after 10 USC 1107,
authorizing the US President to waive informed consent rights of military personnel
during declared emergencies and redefining the meaning of the right to be “informed of
an option to accept or refuse administration of a product.”
2003/12/22 - US federal court in  Doe v. Rumsfeld, 297 F Supp. 2d 119  (DDC 2003)
addressed informed consent (10 USC 1107) and Presidential waivers (10 USC 1107a) in
the anthrax vaccination campaign context. Federal court enjoined DOD from overriding
service members informed consent requirements with the experimental Anthrax vaccine.
Eight days later, FDA fully approved the Anthrax vaccine. That FDA decision was
vacated by the Court 10/27/2004 in Rumsfeld II, 341 F. Supp. 2d 1 (D.D.C. 2004). The
injunction was expanded to cover the vaccine after being granted EUA status
in Rumsfeld III. 2005 WL 774857 (D.D.C. April 6, 2005)
2004/07/21 - Congress and President Bush passed Project Bioshield Act. PL 108-
276,  118 Stat. 835. Amendments to Public  Health  Service Act and Federal Food Drug
and Cosmetics Act. Nullified informed consent principles under US law. Amended and
expanded 21 USC 360bbb on authorization for investigational drugs and devices to be
used in emergencies (Emergency Use Authorization). Established program for ‘qualified
countermeasure’ research, procurement, contracting, manufacture, use and liability
exemptions. Expanded authority of NIAID Director (Fauci). Appropriated $640,000,000
for the Strategic National Stockpile for FY2002, $590,000,000 for smallpox vaccine
development for FY2002, and $5,593,000,000 for “procurement of security
countermeasures.” Expanded HHS power to subject citizens to involuntary relocation and
indefinite detention on communicable disease predicates. Expanded coordination among
Secretary of  Health  and Human Services, Secretary of Defense and Secretary of
Homeland Security.
2005/04/01 - President Bush signed Executive  Order  13375, adding symptomatic
influenza to list of quarantinable communicable diseases, authorizing HHS Secretary to
use force to apprehend and detain people under 42 USC 264(b) and 42 CFR 70.6..  64
Federal Register 17299.
2005/04/02 - Death of Roman Catholic Pope John Paul II. After conclave, Pope Benedict
XVI took the papacy 04/19/2005.
2005/07/05 - HHS FDA Draft Guidance Re: Emergency Use Authorization of Medical
Products. 70 FR 38689.
2005/09/15 - World  Health  Assembly adopted  World Health Organization International
Health Regulations 2005 revisions. Entered into force 06/15/2007.
2005/12/30 - Congress and President Bush passed Department of Defense, Emergency
Supplemental Appropriations to Address Hurricanes in the Gulf of Mexico, and Pandemic
Influenza Act - PL 109-148,  119 Stat. 2818, Division C at last 14 pages:  Public
Readiness and Emergency Preparedness (PREP) Act.  Amended
Public  Health  Service Act. Established power of Secretary of  Health  and Human
Services, during self-declared public health emergency under Section 319, to unilaterally
issue declarations recommending “manufacture, testing, development, distribution,
administration, or use of one or more covered countermeasures.” Codified at 42 USC
247d-6d(b). Added more detail on liability shields for pandemic and epidemic products
and security countermeasures. Set pre-suit  hurdle requiring HHS to first bring claims
against defendants, and bar private claims until after HHS claims resolved, if and only if
defendant found liable. Set liability standard at willful misconduct, “establishing a
standard…more stringent than negligence in any form or recklessness,” requiring proof
defendant 1) intentionally engaged in misconduct 2) proximate to victim’s injury or death.
Established just-following-orders defense for vaccinators and others in the chain of
distribution. Established court-alternative, tax-and-debt-funded Covered Countermeasure
Process Fund, similar to Vaccine Injury Compensation Fund established in 1986 for
products on childhood vaccine schedule. Another provision of the DOD Supplemental
Emergency Appropriation funded the Public Health and Social Service Emergency Fund
(PHSSEF), a slush fund under the control of the Secretary of  Health  and Human
Services, with $3.3 billion to start.
2006/06/07 - HHS-FDA Interim Final Rule, Medical Devices; Exception From

General Requirements for Informed Consent. 71 Federal Register 32827

2006/09 - Department of Justice published report:  Role of Law Enforcement in Public
Health Emergencies: Special Considerations for an All-Hazards Approach. “Depending
on the threat, law enforcement’s role may include

