IPR Notes, UNIT-1
IPR Notes, UNIT-1
Intellectual property rights are the legal rights that cover the privileges given to individuals
who are the owners and inventors of a work, and have created something with their intellectual
creativity. Individuals related to areas such as literature, music, invention, etc., can be granted
such rights, which can then be used in the business practices by them.
The creator/inventor gets exclusive rights against any misuse or use of work without his/her
prior information. However, the rights are granted for a limited period of time to maintain
equilibrium.
Intellectual Property
Intellectual property is an intangible creation of the human mind, usually expressed or
translated into a tangible form that is assigned certain rights of property. Examples of
intellectual property include an author's copyright on a book or article, a distinctive logo design
representing a soft drink company and its products, unique design elements of a web site, or a
patent on the process to manufacture chewing gum.
Intellectual Property Rights
Intellectual property rights (IPR) can be defined as the rights given to people over the creation
of their minds. They usually give the creator an exclusive right over the use of his/her creations
for a certain period of time. Intellectual property (IP) refers to creations of the mind: inventions,
literary and artistic works, and symbols, names, images, and designs used in commerce.
IPR in Agriculture
Scientific advances in plant breeding led to the “Green Revolution”, regarded as one of the
most important achievements to feed the world during the last century. Mostly staple cereal
crops, particularly wheat, rice and maize, were targeted by the “Green Revolution”. Towards
the end of the 20th century 370 kg of cereals per person were harvested versus to only 275 kg
in the mid-20th century (i.e., in excess of 33% per capita gain). In other crops the gains since
the early 1960s were about 20%. In simple language, this has helped alleviate starvation and
malnutrition in almost 1 billion people. However, the “Green Revolution” approach appears to
have been exploited close to its limits, and other alternative approaches are required to continue
improving plants and livestock for the agriculture of the 21st century. This will be very
important considering that about 12% of the world’s land surface grows crops and that the per
capita area to support food production will decline from 0.44 ha in 1961 to 0.15 in 2050.
Biotechnology offers today new and better means to complement classical breeding tools for
the genetic improvement of both crops and livestock. Biotechnology offers new means for
achieving a higher intensity of selection, e.g. through in vitro techniques, or for a more
objective selection of individuals through genetic markers. Likewise, genetically engineered
(so-called transgenic or GMO) plants offer new methods for inserting new genes to the
breeding pool, thus enhancing the quality of the new variety. Let us go on to discuss some
examples of the new biotechnology and indicate some of the value these new products may
have for the developing world.
Key Applications
The most common and successful applications of biotechnology for crop and livestock
improvements include:
Cell and Tissue Culture. This is the growing of plant cells as a way of producing
uniform individuals or for shortening the number of years needed to produce and release
new varieties. Tissue culture techniques have led to dramatic production increases in
cassava, yams, bananas and plantains, palms, and potato to mention only a few.
Genetic Engineering for pest and disease resistance. There are now hundreds of
millions of acres of genetically engineered crops grown in North America and
Argentina and increasing interest is being shown in these in some developing countries,
particularly China.
DNA fingerprinting, the same as used in forensic science, is used to gain better insight
into pathogen diversity that may allow pre-empting breakdowns of host plant resistance
to pests and diseases.
Better management of seed storage facilities, so-called gene banks, and greater
knowledge of biodiversity can be achieved with the aid of molecular-aided analyses.
The more we know about this genetic diversity, the more we can apply it to produce
higher yielding, more resistant materials.
Finding the location of genes on a chromosome with DNA markers will allow scientists
to custom make plants and animals with specific disease and pest tolerance.
New tools to test for pests, diseases and to detect dangerous food contaminants. These
techniques will help us produce not only more food, [but food that is nutritious and safe
to eat since it may contain lower levels of toxins and/or pesticides]
The identification, isolation and cloning of new genes controlling specific characteristics will
also facilitate the development of a more stable, diversified germplasm with improved
resistance to diseases and pests, stress tolerance, better food quality, and higher productivity.
