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© Copyright 2013. AssignmentLab.com. All rights reserved. Personnel Selection. The process of
gathering & assessing information about job candidates & ultimately making personnel decisions.
Environmental Factors. Legal considerations Time constraints Organizational hierarchy Hiring
policies Applicant pool Type of organization Other HR functions. Laboratory Personnel. Dr/Ehsan
Moahmen Rizk. Organization. Personnel. Equipment. Purchasing & Inventory. Information
Management. Documents & Records. Occurrence Management. Process Improvement. Customer
Service. Facilities & Safety. The Quality Management System. Performance Appraisal competencies
professionalbehavior adherence to policy observation to safety communication customer service
Efficiency Personnel-Module 12 27 An excellent introduction must be used to inform readers what
your report is all about. But there is a procedure on how to do it. It should be in personal words and
ensure you give a clear synopsis. Write down what you were trying to clarify or find using the
experiment, your procedures, the main principles you followed, and finally the findings. Typically, it
is like a short paraphrasing of your report and should never be written in the first person. An Image
/Link below is provided (as is) to download presentation Post this Lab Assistant job to over 200 job
boards at once. 2.2 Terms used in parasitology, The Laboratory Support Staff is part of the
Laboratory Support and External Laboratory Oversite Branch under the direction of the Branch
Manager. േകരള ിെല എ ാ HIGHER SECONDARY LAB ASSISTANTS-നും
പേയാജന പദമായി െവബ്ൈസ ് നവീകരി ു ു . Laboratory director • provide
advice to those requesting information about the choice of tests, the use of the laboratory service and
the interpretation of laboratory data • relate and function effectively with: • applicable accrediting
and regulatory agencies, • Clinical Staff • the healthcare community • the patient population served
Personnel-Module 12 The task of managing the operations of an organization is not a piece of cake.
We offer the best HR assignment help with a team of over 1000+ PhD proficients available to assist
you with topics such as Equal Employment Opportunity, Job analysis, Strategic HR management,
Recruiting and labour Markets, Cross cultural management and so on. Download presentation by
click this link. While downloading, if for some reason you are not able to download a presentation,
the publisher may have deleted the file from their server. Laboratory Personnel. Dr/Ehsan Moahmen
Rizk. Organization. Personnel. Equipment. Purchasing & Inventory. Information Management.
Documents & Records. Occurrence Management. Process Improvement. Customer Service. Facilities
& Safety. The Quality Management System. On analysis, raw data is presented as it was found. The
figures should be recorded down as they appeared without addition or subtraction. Always ensure
this raw data is entirely factual. Data should be recorded as it was seen for analysis purposes. A)
Haemophilus influenzae 1.10 Culture media-General introduction to different types of culture media.
0% Operations Management is chiefly concerned with planning, supervising production,
manufacturing of goods & services and Logistics management. Experts in Operation Management
assignment help should possess great understanding of different tools including use of Microsoft
Project software and various logistics management tools. A study on logistics and operations
management requires deep concentration and the ability to look at complex situations, breaking it
down to small events or phases and solving the assignment. Click here Biological/pharmaceutical
manufacturing equipment Assignment help can only be excellent when it is high-quality, plagiarism-
free work, which can only be achieved using high-quality in-house writers. Hence to categorically
serve the purpose of client satisfaction as the primary motive, regular training and quality control is
our priority. Each customer is treated at the same level, and to ensure the same, we do not even
accept any additional payment if offered by any client. Is the category for this document correct?
The Laboratory Support Staff is responsible for scheduling, receiving and tracking all samples
through the Region 6 Laboratory Services and Applied Science Division (LSASD). D) Only drugs
can be eaten in the laboratory Internal audits (continue) • Audits should be formally planned,
organized and carried out by the quality manager or designated qualified personnel. The procedures
for internal audits should be defined and documented and include the types of audit, frequencies,
methodologies and required documentation. • The results of internal audits should be submitted to
laboratory management for review. Personnel-Module 12 To contact NDG technical support from the
Help tool, click the Leave us a message button under the suggestions. Laboratory Manger •
Responsible for the day-to-day management of the testing laboratory • Ensuring that there are
enough personnel with adequate training and experience to conduct the work • Ensuring that the
laboratory has a manual of standard operating procedures that are complete, up-to-date, available for
personnel performing tests, and followed by those personnel Personnel-Module 12
1.Circular No 01/10711/HSE/94/G.Edn dtd 27.09.1995. Did you find mistakes in interface or texts?