enforcing public health orders (e.g., quarantines or travel restrictions),

securing the perimeter of contaminated areas, securing health care

facilities, controlling crowds, investigating scenes of suspected biological

terrorism, and protecting national stockpiles of vaccines or other

medicines.”
2006/10/17 - Congress and President Bush passed NDAA/John Warner Defense
Authorization Act for FY2007 - PL 109-364, 120 Stat. 2095. Section 1076 amended 1807
Insurrection Act, (10 USC 333, renumbered as 10 USC 253), providing exemptions to
1878 Posse Comitatus Act, to expand the authority of federal government to deploy US
military on American soil against American citizens during “natural disaster, epidemic, or
other serious public  health  emergency, terrorist attack or incident, or other condition in
any State or possession of the United States.” Repealed in NDAA for FY2008. Passed
again in NDAA for FY2012.
2006/11/28 - HHS FDA Guidance: Gene Therapy Clinical Trials - Observing Subjects for
Delayed Adverse Effects
2006/12/19 - Congress and President Bush passed Pandemic and All-Hazards
Preparedness Act. PL 109-417,  120 Stat. 2878. Fulfilled many of the requirements of
the  World Health Organization International Health Regulations of 2005, by further
consolidating and centralizing power in federal Health and Human Services Secretary’s
hands. Created new HHS department, led by new Assistant Secretary for Preparedness
and Response (counterpart to the DHS Director of Emergency Preparedness and
Response position created in 2002). Established rules for coordination among HHS,
Secretary of Defense, Secretary of Veterans Affairs, Secretary of Transportation and “any
other relevant federal agency.” Established national framework subordinating state,
county, tribal and local public health  and law enforcement systems to federal agencies.
Expanded surveillance programs. Clarified definitions of qualified countermeasure,
security countermeasure, and infectious disease for purposes of 2004 Project Bioshield
Act. Established Biomedical Advanced Research and Development Authority (BARDA)
division under HHS, “to facilitate a broad-based approach to emergency medical
countermeasure-related activities,” including $1,070,000,000 appropriation. Tools
included HHS authority to limit competition among manufacturers of pandemic products
as defined under 2004 Project Bioshield Act.
2007/01/15 - Congress and President Bush passed National Institute of  Health  Reform
Act - PL 109-482, 120 Stat. 3675. Reorganization, consolidation of power and funding.
2007/05/04 - President Bush issued  National Security Presidential Directive 51. US
Government Continuity of Operations policy.
2007/06/15 -  World Health Organization International Health Regulations, 2005
Amendments, entered into force.
2007/07/01 - HHS FDA  Guidance - Emergency Use Authorization of Medical
Products.  71 FR 41083. Finalized draft guidance published in Federal Register
07/05/2005.
2007/07/07 - Roman Catholic Pope Benedict XVI issued  Summorum Pontificum,
affirming the right of Catholic priests and faithful to celebrate the pre-1962, Traditional
Latin Mass.
2007/09/27 - Congress and President Bush passed Food and Drug Administration
Amendments Act of 2007. PL 110-85,  121 Stat. 823. Expanded FDA power over new
product authorizations and post-marketing surveillance.
2007/12/28 - HHS Interim Final Rule - FDA Exceptions or Alternatives to Labeling
Requirements for Products Held by the Strategic National Stockpile. Effective same
day. 72 FR 73589.
2008/01/28 - Congress and President Bush passed National Defense Authorization Act
for FY2008. PL 110-181,  122 Stat. 325. Section 1068 repealed 2007 amendments to
Insurrection Act which had expanded exemptions to 1878 Posse Comitatus Act limits on
US Presidents’ power to deploy the military domestically. Amendments passed again in
NDAA for FY2012, again giving President power to deploy military domestically.
2008/07 - DOJ-CDC published A Framework for Improving Cross-Sector Coordination for
Emergency Preparedness and Response. Merging public health and law enforcement.
2009 H1N1 outbreak, first mass vaccination campaign since 1976 swine flu outbreak.
2009/11/18 - HHS FDA Workshop Summary:  Medical Countermeasures Dispensing:
Emergency Use Authorization and the Postal Model. “At the workshop, participants noted
that EUA has a broader use beyond enabling the use of an unapproved product or
extending the use of an approved product to populations for which it was not approved.
In particular, it can also be used to address labeling requirements and other challenges
that arise because of constraints inherent in a public  health  response. ‘From a legal
perspective, there are a lot of situations where EUA helps get past all those
 requirements,’ said [Susan E. Sherman, J.D., M.S., is a senior attorney with
the Office of the General Counsel, HHS] ‘You can change the labeling. You can change
the information. You can change the dosage. You can give it to populations for which
wasn’t approved.’ ”

2010-2019 - Presidents Barack H. Obama, Donald J. Trump

 
 