For example genes allowing a reduced crop cycle or modified plant structure will provide
pathways for new cropping systems.
Nonetheless, conventional crossbreeding will be still required for an appropriate testing and
further transfer of these genes to the advanced breeding pools of the crop. Furthermore, seed
delivery systems of improved genotypes should be in place to promote the utilization of new
cultivars, which will enhance and stabilize the agricultural production, farm income, and farm-
family welfare. In brief, the new tools of biotechnology alone cannot provide the answer to
genetic improvement, but they are facilitating and accelerating the pace in the development of
new cultivars.
Some of the current achievements of biotechnology applications for improving agriculture are
surpassing the original expectations and the outlook appears to be even more promising.
However, the fulfillment and impact of biotechnology does not depend only in the
demonstrated research advances and technology ensuing from their applications but on both
favorable regulatory frameworks by national governments (or through regional agreements)
and positive public acceptance.
The office of the Controller General of Patents, Designs and trademarks (CGPDTM), a
subordinate Office under The Department for Promotion of Industry and Internal Trade
(DPIIT), carries out statutory functions related to grant of Patents and registration of
Trademarks, Designs and Geographical Indications. The registration of copyrights is
administered by the Registrar of Copyright Office, working under the CGPDTM. It functions
out of offices situated in Delhi, Kolkata, Mumbai, Chennai and Ahmadabad, while the Central
IP Training Academy is at Nagpur.
The appropriate office of the patent office shall be the head office of the patent office or the
branch office as the case may be within whose territorial limits. Residence of applicant or
Domicile; or their place of business; or the place where the invention actually originated.
The CGPDTM supervises the functioning of the following IP offices:
i. The Patent Office’s (including the Design Wing) at Chennai, Delhi, Kolkata & Mumbai.
ii. The Patent Information System (PIS) and Rajiv Gandhi National Institute of Intellectual
Property Management (RGNIIPM) at Nagpur.
iii. The Trade marks Registry at Ahmadabad, Chennai, Delhi, Kolkata & Mumbai.
iv. The Geographical Indications Registry (GIR) at Chennai.
v. The Copyright Office at Delhi.
vi. The Semiconductor Integrated Circuits Layout-Design Registry at Delhi.
Office Territorial Jurisdiction
Patent Office Branch, Chennai The States of Telangana, Andhra Pradesh,
Karnataka, Kerala, Tamil Nadu and the Union
Territories of Pondicherry and Lakshadweep
Patent Office Branch, Mumbai The States of Maharashtra, Gujarat, Madhya
Pradesh, Goa and Chhattisgarh and the Union
Territories of Daman and Diu & Dadra
and Nagar Haveli.
Patent Office Branch, New Delhi The States of Haryana, Himachal Pradesh,
Jammu and Kashmir, Punjab, Rajasthan, Uttar
Pradesh, Uttaranchal, Delhi and the Union
Territory of Chandigarh.
Patent Office, Kolkata The rest of India
There are a number of International organizations and agencies that promote the use and
protection
of intellectual property. Although these organizations are discussed in more detail in the
chapters to
follow, a brief introduction may be helpful:
International Trademark Association (INTA) is a not-for-profit international association
composed chiefly of trademark owners and practitioners. It is a global association. Trademark
owners and professionals dedicated in supporting trademarks and related IP in order to protect
consumers and to promote fair and effective commerce. More than 4000 (Present 6500
member) companies and law firms more than 150 (Present 190 countries) countries belong to
INTA, together with others interested in promoting trademarks. INTA offers a wide variety of
educational seminars and publications, including many worthwhile materials available at no
cost on the Internet (see INTA’s home page at http://www.inta.org). INTA members have
collectively contributes almost US $ 12 trillion to global GDP annually. INTA undertakes
advocacy [active support] work throughout the world to advance trademarks and offers
educational programs and informational and legal resources of global interest. Its head quarter
in New York City, INTA also has offices in Brussels, Shanghai and Washington DC and
representative in Geneva and Mumbai. This association was founded in 1878 by 17 merchants
and manufacturers who saw a need for an organization. The INTA is formed to protect and
promote the rights of trademark owners, to secure useful legislation (the process of making
laws), and to give aid and encouragement to all efforts for the advancement and observance of
trademark rights.