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us! Download Policy: Content on the Website is provided to you AS IS for your information and
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supply some information about the problem you are experiencing and what course or lab set you
experienced the issues with. If you are able, please take a screenshot of the issue or error you are
experiencing. C) Nothing can be eaten, drunk, or taken in the laboratory 4.1 Perform VDRL and
HIV tests. 4. In Botany/Zoology labs,the microscopes,slides,cover slips etc: should be cleaned
properly after every practical.they should be cleaned properly after every practical.They should also
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and proper disposal of unwanted materials. If you are able, please take a screenshot of the issue you
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Internal audits (continue) • Audits should be formally planned, organized and carried out by the
quality manager or designated qualified personnel. The procedures for internal audits should be
defined and documented and include the types of audit, frequencies, methodologies and required
documentation. • The results of internal audits should be submitted to laboratory management for
review. Personnel-Module 12 Ans. It assesses the individual’s organizational and administrative
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Quinney 1. Duty time of Lab attenders is 9.15 am to 4.30 pm with an interval of 45minutes for
lunch.They should keep the lab open during these hours and should be present in the Laboratory
concerned.
D)
Toga
virus
Pathology
is
all
about
the
extensive
study
of
diseases,
and
the
pathologists
monitor
laboratory
testing
and
figure
out
different
cytological
specimens.
Moreover,
the
field
of
laboratory
medicine
is
categorized
into
two
parts:
clinical
pathology
and
anatomic
pathology.
Clinical
pathology
is
all
about
testing
the
blood
and
urine
of
patients
and
features
key
areas
like
clinical
chemistry,
microbiology,
and
immunohematology.
On
the
other
hand,
anatomic
pathology
is
all
about
testing
tissue
specimens
and
the
examinations
of
tendons,
ligaments,
and
muscles
using
a
microscope.
The
anatomic
pathology
relates
to
metabolic,
traumatic
and
neoplastic
diseases
of
bones
and
joints.
Seek
our
laboratory
medicine
assignment
help
to
you
explore
more
about
the
field
and
include
that
crucial
information
in
your
assignments.
02:00
PM
biological
scientist
iv
-
ses
-
Department
of
Management
Services
©
2013
-
2024
studylib.net
all
other
trademarks
and
copyrights
are
the
property
of
their
respective
owners
1.
Spring
Semester
2011-
12
University
of
Puerto
Rico
-
Cayey
RISE
Program
Instructions
for
Laboratory
Writing
Assignments
1.
For
each
assignment
you
should
write
a
summaryparagraph
of
8-
10
sentences
and
a
range
from
160
-
170
words.
2.
A
template
for
each
assignment
is
attached.
Once
you
complete
the
template
email
it
to
Dr.
Elena
Gonzalez;
she
will
grade
it
using
the
rubric
below
and
return
it
to
you.
Within
the
next
two
days,
you
will
email
it
to
me
with
the
corrections
incorporated.
In
your
summary
include
a
reference
to
each
one
of
the
criteria
in
the
rubric
below.
3.
Email
subject
should
include:
Your
register
number;
first
name;
Assignment
#
and
hand-
in
date.
Example:
1.
Osvaldo
Assignment
2
March
__
Rubric
for
Assessing
Laboratory
Summaries
Name
Grade
Date
Points
Assignment
Number
30
Points
Total
A.
PURPOSE
LAB
TECHNIQUE
1
2
3
4
5
Refers
to
purpose
and
objectives
of
the
lab
techniques
B.
BIOLOGICAL
COMPETENCE
Demonstrates
knowledge
oflaboratory
procedures
Reports
findings
adequately
C.
ENGLISH
COMPETENCE
Uses
correct
grammar,
*
syntax,spelling,
and
punctuation
Demonstrates
clarity
and
coherence
D.
CRITICAL
THINKING
Identifies
applications
and
or
implications
of
the
study
in
concluding
29/
30
Excellent
work!University
of
Puerto
Rico
-
Cayey
david
bruce
centre
for
american
studies
A
career
for
the
lab
assistant
offers
improvement
chances
with
better
enduring
care
without
having
any
actual
interactions
with
the
patients.
You
can
also
pursue
your
career
as
a
freelancer,
which
will
also
promise
great
and
increased
earnings.
The
Role
of
Medical
Laboratory
Assistants
Assignment.