2010/03/23 - Congress and President Obama passed Patient Protection and Affordable
Care Act (ObamaCare). PL 111-148, 124 Stat. 119. Title VII, Biologics Price Competition
and Innovation Act of 2009, related to the legal, approval/authorization, labelling and
marketing differences among ‘biosimilars,’ BLA (Biologics License Application) products,
and EUA products.
2010/07/02 - President Obama signed Executive Order 13546, Optimizing the Security of
Biological Select Agents and Toxins in the United States. 75 Federal Register 39439.
2011/01 - HHS FDA Guidance for Industry: Potency Tests for Cellular and Gene Therapy
Products
2011/06/24 - HHS-FDA Final Rule:  Medical Devices; Exception From General
Requirements for Informed Consent. 76 Federal Register 36989.
2011/09/16 - Congress and President Obama passed Leahy Smith America Invents Act.
PL 112-29, 125 Stat. 340. Section 33 limited the authority of the US patent office under
35 USC 101, by prohibiting issuing of patents “directed to or encompassing a human
organism.” Related to 1980  Chakrabarty  and 2013  Myriad  Supreme Court precedents
authorizing patents on genetically-modified living organisms and modified genetic
material, and government-ordered mRNA and DNA spike protein Covid injections that
reverse-transcribed genetic material into human genome of recipients.
2011/12/31 - Congress and President Obama passed National Defense Authorization Act
for FY2012 - PL 112-81, 125 Stat. 1298. Section 1021 codified authority for US President
to  order  military arrest and indefinite detention of American civilians without charge or
trial under 10 USC 801 et seq. (Uniform Code of Military Justice), to the extent the 2001
Authorization for Use of Military Force, passed under the 1973 War Powers Act, (50 U.S.
Code § 1541) is construed as putting the United States in a permanent state of war
(Global War on Terror) and the national emergency first declared by President Bush in
2001 is extended. It has been extended, every year since.
2012/07/09 - Congress and President Obama passed Food and Drug Administration
Safety and Innovation Act. PL 112-144,  126 Stat. 993. Amendments to Federal Food,
Drug, and Cosmetic Act regarding user-fee programs for prescription drugs and medical
devices, generic drugs and biosimilars, and for other purposes.
2013/01/02 - Congress and President Obama passed National Defense Authorization Act
for FY2013. PL 112-239, 126 Stat. 1957. Section 1078 “modernized” Smith-Mundt Act of
1948 to authorize domestic deployment of propaganda by the US government, on the
American population. Propaganda used with tremendous effect on US population to instill
fear and promote behavioral compliance with government orders.
2013/01/29 - Congress and President Obama passed Disaster Relief Appropriations Act.
PL 113-2, 127 Stat. 4. Division B, Sandy Recovery Act: most major FEMA overhaul since
1988 Robert T. Stafford Act.
2013/02/28 - Roman Catholic Pope Benedict XVI resigned. After conclave, the papacy of
Pope Francis began 03/13/2013.
2013/03/13 - Congress and President Obama passed Pandemic and All-Hazards
Preparedness Reauthorization Act. PL 113-5, 127 Stat. 161. Renewed and updated 2006
Pandemic and All-Hazards Preparedness Act, with amendments to Public Health Service
Act and Federal Food Drug and Cosmetics Act. Added sections 564A and 564B to the
FDCA to further authorize emergency use of approved products in emergencies and
products held for emergency use. Amended definitions of covered countermeasures and
qualified pandemic and epidemic products in Section 319F-3 of PHSA (2005 PREP Act
provisions). Extended definitions to include products or technologies intended to enhance
the use or effect of a drug, biological product, or device used against the pandemic or
epidemic or against adverse events from these products.
2013/06/13 - US Supreme Court ruled on Association for Molecular Pathology v. Myriad
Genetics,  539 US 576, in favor of the biotech corporation and the federal government,
finding that naturally-occurring DNA is not patentable, but synthetic cDNA is patentable,
under 35 USC 101. Implicates mRNA/DNA injections administered on global population
starting in December 2020, reverse-transcription into human genome, and whether
injected humans are chattel property of Covid-19 injection patent-holders within US
government/DOD, Pfizer, Moderna, AstraZeneca and Janssen.
2014/07/31 - President Obama signed Executive  Order  13674, adding asymptomatic,
suspected SARS to list of quarantinable communicable diseases under  42 USC
264(b) and 42 CFR 70.6. 79 Federal Register 75461
2014/08/19 - HHS FDA Guidance:  Decisions for Investigational Device Exemption
Clinical Investigations. Related to federal government’s position on legal status and
regulatory control differences between Emergency Use Authorization (EUA) products,
Investigational New Drugs (IND) and Investigational Device Exemptions (IDE).
2015/04/16 - Congress and President Obama passed Medicare Access and CHIP
Reauthorization (MACRA) Act. PL 114-10, 129 Stat. 87. Largest changes to health  care
system since 2010 ObamaCare. Section 511 directed HHS to clarify how changes to
human subjects protections under 1991 Common Rule would apply to Medicare and
Medicaid “clinical data registries.” Related to ‘real world evidence’ with no legal
protections for human subjects, replacing traditional clinical trial procedures that did have
legal protections for human subjects. Codified at…
2015/06 - HHS FDA Guidance:  Considerations for the Design of Early-Phase Clinical
Trials of Cellular and Gene Therapy Products
2015/08 - HHS FDA Guidance:  Design and Analysis of Shedding Studies for Virus or
Bacteria-Based Gene Therapy and Oncolytic Products
2015/11/25 - Congress and President Obama passed National Defense Authorization Act
for FY-2016. PL 114-92,  129 Stat. 893. Section 815 added ‘prototype’ procurement
contracting language (Other Transactional Authority - OTA), authorizing Department of
Defense to contract with pharmaceutical corporations to produce bioweapons labeled as
medical countermeasures or security countermeasures. Used to contract for production
of ‘Covid-19 vaccine’ bioweapons in 2020, through Medical CBRN [Chemical Biological
Radiological Nuclear] Defense Consortium program members. Codified at 10 USC
2371b, renumbered 10 USC 4022 effective 01/01/2021. First two posts on this
topic: 05/25/2022 and 05/26/2022.
2016/09/21 - HHS Final Rule - HHS Clinical Trials Registration and Results. 81 Federal
Register 64981
2016/10/17 - Congress and President Obama passed National Defense Authorization Act
for FY2017. PL 114-328, 130 Stat. 2000. 10 USC 111 note at 130 Stat. 2400
2016/10/24 - HHS Workshop Summary -  The Nation's Medical Countermeasure
Stockpile: Opportunities to Improve the Efficiency, Effectiveness, and Sustainability of the
CDC Strategic National Stockpile.
2016/11/04 - President Obama signed  Executive Order 13747:  Advancing the
Global  Health  Security Agenda to Achieve a World Safe and Secure from Infectious
Disease Threats
2016/12/13 - Congress and President Obama passed 21st Century Cures Act (Cures Act