Berne Convention for the Protection of Literary and Artistic Works (the Berne
Convention) An International copyright treaty called the convention for the protection of
Literary and Artistic works signed at Berne, Switzerland in 1886 under the leadership of Victor
Hugo to protect literary and artistic works. It has more than 145 member nations. The United
States became a party to the Berne Convention in 1989. The Berne Convention is administered
by WIPO and is based on the precept that each member nation must treat nation must treat
nationals of other member countries like its own nationals for purposes of copyright (the
principle of “nation treatment”). In addition to establishing a system of equal treatment that
internationalized copyright amongst signatories, the agreement also required member states
to provide strong minimum standards for copyrights law. It was influenced by the French “right
of the author”.
Madrid Protocol It is a legal basis is the multilateral treaties Madrid (it is a city situated in
Spain) Agreement concerning the International Registration of Marks of 1891, as well as the
protocol relating to the Madrid Agreement 1989. The Madrid system provides a centrally
administered system of obtaining a bundle of trademark registration in separate jurisdiction.
The protocol is a filing treaties and not substantive harmonization treaty. It provides a cost-
effective and efficient way for trademark holder. It came into existence in 1996. It allows
trademark protection for more than sixty countries, including all 25 countries of the European
Union.
Paris Convention The Paris convention for the protection of Industrial Property, signed in
Paris, France, on 20th March 1883, was one of the first Intellectual Property treaties, after a
diplomatic conference in Paris, France, on 20 March 1883 by Eleven (11) countries. According
to Articles 2 and 3 of this treaty, juristic (one who has through knowledge and experience of
law) and natural persons who are either national of or domiciled in a state party to the
convention. The convention is currently still force. The substantive provisions of the
convention fall into three main categories: National Treatment, Priority right and Common
Rules.
An applicant for a trademark has six months after filing an application in any of the more than
160 member nations to file a corresponding application in any of the other member countries
of the Paris Convention and obtain the benefits of the first filing date. Similar priority is
afforded for utility patent applications, although the priority period is one year rather than six
months. The Paris Convention is administered by WIPO.
North American Free Trade Agreement (NAFTA) came into effect on January 1, 1994, and
is adhered to by the United States, Canada, and Mexico. The NAFTA resulted in some changes
to U.S. trademark law, primarily with regard to marks that include geographical terms. The
NAFTA was built on the success of the Canada-U.S Free Trade Agreement and provided a
compliment to Canada’s efforts through the WTO agreements by making deeper commitments
in some key areas. This agreement has brought economic growth and rising standards of living
for people in all three countries. General Agreement on Tariffs and Trade (GATT) was
concluded in 1994 and is adhered to by most of the major industrialized nations in the world.
The most significant changes to U.S intellectual property law from GATT are that nonuse of a
trademark for three years creates a presumption the mark has Smartzworld.com
Smartworld.asia jntuworldupdates.org Specworld.in been abandoned and that the duration of
utility patent is now twenty years from the filing date of the application (rather than seventeen
years from the date the patent issued, as was previously the case).
Are there any restrictions in filing outside India for Indian residents?
Yes, the following provisions have to be complied with, in case of foreign filings by Indian
Residents:
– If an application is filed in India, then there is a mandatory waiting period for at least 6 weeks
before filing outside India, else a request for a foreign filing permit at the patent office must be
submitted, and only after getting the permit, one can do the filing outside India.
– If the applicant wants to file directly outside India, without filing in India first, then again, a
request for a foreign filing permit at the patent office must be submitted, and only after getting
the permit, one can do the filing outside India.