Retrieved
from
https:/
/
studentshare.org/
health-
sciences-
medicine/
1746524-
the-
role-
of-
medical-
laboratory-
assistants
The
Role
of
Medical
Laboratory
Assistants:
In
the
recent
era
of
medical
field,
the
diagnostics
largely
depend
on
clinical,
radiological
and
laboratory
findings,
so
the
role
of
pathologists
as
well
as
lab
assistants
is
of
utmost
importance
as
any
ignorance
or
lack
of
latest
knowledge
on
their
part
can
be
detrimental
to
the
patient.
Medical
Laboratory
Assistants
(MLAs)
are
mainly
involved
in
the
preparation
as
well
as
in
some
cases
the
processing
of
the
patient
samples.
They
are
also
required
to
perform
some
pre
requisite
tests
which
are
required
to
aid
the
pathologist
or
hematologist
in
performing
the
final
analysis.
But
the
main
duty
of
MLAs
is
to
process
the
sample
so
the
MLA
should
have
a
sound
knowledge
about
the
sampling
and
the
processing
techniques
as
well
as
the
local
recommendations
of
the
regional
medical
legislative
authority.
Now
in
order
to
have
an
overview
of
the
work
of
MLAs
we’ll
try
to
answer
a
questionnaire
to
highlights
their
duties
as
well
as
its
impact
in
the
medical
field.
1.
What
are
the
principles
of
testing
planning
techniques?
The
main
principles
of
planning
a
test
include
the
propose
of
carrying
out
the
test,
the
knowledge
of
the
clinical
suspicion
for
a
particular
disease.
Then
the
time
frame
of
performance
is
planned
followed
by
the
list
of
the
equipment
and
the
chemical
used
and
then
the
standard
procedures
for
the
investigation
are
gone
through
in
detail
to
exclude
the
possibility
of
missing
anything.
2.
What
methods
can
be
used
for
controlling
test
variables?
Basically
the
responsibility
of
accurate
and
timely
reporting
of
test
results
lies
on
the
personnel
working
in
the
laboratory
as
there
are
many
problems
which
can
arise
even
before
the
sample
has
undergone
the
analytical
process.
These
errors
can
only
be
tackled
properly
if
prior
understanding
of
the
process
as
well
as
the
capability
to
identify
any
error
in
these
processes
is
present
in
the
MLAs.
In
addition
to
this,
controlled
and
correct
interpretation
of
results
needs
comprehensive
knowledge
of
analytical,
biological
and
pathophysiological
variability
and
the
extent
of
this
change.
There
should
also
be
sound
knowledge
about
the
time
span
in
which
changes
can
occur
in
the
sample
resulting
in
the
variations
and
errors
in
the
final
results.
3.
What
are
concepts
of
repeatability
and
reproducibility?
Reproducibility
is
one
of
the
main
aspects
of
the
laboratory
working,
and
refers
to
the
ability
of
a
test
or
experiment
to
be
accurately
reproduced,
by
someone
else
working
independently.
Repeatability
is
different
from
reproducibility
as
it
measures
the
rate
of
success
in
different
experiments
conducted
by
the
same
group
of
experimenters.
Reproducibility
shows
the
relation
of
the
results
of
the
tests
carried
out
with
different
operators,
test
apparatus
and
in
different
laboratories,
it
is
usually
expressed
in
the
form
of
standard
deviation.
It
is
directly
related
to
the
accuracy
of
the
results
and
MLAs
should
be
able
to
reproduce
the
results
which
are
accepted
worldwide.
Repeatability
is
also
required
in
medical
laboratory
work
as
it
relates
the
ability
of
MLAs
to
carry
out
same
experiment
in
a
similar
manner
and
under
same
conditions
and
to
produce
the
same
results.
4.
What
are
the
process
review
techniques?
There
should
be
some
qualitative
control
tools
which
should
be
designed
to
assess
how
well
and
with
how
much
uniformity
medical
lab
tests
are
being
carried
out
by
MLAs.
The
process
review
techniques
should
be
quick
and
easy
as
it
will
save
the
time
of
quality
control
supervisors.
The
startup
plan
for
the
review
of
the
lab
processes
is
made
on
the
basis
of
guidelines
from
regulatory
and
accredited
organizations
related
to
quality
planning
process.
A
practical
process
review
procedure
will
be
one
which
will
utilize
the
available
tools
and
technology
whether
these
are
analytical
tools
or
these
are
quality
control
procedures.
In
actual
practice,
there
are
two
QC
tools
which
include
Allowable
Total
Error
&
Clinical
Decision
Interval
as
QC
models
are
available
to
extract
the
specifications
for
QC.