1.0) - PL 114-255, 130 Stat. 1033. Updated and expanded Public Health Service Act “to
accelerate the discovery, development, and delivery of 21st century cures.” Section 3022
authorized ‘real world evidence’ instead of clinical trials as grounds for FDA authorizing
general use of experimental products, transforming Americans into human subjects and
our communities into unmonitored, unregulated experimental test sites. Sections 3023
and 3024 granted broad authority for HHS Secretary to waive or alter human subject
protections and informed consent requirements, by transferring each individual human
subject’s risk-benefit assessment authority to the HHS Secretary, who can preemptively
decide, for all subjects collectively, without knowledge of individual  health  conditions or
conscientious beliefs, and without the subjects’ knowledge or consent, that risk is
‘minimal.’ Codified at…
2016/12/23 - Congress and President Obama passed National Defense Authorization Act
for FY2017. PL 114-328, 130 Stat. 2509. Established DOD Defense Security Cooperation
Agency (DSCA) and Director of DSCA, with authority to coordinate and synchronize US
military with foreign military forces, and conduct domestic military campaigns in violation
of the 1878 Posse Comitatus Act. Codified at 10 USC 382.
2017/01/13 - HHS  FDA Guidance:  Emergency Use Authorization of Medical Products
and Related Authorities  (Update/revision to 07/01/2007 version). Related to federal
government’s position on legal status and regulatory control differences between
Emergency Use Authorization (EUA) products, Investigational New Drugs (IND) and
Investigational Device Exemptions (IDE).
2017/01/19 - HHS Final Rule - Federal Policy for the Protection of Human Subjects. 82
FR 7149. Joint rule by 16 federal agencies, subsequently adopted by other agencies.
Revised  1991 Common Rule, which had been developed based on  1947 Nuremberg
Code and 1978 Belmont Report.
2017/01/19 HHS Final Rule -  Control of Communicable Diseases Final Rule. 82 FR
6890. Set up regulations governing apprehension and detention of American people on
public health quarantine pretexts.
2017/01/23 - Department of Homeland Security published  Biological Incident Annex to
the Response and Recovery Federal Interagency Operational Plans. At p. 70, stated that
10 USC 382 “permits Department of Defense to provide support to the Department of
Justice under certain circumstances in emergency situations involving Weapons of Mass
Destruction, including biological weapons and materials.”
2017/07/25 - HHS  FDA Guidance: IRB Waiver or Alteration of Informed Consent for
Clinical Investigations Involving No More Than Minimal Risk to Human Subjects
2017/08 - HHS  FDA Guidance:  Use of Real-World Evidence to Support Regulatory
Decision-Making for Medical Devices
2017/08/18 - Congress and President Trump passed FDA Reauthorization Act - PL 115-
52. 131 Stat. 1005
2017/10 - Johns Hopkins  University  Center for  Health  Security exercise and
report,  SPARS Pandemic, 2025-2028, A Futuristic Scenario for Public Health Risk
Communicators. Chapter 13 covered how government and corporate PR representatives
should handle “anti-vaccine” messages. Chapter 17 covered how they should manage
public awareness and anger about vaccine injury.
2017/12/12 - Congress and President Trump passed National Defense Authorization Act
FY 2018 - PL 115-91,  131 Stat. 1283. Section 716 added subsection (d) to 10 USC
1107a, re: EUA product use in military.  But see  FDCA amendment, PL 115-92 (below)
passed same day, which immediately repealed 10 USC 1107a(d) while adding new
FDCA section on military use of EUAs.
2017/12/12 - Congress and President Trump passed Act to amend FDCA EUA statute,
21 USC 360bbb-3. PL 115-92, 131 Stat. 2023. Provided for “Additional Emergency Uses
for Medical Products to Reduce Deaths and Severity of Injuries Caused by Agents of
War.” Codified at…
2018/01 - FEMA published Pandemic Crisis Action Plan/PanCAP.
2018/06/19 - HHS Final Rule - Federal Policy for the Protection of Human Subjects: Six
Month Delay of the General Compliance Date of Revisions While Allowing the Use of
Three Burden-Reducing Provisions During the Delay Period. 83 Federal Register 28497
2018/06/19 -  Biodefense in the Age of Synthetic Biology  published by US National
Academies of Sciences, Engineering, Medicine.
2018/10/05 - Congress and President Trump passed Federal Aviation Administration
Reauthorization Act. PL 115-254, 132 Stat. 3186. Division D, Disaster Recovery Reform
Act, another major FEMA update.
2018/10/09 - Johns Hopkins  University  Center for  Health  Security published
report Technologies to Address Global Catastrophic Biological Risks, on ‘self-spreading
vaccine’ technology, informed consent challenges of same, and ‘self-amplifying mRNA
vaccines.’
2019/02/11 - President Trump signed  Executive Order 13859:  Maintaining American
Leadership in Artificial Intelligence. Directed and prioritized federal agency collaboration
with industry for AI research and development.
2019/05/22 -  Congressional Research Service Opinion: An Overview of State and
Federal Authority to Impose Vaccination Requirements by Wen W. Shen
2019/06/11 - President Trump signed Executive  Order  13874:  Modernizing the
Regulatory Framework for Agricultural Biotechnology Products.  84 Federal Register
27899.
2019/06/24 - Congress and President Trump passed Pandemic and All-Hazards
Preparedness and Advancing Innovation Act - PL 116-22,  133 Stat. 905. Amended
Public  Health  Service Act (42 U.S.C. 201), further consolidating federal power in HHS
Secretary’s hands during public  health  emergencies, further merging public  health  and
law enforcement systems, and further subordinating state, tribal, county and municipal
governments and American civilians to direct federal control.
2019/09/19 - President Trump signed  Executive Order 13887:  Modernizing Influenza
Vaccines in the United States to Promote National Security and Public Health. Directed
and prioritized federal agency collaboration with industry for rapid-deployment
mRNA/DNA/LNP/nanotech bioweapon platforms misclassified as
public health protection.
2019/10/04 - 10/19 - Roman Catholic Pope Francis hosted pagan Pachamama/Gaia
worship ceremony in Vatican Garden, at Basilica of St. Peter, and Santa Maria
 Traspontina  Church, and during Way of the Cross, until angry Catholics seized pagan
statues and threw them into Tiber River.
2019/10/18 - Johns Hopkins Center for Health Security conducted Event 201:
“…a pandemic tabletop exercise that simulated a series of dramatic, scenario-based
facilitated discussions, confronting difficult, true-to-life dilemmas associated with
response to a hypothetical, but scientifically plausible, pandemic...”
2019/12/12 -  Material Transfer Agreement  signed between US  Health  and Human
Services (HHS) National Institutes of  Health  (NIH) National Institute for Allergies
and  Infection  Diseases (NIAID), led by Anthony Fauci,  University  of North Carolina
coronavirus researcher and patent-holder Ralph Baric, and Moderna, for “mRNA
coronavirus vaccine candidates developed and jointly owned by NIAID and Moderna.”