Failure to take permission from IPO before the filing of foreign application can lead to the
abandonment of the Indian Patent application and if granted, then revocation of the patent. One
might even face imprisonment up to 2 years or a fine or both.
1. Standards: It sets minimum protection rules for different types of IP, based on
existing conventions (Paris and Berne). Countries can go beyond these standards but
must at least meet the minimum.
2. Enforcement: It outlines procedures to help people enforce their IP rights, like court
actions and remedies.
3. Dispute Settlement: Disagreements between countries about IP are handled by the
World Trade Organization (WTO).
The agreement also ensures equal treatment between members and allows developing
countries more time to adapt. Countries can create stricter protections if they wish and can
choose how to apply the rules within their legal systems.
It also emphasizes fair access to IP and technology for all, while allowing some exceptions
for public health and other important reasons. For example, developing nations have some
flexibility in providing patent protection for pharmaceuticals.
Patents
The TRIPS Agreement requires Member countries to make patents available for any
inventions, whether products or processes, in all fields of technology without discrimination,
subject to the normal tests of novelty, inventiveness and industrial applicability. It is also
required that patents be available and patent rights enjoyable without discrimination as to the
place of invention and whether products are imported or locally produced (Article 27.1).
There are three permissible exceptions to the basic rule on patentability. One is for inventions
contrary to ordre public or morality; this explicitly includes inventions dangerous to human,
animal or plant life or health or seriously prejudicial to the environment. The use of this
exception is subject to the condition that the commercial exploitation of the invention must
also be prevented and this prevention must be necessary for the protection of ordre public or
morality (Article 27.2).
The second exception is that Members may exclude from patentability diagnostic, therapeutic
and surgical methods for the treatment of humans or animals (Article 27.3(a)).
The third is that Members may exclude plants and animals other than micro-organisms and
essentially biological processes for the production of plants or animals other than non-
biological and microbiological processes. However, any country excluding plant varieties from
patent protection must provide an effective sui generis system of protection. Moreover, the
whole provision is subject to review four years after entry into force of the Agreement
(Article 27.3(b)).
The exclusive rights that must be conferred by a product patent are the ones of making, using,
offering for sale, selling, and importing for these purposes. Process patent protection must give
rights not only over use of the process but also over products obtained directly by the process.
Patent owners shall also have the right to assign, or transfer by succession, the patent and to
conclude licensing contracts (Article 28).
Members may provide limited exceptions to the exclusive rights conferred by a patent,
provided that such exceptions do not unreasonably conflict with a normal exploitation of the
patent and do not unreasonably prejudice the legitimate interests of the patent owner, taking
account of the legitimate interests of third parties (Article 30).
The term of protection available shall not end before the expiration of a period of 20 years
counted from the filing date (Article 33).
Members shall require that an applicant for a patent shall disclose the invention in a manner
sufficiently clear and complete for the invention to be carried out by a person skilled in the art
and may require the applicant to indicate the best mode for carrying out the invention known
to the inventor at the filing date or, where priority is claimed, at the priority date of the
application (Article 29.1).
If the subject-matter of a patent is a process for obtaining a product, the judicial authorities
shall have the authority to order the defendant to prove that the process to obtain an identical
product is different from the patented process, where certain conditions indicating a likelihood
that the protected process was used are met (Article 34).
Compulsory licensing and government use without the authorization of the right holder are
allowed, but are made subject to conditions aimed at protecting the legitimate interests of the
right holder. The conditions are mainly contained in Article 31. These include the obligation,
as a general rule, to grant such licences only if an unsuccessful attempt has been made to
acquire a voluntary licence on reasonable terms and conditions within a reasonable period of
time; the requirement to pay adequate remuneration in the circumstances of each case, taking
into account the economic value of the licence; and a requirement that decisions be subject to
judicial or other independent review by a distinct higher authority. Certain of these conditions
are relaxed where compulsory licences are employed to remedy practices that have been
established as anticompetitive by a legal process. These conditions should be read together
with the related provisions of Article 27.1, which require that patent rights shall be enjoyable
without discrimination as to the field of technology, and whether products are imported or
locally produced.