One
of
such
tool
is
OPSpecs
chart,
which
is
quite
easy
to
use
&
it
provides
a
visual
representation
of
imprecision
and
inaccuracy
that
is
allowable
for
a
certain
procedure.
Internet
calculators
are
also
available
for
quantitative
assessment
of
the
processes.
With
the
help
of
these
calculators
and
OPSpecs
Allowable
Total
Error
can
be
calculated.
QC
Validator
is
software
which
helps
to
prepare
OPSpecs
charts
for
both
analytical
as
well
as
clinical
quality
requirement
proposes.
It
also
aids
in
the
documentation
of
QC
planning.
5.
Why
calibration
is
important
and
how
to
check
calibration?
For
accuracy
and
precision,
regular
calibration
services
are
required
to
ensure
the
accuracy
of
the
instrument
in
use.
Most
of
the
lab
equipment
manufacturers
have
contracts
with
regular
calibration
groups
to
ensure
that
their
equipment
and
instrumentation
is
working
accurately.
This
is
important
in
maintaining
accuracy
in
the
processes
and
also
to
avoid
legal
consequences
for
not
abiding
the
regional
medical
legislation.
Calibration
is
quite
a
simple
thing
and
it
depends
on
the
nature
of
the
equipment
and
the
process
involved.
Professional
calibration
services
mainly
depend
on
their
own
calibration
procedures
and
calculations
which
are
approved
by
a
certifying,
licensed
compliance
bureau.
Professional
instrumentation
used
for
calibration
services
is
also
checked
for
accuracy
under
strict
conditions.
6.
What
is
the
reporting
procedure
in
the
event
of
deviation?
In
order
to
identify
the
deviations
in
the
calibration,
MLAs
should
have
a
sound
knowledge
of
the
calibration
procedures
and
the
allowable
limits
to
which
error
or
deviation
can
be
accepted.
These
limits
are
provided
at
the
time
of
calibration
by
the
Calibration
Services
provider.
So
in
the
case
if
some
significant
deviation
occurs
then
it
should
be
reported
to
the
department
concerned
with
the
calibration
within
the
institution.
It
will
subsequently
check
the
error
causing
the
deviation
and
will
rectify
the
problem
and
if
the
problem
is
out
of
their
capacity
then
they
will
report
it
to
the
respective
calibration
service
provider
which
will
rectify
the
error
causing
the
deviation.
7.
How
to
deal
with
deviation,
and
who
are
the
relevant
people?
MLAs
should
be
able
to
identify
the
deviations
and
after
deviation
had
occurred
the
following
protocol
should
be
considered
MLAs
should
report
to
the
head
of
the
department
which
in
turn
should
report
the
deviation
to
the
head
of
the
institution
and
the
QC
division
of
the
institution
who
will
send
the
report
in
coordination
with
the
head
of
institution
to
the
corresponding
service
provider
and
they
will
respond
to
the
problem
by
sending
a
team
to
rectify
it
and
after
the
rectification
of
the
deviation,
they
will
submit
a
report
to
both
the
laboratory
officials
as
well
as
the
calibration
service
provider.
8.
What
methods
can
be
used
for
validating
data
and
what
are
the
procedures
for
recording
and
retrieving
data?
MultiQC
is
window
application
software
which
helps
in
validation
of
data
and
it
decreases
the
chances
of
heterogeneity
in
the
results.
It
uses
the
continuous
method
validation
of
data
by
which
it
controls
the
performance
of
all
the
tools
under
it
at
all
the
times.
The
performance
is
always
assessed
in
relation
to
allowable
error
limit.
It
verifies
the
reportable
range
and
clearly
indicate
if
something
fallout
of
this
range.
It
also
does
comparison
of
different
analytical
methods
and
their
tolerance.
Different
regression
tools
are
also
integrated
into
the
software
for
the
validation
of
data.
Usually
for
the
recoding
and
retrieval
of
the
data,
a
computerized
system
is
used.
To
start
with,
a
patient
or
attendant
of
a
patient
comes
with
a
sample
on
which
the
test
is
to
carried
out,
then
the
patient
is
awarded
a
registration
number
which
is
added
in
the
lab
software,
then
the
sample
is
sent
to
the
respective
lab
dept
which
carries
out
the
test
required
and
enters
the
result
in
the
computer
system
against
the
same
patient
number
and
then
the
results
are
given
to
the
patient
by
the
receptionist.