2020 - Present - Presidents Donald J. Trump, Joseph R. Biden

 
 

2020/01/27 -  US Secretary of Health and Human Services Determination that a Public

Health Emergency Exists. Signed Jan. 31, 2020, effective Jan. 27, 2020. Renewed every
90 days since then, most recently Oct. 13, 2022. Also signed a ‘declaration that
circumstances exist justifying the authorization of emergency use of in vitro diagnostics
for detection and/or diagnosis of this novel coronavirus.’ The determination and
declaration were recorded in the Federal Register as taking effect Feb. 4, 2020.  85
Federal Register 7316.
2020/01/30 - WHO Director-General Tedros Adhanom Ghebreyesus  declared Covid-19
outbreak a “public health emergency of international concern,”  (PHEIC) triggering the
legal obligations of WHO member states under the 2005
International  Health  Regulations, to suspend national sovereignty and constitutional
rights of citizens using the implementing domestic statutes and regulations they had
adopted in compliance with the WHO IHR.
2020/02/04 - US Secretary of Health and Human Services Declaration Under the Public
Readiness and Emergency Preparedness Act for Medical Countermeasures Against
COVID–19. 85 Federal Register 15198 (6 pages). Issued March 10, 2020, effective Feb.
4, 2020. Deployment of the domestic bioterrorism program against all American citizens
under Covid-19 pretext.
2020/03/01 - HHS Centers for Medicare and Medicaid Services (CMS)  COVID-19
Emergency Declaration Blanket Waivers for Health Care Providers.
Exempted health care providers from patient care standards and regulations that would
legally apply in non-pandemic circumstances; authorized stripping patients of their rights
to have family members and pastors/rabbis visit them and advocate for them in
the hospital or nursing home; supported hospital demands that law enforcement officers
remove family and pastors from the premises by force; created conditions for  death
protocols of restraint, withheld water  and nutrition, forcible administration of Remdesivir
and forcible connection to ventilators under the ICD-10 codes.
2020/03/06 - Congress and President Trump passed Coronavirus Preparedness and
Response Supplemental Appropriations Act - PL 116-123,  134 Stat. 146. $8.3 billion
to  Health  and Human Services, Centers for Disease Control and Prevention, National
Institute of Health, National Institute of Allergy and Infectious Diseases, Food and Drug
Administration, Small Business Administration, Department of State and US Agency for
International Development, for research and development of vaccines, therapeutics and
diagnostics and other Covid programs.
2020/03/13 - PanCAP Adapted U.S. Government Covid-19 Response Plan.
2020/03/13 - President Trump issued a Stafford Act declaration under the 1988 Stafford
Act, and signed Proclamation 9994,  Declaring a National Emergency Concerning the
Novel Coronavirus Disease (COVID–19) Outbreak,  under the 1975 National
Emergencies Act. Renewed every year since, most recently by Biden in Feb. 2022.  85
Federal Register 15337.
2020/03/18 - Congress and President Trump passed Families First Coronavirus
Response Act - PL 116-127,  134 Stat. 178. $3.5 billion for Covid mass testing,
supplemental nutrition (Department of Agriculture), sick leave, family medical leave, and
unemployment compensation (Department of Labor) programs.
2020/03/24 - HHS Secretary Alex Azar issued Declaration of Emergency Use

Authorization, declaring “that circumstances exist justifying the authorization of

emergency use of medical devices, including alternative products used as

medical devices.” 85 Federal Register 17335.