Layout-designs of integrated circuits
Article 35 of the TRIPS Agreement requires Member countries to protect the layout-designs of
integrated circuits in accordance with the provisions of the IPIC Treaty (the Treaty on
Intellectual Property in Respect of Integrated Circuits), negotiated under the auspices of WIPO
in 1989. These provisions deal with, inter alia, the definitions of “integrated circuit” and
“layout-design (topography)”, requirements for protection, exclusive rights, and limitations, as
well as exploitation, registration and disclosure. An “integrated circuit” means a product, in its
final form or an intermediate form, in which the elements, at least one of which is an active
element, and some or all of the interconnections are integrally formed in and/or on a piece of
material and which is intended to perform an electronic function. A “layout-design
(topography)” is defined as the three-dimensional disposition, however expressed, of the
elements, at least one of which is an active element, and of some or all of the interconnections
of an integrated circuit, or such a three-dimensional disposition prepared for an integrated
circuit intended for manufacture. The obligation to protect layout-designs applies to such
layout-designs that are original in the sense that they are the result of their creators' own
intellectual effort and are not commonplace among creators of layout-designs and
manufacturers of integrated circuits at the time of their creation. The exclusive rights include
the right of reproduction and the right of importation, sale and other distribution for commercial
purposes. Certain limitations to these rights are provided for.
In addition to requiring Member countries to protect the layout-designs of integrated circuits
in accordance with the provisions of the IPIC Treaty, the TRIPS Agreement clarifies and/or
builds on four points. These points relate to the term of protection (ten years instead of eight,
Article 38), the applicability of the protection to articles containing infringing integrated
circuits (last sub clause of Article 36) and the treatment of innocent infringers (Article 37.1).
The conditions in Article 31 of the TRIPS Agreement apply mutatis mutandis to compulsory
or non-voluntary licensing of a layout-design or to its use by or for the government without the
authorization of the right holder, instead of the provisions of the IPIC Treaty on compulsory
licensing (Article 37.2).
Protection of undisclosed information
The TRIPS Agreement requires undisclosed information -- trade secrets or know-how -- to
benefit from protection. According to Article 39.2, the protection must apply to information
that is secret, that has commercial value because it is secret and that has been subject to
reasonable steps to keep it secret. The Agreement does not require undisclosed information to
be treated as a form of property, but it does require that a person lawfully in control of such
information must have the possibility of preventing it from being disclosed to, acquired by, or
used by others without his or her consent in a manner contrary to honest commercial practices.
“Manner contrary to honest commercial practices” includes breach of contract, breach of
confidence and inducement to breach, as well as the acquisition of undisclosed information by
third parties who knew, or were grossly negligent in failing to know, that such practices were
involved in the acquisition.
The Agreement also contains provisions on undisclosed test data and other data whose
submission is required by governments as a condition of approving the marketing of
pharmaceutical or agricultural chemical products which use new chemical entities. In such a
situation the Member government concerned must protect the data against unfair commercial
use. In addition, Members must protect such data against disclosure, except where necessary
to protect the public, or unless steps are taken to ensure that the data are protected against unfair
commercial use.
Control of anti-competitive practices in contractual licence
Article 40 of the TRIPS Agreement recognizes that some licensing practices or conditions
pertaining to intellectual property rights which restrain competition may have adverse effects
on trade and may impede the transfer and dissemination of technology (paragraph 1). Member
countries may adopt, consistently with the other provisions of the Agreement, appropriate
measures to prevent or control practices in the licensing of intellectual property rights which
are abusive and anti-competitive (paragraph 2). The Agreement provides for a mechanism
whereby a country seeking to take action against such practices involving the companies of
another Member country can enter into consultations with that other Member and exchange
publicly available non-confidential information of relevance to the matter in question and of
other information available to that Member, subject to domestic law and to the conclusion of
mutually satisfactory agreements concerning the safeguarding of its confidentiality by the
requesting Member (paragraph 3). Similarly, a country whose companies are subject to such
action in another Member can enter into consultations with that Member (paragraph 4).