Extreme
precaution
should
be
taken
at
the
time
of
entry
of
the
credentials
as
any
wrong
entry
at
this
time
can
lead
to
false
results
and
also
waste
of
resources.
9.
What
methods
statistical
and
mathematical
techniques
may
be
used
to
evaluate
data?
There
are
mainly
two
statistical
methods
which
are
used
to
assess
the
ability
of
the
test
to
detect
the
disease.
Sensitivity:
It
refers
to
the
ability
of
the
test
to
give
a
positive
result
in
a
patient
who
has
got
the
disease
for
which
the
test
is
performed.
Specificity:
It
refers
to
the
ability
of
the
test
to
give
a
negative
result
for
the
presence
of
a
disease
in
a
patient
who
is
actually
disease
free.
10.
What
methods
can
be
used
to
evaluate
results?
There
are
two
parameters
which
are
widely
used
to
evaluate
the
results.
1.
Accuracy
is
how
close
a
measured
value
is
to
the
actual
(true)
value.
2.
Precision
is
how
close
the
measured
values
are
to
each
other
11.
What
are
the
standard
recording
and
reporting
procedures
to
use?
Results
are
recorded
and
generated
electronically
by
MLAs
and
most
of
the
reports
of
the
results
are
available
are
available
in
less
than
one
and
a
half
hour
time
after
the
reception
of
the
specimen
except
some
more
delicate
tests
which
require
more
time.
Then
these
results
are
reported
through
clinical
information
system
which
will
be
accessible
throughout
the
pathology
department.
In
the
case
when
verbal
communication
of
the
results
is
done
then
following
details
should
be
spoken:
Speaker
Name
&
the
section
concerned,
Patient’s
full
data,
Patient’s
medical
registration
number.
This
information
should
be
read
back
by
the
patient
for
verification
proposes.
Critical
information
should
be
communicated
directly
to
the
concerned
person
to
ensure
that
the
results
are
collected
as
soon
as
possible.
If
despite
of
maximum
efforts
to
communicate
the
results
are
not
collected
then
a
voice
mail
message
can
be
left
for
the
person
concerned.
12.
What
documentation
should
be
used
and
why
it
is
important
to
complete
it
accurately?
Documentation
is
necessary
for
the
compliance
with
the
standard
protocols
and
it
is
the
major
source
of
evidence
for
the
regulatory
authorities,
this
documentation
can
include
mission
statements,
quality
manuals,
laboratory
procedures
as
well
as
the
working
protocols.
It
is
quite
a
time
consuming
procedure
to
devise
this
documentation
but
it
is
mandatory
to
carry
it
out
in
a
systematic
way.
Mainly
four
types
of
documentation
are
needed
in
the
medical
labs
which
include
policies,
procedures,
working
instructions
and
the
forms
and
the
records.
The
significance
of
filling
the
documentation
correctly
relates
to
the
accredition
of
the
particular
lab.
As
these
documents
are
the
material
which
shows
the
working
protocols
which
are
followed
so
in
case
of
any
legal
procedures
these
documents
will
be
required.
In
addition
to
this,
the
higher
authorities
can
check
whether
SOPs
are
followed
or
not
and
these
can
be
proved
with
the
help
of
documentation.
13.
What
operating
conditions
are
necessary
to
conduct
the
investigation?
Operating
conditions
may
differ
according
to
the
nature
of
the
investigation
carried
out
in
the
lab.
At
large
we’ll
have
a
look
at
some
standard
precautionary
measures
which
should
be
followed
in
the
laboratories.
As
most
of
the
lab
tests
are
temperature
dependant
so
temperature
must
be
monitored
closely
and
should
be
fixed
accordingly
for
a
particular
investigation.
Humidity
level
should
also
be
monitored
closely
as
it
can
affect
the
investigations
badly,
complete
aseptic
measures
should
be
adopted
for
the
accurate
results
and
proper
scrubbing
facilities
should
be
available
for
the
MLAs.
Infectious
material
should
be
handled
with
extreme
care
so
as
to
minimize
the
chances
of
spread
of
communicable
diseases.
Additional
operating
instructions
may
be
required
for
different
sort
of
investigations.
All
the
MLAs
should
be
competent
in
operating
the
clinical
information
system
so
that
they
can
do
the
accurate
reporting
of
the
investigations.
14.
What
are
the
essential
features
of
an
investigation
plan,
and
how
to
initiate
it?