2020/03/27 - Congress and President Trump passed Coronavirus Aid, Relief, and
Economic Security (CARES) Act - PL 116-136, 134 Stat. 281. 15 USC 9001. $2.2 trillion
in corporate and small business loans, household stupport and unemployment insurance,
tax deferrals, aid to state and local governments, aid to universities and colleges, aid to
K-12 schools, aid to hospitals and veterans programs, airline loans and grants, and $10
billion for “Operation Warp Speed.”
2020/04/24 - Congress and President Trump passed Paycheck Protection Program
and  Health  Care Enhancement Act - PL 116-139,  134 Stat. 620. $75,000,000,000 for
Public  Health  and Social Services Emergency Fund (first funded in 2005), “to remain
available until expended, to prevent, prepare for, and respond to coronavirus,
domestically or internationally” plus $25,000,000,000 for research, development and
deployment of Covid-19 tests.
2020/05/19 -  Advisory Opinion on the PREP Act and the March 10, 2020 Declaration
Under the Act, April 17, 2020, as modified on May 19, 2020, by Robert P. Charrow of
HHS Office of General Counsel. Legal opinion on statutory liability shields.
2020/05/29 - Supreme Court ruled in South Bay United Pentecostal Church v. Newsom,
590 US __, (2020), denying role for federal judiciary in Constitutional review of executive
and legislative acts taken during declared public health emergencies. Semi-reversed on
rehearing, February 2021.
2020/07/20 - DOD-Pfizer Base Agreement, through Advanced Technology International;
2020/07/21 - DOD-Pfizer  Statement of Work, through Advanced Technology
International. Pfizer later argued (04/22/2022,  Jackson v. Ventavia,  Motion to Dismiss)
that “Because of pandemic-related exigencies, the agreement was not a standard federal
procurement contract, but rather a ‘prototype’ agreement executed pursuant to 10 U.S.C.
§ 2371b[.]…The [contract’s Statement of Work] describes a ‘large scale vaccine
manufacturing demonstration’ that imposes no requirements relating to Good Clinical
Practices (‘GCP’) or related FDA regulations.” 10 USC Section 2371 renumbered 10
USC 4022, 01/01/2021
2020/08/26 -  HHS CDC Advisory Committee on Immunization Practices Meeting
Summary Report. At p. 56 - “Dr. Cohn reminded everyone that under an EUA, vaccines
are not allowed to be mandatory. Therefore, early in the vaccination phase individuals will
have to be consented and cannot be mandated to be vaccinated.” [Attorney Johnsen
cited this interpretation of Section 564 in a footnote on p. 7 of her 07/06/2021 slip opinion,
immediately citing the  judge’s 06/12/2021  order  in Bridges v.  Houston  Methodist as
“summarily rejecting” the argument.]
2020/12/27 - Consolidated Appropriations Act - PL 116-260, 134 Stat. 1182. $2.3 trillion
spending bill, including $900 billion for Covid programs.
2021/01/05 - Orange Book Transparency Act - PL 116-290, 134 Stat. 4889. Amendments
to patent law under Federal Food Drug and Cosmetics Act, (21 USC 9)
2021/01/21 - HHS Secretary Norris Cochrane  notifies state governors that federal
government will give 60 days notice  before terminating the '“determination that a
public  health  emergency exists” first issued by HHS Secretary Alex Azar effective
01/27/2020.
2021/03/11 - Congress and President Biden passed American Rescue Plan/Consolidated
Appropriations Act. PL 117-2, 135 Stat. 4. Section 1401, Covid-19 Consumer Protection
Act. Criminalized advocacy of alternative treatments under Federal Trade Commission
provisions.
2021/04/02 -  Congressional Research Service Opinion: State and Federal Authority to
Mandate COVID-19 Vaccination (Version 1) by Wen W. Shen
2021/06/12 - Texas federal judge ruled in Bridges v. Houston Methodist Hospital, 543 F.
Supp. 3d 525  (S.D. Tex. 2021), finding that informed consent doesn't apply
to  hospital  workers, because the injections are government-authorized under FDA
Emergency Use Authorization, therefore not part of experimental clinical trials or ordinary
medical treatments, therefore hospital employees cannot be legally construed as human
subjects or ordinary patients, therefore they have no individual, Constitutional liberties;
rights to privacy and against government violation of bodily integrity; or rights to be
secure in their persons against warrantless search and seizure.
2021/06/25 - FDA EUA Pfizer Fact Sheet addressing “option to accept or refuse.” This is
only one of many versions issued between December 2020 and present; it’s the one
cited by Attorney Johnsen in her legal opinion.
2021/07/06 - Dawn Johnsen, Deputy Attorney General, published DOJ Opinion: Whether
Section 564 of the Food, Drug, and Cosmetic Act Prohibits Entities from Requiring the
Use of a Vaccine Subject to an Emergency Use Authorization. Related federal
government’s position on legal status and regulatory control differences between
Emergency Use Authorization (EUA) products, Investigational New Drugs (IND) and
Investigational Device Exemptions (IDE).
2021/07/16 - Roman Catholic Pope Francis issued  Traditionis custodes, attempting to
abrogate Pope Benedict’s 2007 Summorum Pontificum, and revoke the right of Catholic
priests and faithful to celebrate the pre-1962, Traditional Latin Mass.
2021/07/29 - President Biden  directed  Department of Defense to “look into how and
when they will add COVID-19 vaccination to the list of required vaccinations for members
of the military.”
2021/08/24 - Department of Defense order from Secretary of Defense Lloyd Austin, vaxx
mandate on military personnel in Army, Navy, Air Force, Marines and Coast Guard.
2021/09 - HHS FDA Guidance: Real-World Data - Assessing Electronic Health Records
and Medical Claims Data To Support Regulatory Decision-Making for Drug and Biological
Products
2021/09/09 - President Biden signed Executive  Order  14042, vaxx mandate on federal
contractors. 86 Federal Register 50985.
2021/09/09 - President Biden signed Executive  Order  14043, vaxx mandate on federal
employees. 86 Federal Register 50989.
2021/09/09 - President Biden issued directive to Department of Labor Occupational
Safety and Health Administration (OSHA), vaxx mandate on private employers with more
than 100 employees.
2021/09/17 - President Biden signed Executive Order 14047, adding measles to the list
of quarantinable communicable diseases authorizing HHS Secretary to use force to
apprehend and detain people under  42 USC 264(b)  and  42 CFR 70.6.  86 Federal
Register 52591.
2021/11 - HHS  FDA Guidance: Real-World Data - Assessing Registries to Support
Regulatory Decision-Making for Drug and Biological Products
2021/11/05 - President Biden issued directive to Department of  Health  and Human
Services Center for Medicare and Medicaid Services (CMS), vaxx mandate
on health care workers at hospitals, nursing homes and other federally-funded facilities.
2021/11/17 - HHS Interim Final Rule - Possession, Use, and Transfer of Select Agents
and Toxins—Addition of SARS–CoV/SARS–CoV–2 Chimeric Viruses Resulting From
Any Deliberate Manipulation of SARS–CoV–2 To Incorporate Nucleic Acids Coding for
SARS–CoV Virulence Factors to the HHS List of Select Agents and Toxins. 86 Federal
Register 64075. Chimeric, lab-weaponized SARS-CoV-2 added to list of agents that
“have the potential to pose a severe threat to public  health  and safety” under 42 CFR
73.3. Attempt to block accountability by preemptively reclassifying bioweapons as legally
identical to pandemics, to block international law claims brought under the theory that
SARS-CoV-2 is a bioweapon, and not a pandemic. If classified as a bioweapon, the
Public  Health  Emergency of International Concern (international) and
public  health  emergency (federal) legal frameworks would be nullified, instead bringing
to bear federal and international laws prohibiting chemical and biological weapons.
2021/12/02 - HHS Final Rule - National Vaccine Injury Compensation Program: Adding
the Category of Vaccines Recommended for Pregnant Women to the Vaccine Injury
Table - 86 Federal Register 68423. Added vaccines recommended for pregnant women
to the list of vaccines subject to the 1986 VICP compensation scheme, so as add another
hurdle to civil suits against Covid-19 injection manufacturers, even though the products
had not yet been added to the childhood vaccine schedule that otherwise governs
access to VICP scheme. Because CDC does recommend them for pregnant women.
2021/12/27 - Congress and President Biden passed National Defense Authorization Act
FY2022 - PL 117-81, 135 Stat. 1541. At Section 716, established military vaxx tracking
system, including refusals, under 10 USC 1110 (originally re anthrax vaxx). At Section
6501, authorized US government to engage with  Bill  Gates Coalition for Epidemic
Preparedness Innovations (CEPI). More coverage.
2022/01/13 - Supreme Court ruled in Missouri v. Biden (21 A 240), Louisiana v. Biden (21
A. 241), 595 US __, (2022), asserting federal funding for hospitals and nursing homes
voids Constitutional protection for employees individual bodily integrity and informed
consent to medical treatment.
2022/02/07 -  Congressional Research Service Opinion: State and Federal Authority to
Mandate COVID-19 Vaccination
2022/02/10 - Supreme Court leaked draft opinion in Dobbs v. Jackson
Women's  Health,  leaked draft opinion  by Justice Samuel Alito. SCOTUS poised to
explicitly deny the principle of Constitutionally-protected inalienable individual rights to
personal privacy, conscience, bodily integrity, or liberty, against State exercise of
authority. Final ruling issued 06/24/2022.
2022/03/09 - President Biden signed Executive  Order  14067,  Ensuring Responsible
Development of Digital Assets, on Central Bank Digital Currencies)
2022/03/15 - Congress and President Biden passed Consolidated Appropriations Act -
PL 117-103,  136 Stat. 49. $1,274,678,000 for the Public  Health  and Social Services
Emergency Fund (HHS slush fund established in 2005). $780,000,000 for new domestic
bioweapons production, classified as ‘security countermeasures’ under the
Public Health Service Act as amended by 2004 Project Bioshield Act, 42 USC 247d-6b(c)
(1)(B); $845,000,000 to stock the Strategic National Stockpile established 1998,
controlled by the CDC within HHS 42 USC 247d-6b(a); $300,000,000 “to prepare for or
respond to an influenza pandemic,” including federally-funded construction or renovation
of privately-owned pharmaceutical manufacturing facilities, if the Secretary of Health and
Human Services finds such construction or renovation necessary; $1,000,000,000 to
establish ARPA-H: Advanced Research Program Agency -  Health, to conduct research
and development of bioweapons misbranded as public health measures; $3,880,000,000
to US Agency for International Development (US-AID) for programs mislabeled as
‘Global  Health  Programs,’ including immunization programs, HIV/AIDS programs, The
GAVI Alliance [population-control zealot  Bill  Gates’ Global Alliance for Vaccines and
Immunization] and a multilateral vaccine development partnership, for, among other
projects, “experimental contraceptive drugs, devices and medical procedures.”
2022/05/17 -  Congressional Research Service Opinion: State and Federal Authority to
Mandate COVID-19 Vaccination. (Version 9)
2022/05/17 -  Congressional Research Service Opinion: Status of Federal COVID-19
Vaccination Mandate Litigation. (Version 7)
2022/06/24 - Dobbs v. Jackson Womens Health SCOTUS decision released.
2022/07/15 - HHS Secretary Xavier Becerra extended 01/27/2020  determination that
‘public health emergency’ exists.
2022/07/22 - HHS Secretary Xavier Becerra elevated Administration for Strategic
Preparedness and Response (ASPR) from staff division to operating division, still under
HHS Assistant Secretary Dawn O'Connell.
2022/09/12 - President Biden signed Executive Order 14081 - Advancing Biotechnology
and Biomanufacturing Innovation for a Sustainable, Safe, and Secure American
Bioeconomy. 87 Federal Register 56849.
2022/09/28 - HHS-FDA Proposed Rules: Protection of Human Subjects and