Patent Registration grants intellectual property rights to the inventor of a new product,
technology, or process. These rights give the inventor an exclusive opportunity to sell,
manufacture, and import the invented product for 20 years from the application date if it gets
approved. Let’s understand how you can get registration of a patent and what are the crucial
steps involved in the procedure for obtaining a patent that you need to take.
Patent Registration process or procedure for obtaining patent begins with the crucial step of
patent search where you analyse the novelty aspect of your invention. Only if your invention
is novel, innovative, and state-of-the-art, you can proceed with the patent filing procedure for
obtaining patent further. The Patent Act 1970 gives you the flexibility of filing a provisional
patent application if your invention is in the development stage and replacing it with the
complete application as soon as the product is developed or within 1 year from the filing date.
For completely developed products, you can directly file the complete application with a
detailed specification.
What is Patent Registration?
Patent Registration is a legal process of securing exclusive rights over a newly invented
product. These include the rights to manufacture, sell, and import the product for the next 20
years since the patent application filing date. It helps an inventor capitalize on his intellectual
property and reward his innovative ideas, research, and development efforts appropriately.
Wondering about its legal framework? Patent Registration is governed under the Indian Patent
Act of 1970 and administered by the office of the Controller General of Patents.
Eligibility for Registration Process of Patent in India
Inventors can secure patents only if they are completely novel. This means that a similar or
identical invention has never been introduced in the public domain before. Simply put, the new
invention should be absolutely state-of-the-art. The novelty criteria need to be met before the
patent application is actually filed. Also, the invention should have an innovative function or
feature that’s not obviously known to the public. Besides novelty, another important
requirement is Industrial Application. The invented product must have a practical utility and
be capable of being manufactured in the industry. This directly excludes any new object that’s
solely made for aesthetic purposes. Even if these criteria are met, an invented product cannot
be patented if it is prohibited under Sections 3 and 4 of the Patents Act.
Patent Registration Criteria
1. Novelty: New & Innovative; Publicly Disclosed for the first time.
2. Inventive Step: Far from public knowledge; state-of-the-art technical advancements
3. Industrial Applicability: A practical utility and capability of being manufactured in
an industrial setup.
4. Not Prohibited under Sections 3 & 4 of the Patent Act: Must be legally eligible to
be patented.
Types of Patent Application
Based on the terms of patent protection, there are two types of patent applications. Firstly, we
have the Provisional Application to be filed for a temporary protection of 1 year while the
product is in the development stage. This allows time to develop the product without the fear
of losing exclusive rights over it. Secondly, we have the complete application which is filed
for full-term patent protection. It can be filed directly or in the replacement of the provisional
patent, once it lapses.
Besides, based on purpose, we can classify patent applications into 6 types. Let’s see what they
are:
Ordinary Patent Application: For patent protection within India.
PCT National Phase Patent Application: Allows the applicant to enter the PCT
process and get patent protection internationally.
PCT International Patent Application: Final stage of PCT process, international
application for patent registration.
Convention Patent Application: Used to claim priority based on an earlier application
filed in a convention country.
Divisional Patent Application: Used to divide an existing patent application into
multiple separate applications to secure multiple inventions.
Patent of Addition Application: Used to apply for an improvement or modification
of an already existing and patented invention.
How to Apply for Patent in India?: Patent Filing Process in India
The procedure for obtaining patent involves a series of simple steps. You will first have to
select the appropriate application to file. Then, visit the IP India portal and begin the application
process. Remember, documents are the most crucial aspect of your application and will decide
its success.