Institutional Review Boards. 87 Federal Register 58733

2022/10/13 - HHS Secretary Xavier Becerra extended 01/27/2020  determination that
‘public health emergency’ exists.
2022/10/13 -  Boston  University  researchers, funded by Fauci’s NIAID, publish preprint
paper on their gain-of-function/DURC research combining the toxicity of the original
Wuhan strain of SARS-CoV-2 with the increased transmissibility of the Omicron variant to
 achieve 80% mortality in transgenic, humanized mice expressing the ACE-2
receptor.  Role of spike in the pathogenic and antigenic behavior of SARS-CoV-2 BA.1
Omicron
2022/10/18 - President Biden  National Security Memorandum (NSM-15) on Countering
Biological Threats, Enhancing Pandemic Preparedness, and Achieving Global Health
Security and National Biodefense Strategy Implementation Plan.

Summer 2022 - Pending Federal Legislation

 
 

National Defense Authorization Act  for FY2023 - Pending, HR7900. Section 6901 -
Global Health Security Act. Authorizes, creates, funds globalized military-health structure,
linking US military to global genocide apparatus operating under WHO frameworks.
Global Pandemic Prevention and Biosecurity Act - Pending,  HR3424  and  S1737. Also
included in NDAA for FY2023 at Section 6901.
2022 Covid Supplemental Appropriations Act  - Pending, HR7007. Authorizes $10.6
billion for Covid bioweapon development and deployment, including “up to
$9,850,000,000 to Biomedical Advanced Research and Development Authority [BARDA,
established 2006] for advanced research and development, manufacturing, production,
and purchase, at the discretion of the Secretary of  Health  and Human Services, of
vaccines, therapeutics, diagnostics, and supplies.”
2022 Research Investment to Spark the Economy (RISE) ACT - Pending, S.289. Senate
counterpart to Cures 2.0 Act/HR6000, Title V, Section 502. Authorizes billions in funding
for the Departments of Agriculture, Commerce, Defense, Education, Energy, the
Interior,  Health  and Human Services, and Transportation, National Aeronautics and
Space Administration (NASA), National  Science  Foundation, and Environmental
Protection Agency to provide support for research regarding COVID-19 (i.e., coronavirus
disease 2019) or research disrupted by the COVID-19 pandemic. Support may be used
to provide supplemental funding to extend the duration of a grant…that was awarded
prior to enactment, or to expand the purposes of such a grant; issue awards to research
the effects of the current pandemic and potential future pandemics; and provide flexibility
on awards to account for facility closures or other limitations during the COVID-19
public health emergency.
2022 PASTEUR Act  - Pending, HR 3932. (41 pages). Pioneering Anti-microbial
Subscriptions To End Upsurging Resistance Act. Would create subscription-based
procurement contracts between the US government and pharmaceutical corporations for
ongoing, open-ended development, purchase and deployment of drugs alleged to treat
 antibiotic-resistant infections. Appropriates $11 billion for program. Program to be
developed by committee comprised of National Institute of Allergy and Infectious
Diseases, Centers for Disease Control and Prevention, Biomedical Advanced Research
and Development Authority, Food and Drug Administration, Centers for Medicare &
Medicaid Services, Veterans Health Administration, and Department of Defense.
2022 Cures 2.0 Act  - Pending, HR6000. (173 pages.) Would legally establish Covid-
infection  injury and Covid-19 bioweapon injection injury as “long Covid,” (erasing
injection-caused injury as a separate diagnostic classification) and appropriate research
and treatment funding; would establish genomic testing program for children and teens
(corroborating evidence that government developed the bioweapons to cause listed
harms and anticipates observing those effects in the population); would establish
pharmacogenetic consulting and other programs. Title V, Section 502
is House counterpart to S.289, RISE Act (see above), to authorize billions in funding for
the Departments of Agriculture, Commerce, Defense, Education, Energy, the
Interior,  Health  and Human Services, and Transportation, National Aeronautics and
Space Administration (NASA), National  Science  Foundation, and Environmental
Protection Agency to provide support for research regarding COVID-19 (i.e., coronavirus
disease 2019) or research disrupted by the COVID-19 pandemic.

COVID-19 injectable bioweapons as case study in legalized, government-operated

domestic bioterrorism. Or: why there won’t be any civil suits, or compensatory
damages for injured victims or survivors of dead victims.

 
 
Since first realizing the implications of the many Congressional statutes and  Health  and
Human Services regulations adopted to create and operate the bioterrorism program, mostly
between 1997 and the present, I’ve been intermittently finding the specific citations for each
statement while researching related issues. 
Some statements are simply logical deductions from the first premise, corroborated by the
observable actions and inactions of Food and Drug Administration officials as the observable
injuries and deaths mount up in the American people.
Others are specifically written into the laws, but I don’t yet have the citations because I’ve
prioritized my research time investigating other issues related to the bioterrorism program.
I’m posting the information as I understand it today [June 9, 2022], despite those limitations, in
case it’s useful for readers who also follow FDA Vaccine and Related Biological Products
Advisory Committee (VRBPAC) reporting by Toby Rogers, Igor Chudov, Steve Kirsch, Jessica
Rose, and others.
They continue to rightly raise public awareness and alarm about FDA’s ongoing failure to
protect the public from the Emergency Use Authorized (EUA) products. 
But they don’t address the main reason why FDA is acting as it is.
FDA is not pulling the EUA products from the market or stopping the ‘vaccination’ campaign
because  Health  and Human Services Secretary Xavier Becerra and FDA Commissioner
Robert Califf are running the US government’s bioterrorism program jointly with Defense
Secretary Lloyd Austin, Department of Justice Attorney General Merrick Garland, Department
of Homeland Security Secretary Alejandro Majorkas, Pfizer CEO Albert Bourla, Moderna CEO
Stephane Bancel, and World  Health  Organization Director-General Tedros Adhanom
Ghebreyesus.
Main Premise
Use of EUA-covered medical countermeasure (MCM) products including masks, PCR tests,
mRNA and DNA injections, and other drugs, devices and biologics, once designated as such
by the Secretary of Health and Human Services (March 10, 2020, retroactive to February 4,
2020) “shall not be considered to constitute a clinical investigation.”  21 USC 360bbb-
3(k). FDA EUA law, adopted 1997 and amended 2003, 2004, 2005, 2013, 2017.
This is true no matter how untested, unmonitored, unsafe, or ineffective they are, no matter
whether their harmfulness to human  health  and uselessness for  infection-control are known
before use, or discovered afterward. 
Legal implications derived from the main premise:

1. There is no stopping condition.

2. EUA products are exempt from laws regulating researcher use of investigational,
experimental drugs, devices and biologics on human beings.
3. EUA products are exempt from laws regulating physician use of approved drugs, devices
and biologics as medical treatments for patients.
4. There are no manufacturers of experimental products (EUA products are not part of any
clinical investigation, and therefore not experimental.)
5. There are no government or private contracts for purchase of experimental products;
there are only contracts for ‘large scale vaccine manufacturing demonstrations.’
6. There is no act of administration of any experimental products.
7. There are no nurses or pharmacists administering experimental products.
8. There are no human subjects (of experiments) or patients (of physicians providing
treatment) receiving experimental products: no victims.
9. There is no party responsible for the wellbeing of recipients after administration of EUA
products.
10. There is no treatment group and no control group.
11. Human beings administering EUA products have no  informed consent  obligations to
provide information about ingredients, risks, benefits, alternatives, or the option to accept
 or refuse the products. See 21 USC 360bbb-3(e)(1)(A)(ii)) waiving informed consent for
unapproved products (2004); 21 USC 360bbb-3(e)(2)(A) waiving informed consent for
unapproved use of an approved product (2004); 21 USC 355(i)(4) waiving informed
consent for experimental products classified by HHS as ‘minimal risk’ drugs (2016); 21
USC 360j(g)(3)(D)(i) waiving informed consent for experimental ‘minimal risk’ devices
(2016).
12. Human beings receiving EUA products have no  informed consent  rights to receive
information about ingredients, risks, benefits, alternatives, or the option to accept or
refuse the products. See citations, bullet point above.
13. There are no Institutional Review Boards supervising administration of the experimental
products. 
14. There are no safety standards for EUA products.
15. There are no efficacy standard for EUA products. See 21 USC 360bbb-3(c)(2)(A), 1997,
2003, 2004, re: ‘may be effective.’
16. There are no clinical investigators studying the effects of EUA products on human
subjects.
17. There are no doctors, nurses, or other treatment providers providing experimental
treatment to their patients subject to the Hippocratic Oath (“first do no harm”) using EUA
products.
18. There is no coordinated, public, federal government monitoring of recipients after
receiving the products for adverse effects and deaths.
19. There is no coordinated, public, federal government data collection or analysis.
20. There is no legal requirement for medical supervision during product administration.
21. There is no legal requirement for recipient monitoring after product administration. 
22. ‘Real world evidence’ — mass administration of products to general public, followed by
collection of private/proprietary information about the effects, from  health  insurance
systems, government databases (Medicare, Medicaid, Defense Medical Epidemiology
Database, Veterans Health Administration) and other private databases — is authorized
for the purposes of FDA regulatory decisions. See 21 USC 355g. 2016.
23. There is no requirement for individual prescriptions to be written prior to dispensing EUA
products, and products dispensed without prescriptions “shall not be deemed adulterated
or misbranded.” See 21 USC 360bbb-3a(d). 2013.
24. Manufacturers, as contractors, are considered HHS employees for purposes of legal
immunity under Federal Tort Claims Act. See 42 USC 247d-6a(d)(2)(A).
25. DOD is authorized to contract with pharmaceutical corporations to conduct ‘prototype’
experiments on the general public, and under such contracts, is exempt from legal
obligation to comply with Good Clinical Practices or other FDA regulations. See 10 USC
2371b (2015), renumbered 10 USC 4022 (Jan. 1, 2021, effective Jan. 1, 2022)
26. One of the factors to be considered by HHS secretary in making determinations about
EUA products (qualified security countermeasures) and use of Special Reserve
Fund/Strategic National Stockpile appropriations to procure them is "whether there is a
lack of a significant commercial market for the product at the time of procurement, other
than as a security countermeasure." See 42 USC 247d-6b (c)(5)(B)(iii)
27. There are no required standards for quality-control in manufacturing; no inspections of
manufacturing procedures; no prohibition on wide variability among lots; no prohibition on
adulteration; and no required compliance with Current Good Manufacturing Practices.
EUA products, even though unregulated and non-standardized, “shall not be deemed
adulterated or misbranded.” See 21 USC 360bbb-3a(c). 2013.
28. There are no labeling requirements regarding the contents or ingredients in EUA
products. 21 USC 360bbb-3(e)(2)(B)(ii). 2004.
29. There is no limitation of administration of EUA products past their expiration dates.
30. There cannot be clinical trial fraud, because there are no clinical investigations, no
investigational drugs, no investigators and no human subjects.
31. There are no marketing standards.
32. There cannot be consumer fraud, because the only legal parties to the financial
transactions are the US government (DOD) as buyer; the US government (HHS) as
regulator authorizing exemptions from consumer protection laws that otherwise apply to
medical products; and the pharmaceutical corporations as sellers, contracted to develop
and manufacture the products. There are no commercial pharmaceutical products, no
commercial marketplace, and no commercial market consumers.
33. There is no access to courts for judicial review of the facts or law relating to HHS
Secretary declarations of EUA products, which are committed to agency
discretion. See 42 USC 247d-6d(b)(7). 2005.
34. There is no access for plaintiffs, to civil courts for judicial review, and no entity to whom
civil liability can attach, for injuries and deaths caused by declared covered
countermeasures, unless and until FDA/HHS and/or Attorney General/DOJ file
enforcement action against manufacturers and prove willful misconduct proximate to
injury or death, but HHS and DOJ have operated the EUA product program together with
the manufacturers since inception, and will not prosecute their co-conspirators.  See  42
USC 247d-6d. 2005.
35. Even if there were access to courts for judicial review, and a fact-finder found evidence of
harms caused by administration of products to recipients, and even evidence that those
who caused the harms, by developing, manufacturing, distributing and/or administering
the EUA products, knew the EUA products were toxic and knew their own actions were
harmful, “just following orders” is an authorized, legal defense. See 42 USC 247d-6d(c)
(4). 2005.
Summary:
There are no actions that can be legally classified as crimes or civil torts; there are no medical
battery or homicide victims, or plaintiffs; and there are no medical batterers or murderers.
Because legally, nothing has been done, and no one has done anything, to anyone else.
The recursive loop can be infinite, as covered countermeasures are developed, authorized
and deployed, through HHS Secretary EUA declarations, as treatments for complications from
prior countermeasures.
 
https://bailiwicknews.substack.com/p/american-domestic-bioterrorism-program