Following
are
the
essential
features
of
an
investigation
plan
Request
of
a
particular
investigation
at
the
reception
of
the
lab,
the
entrance
of
the
data
in
CIS
and
the
dispatching
of
the
sample
to
the
concerned
lab
section
which
will
follow
the
SOPs
which
are
documented
for
that
particular
test
and
MLA
will
assure
that
optimum
operating
conditions
are
available
for
the
performance
of
the
tests.
After
the
completion
of
the
test,
MLA
will
inform
the
pathologist
who
will
then
scrutinize
the
results
and
after
his
approval,
these
results
will
be
entered
in
CIS
and
then
these
will
be
delivered
to
the
patients.
15.
How
to
identify
and
deal
with
contingencies?
A
standard
and
an
accredited
laboratory
should
be
able
to
identify
as
well
as
report
any
matter
of
contingency,
so
they
should
coordinate
with
the
respective
college
of
pathology
of
that
particular
country
so
as
to
abide
by
the
reporting
requirements
of
any
reportable
disease
condition,
this
should
be
reported
immediately
by
fax,
mail
or
electronically
as
per
the
regulations.
The
patient
will
also
be
responsible
to
comply
with
the
health
authorities
regarding
the
contingency
issue
and
MLAs
may
be
required
to
give
the
patient
address
to
the
regulatory
authorities.
16.
What
are
the
limits
and
tolerances
of
investigation
techniques?
Each
test
and
investigations
has
its
limitations
and
tolerance
limits.
Tolerance
limits
are
usually
defined
statistically
and
can
be
parametrical
which
considers
that
the
sample
is
taken
from
a
population
which
follows
a
normal
distribution
or
non
parametrical
which
does
not
follow
a
normal
distribution
but
these
are
not
accurate
and
so
cannot
be
relied
upon.
Limitations
of
a
particular
investigation
relate
its
ability
to
detect
a
particular
disorder.
There
are
certain
investigation
which
can
aid
in
the
diagnosis
of
a
disease
whereas
on
the
other
side
there
are
some
investigations
which
do
not
aid
in
the
diagnosis
but
can
aid
in
determining
the
prognosis
of
the
disease
and
the
response
to
the
treatment.
17.
What
units
of
measurement
are
required?
The
units
of
measurement
vary
and
depend
on
the
type
of
investigation
carried
out;
usually
metric
system
is
used
to
express
the
quantities.
Mass
is
expressed
in
grams,
volume
is
expressed
in
liters
and
the
length
is
expressed
in
terms
of
meters.
One
of
the
advantage
of
the
metric
system
is
that
is
based
on
the
multiples
of
10
which
makes
the
calculations
easy
and
it
is
accepted
universally.
Other
units
can
also
be
used
for
example
moles
or
milli
moles
and
different
formulae
are
also
available
with
the
help
of
which
one
unit
can
be
converted
into
equivalent
other
unit.
18.
What
methods
can
be
used
for
report
writing?
Following
portions
should
be
included
in
a
comprehensive
medical
lab
report;
at
first
the
patient
description
of
the
disease
is
to
be
mentioned
in
patients
own
words
which
may
aid
in
establishing
the
diagnosis
along
with
the
lab
investigations;
write
your
physical
findings
correctly;
give
all
the
required
information
which
is
extracted
from
the
test
performed
and
also
mention
the
limitations
of
that
particular
test
and
recommend
if
there
is
any
other
investigation
or
procedure
which
may
add
in
the
diagnosis
in
addition
to
the
investigation
which
is
carried
out,
correlate
the
clinical
findings
with
the
lab
investigation
result.
19.
Who
are
the
relevant
people
in
the
organisation?
These
include
the
following
people
Receptionist,
Phlebotomist,
Computer
Operator,
MLAs,
Lab
Technicians,
QC
Supervisors,
Pathologist
(Clinical,
Chemical,
Forensic),
Hematologist
20.
What
could
be
the
legal
consequences
of
breaches
of
quality
procedures?
In
case
of
non
compliance
or
breaches
of
the
standard
procedures,
the
registration
of
the
lab
can
be
suspended
and
the
license
of
the
lab
can
be
cancelled.
The
patient
or
the
patient
insurance
agency
can
initialize
legal
proceedings
against
the
lab
or
in
milder
cases;
the
lab
can
be
put
on
probation
and
will
be
supervised
for
a
certain
period
of
time
so
MLAs
should
be
well
aware
of
all
the
SOPs
as
well
as
the
legal
consequences
so
as
to
minimize
the
occurrence
of
such
incidents.
21.
What
evaluation
criteria
should
be
used
that
is
relevant
to
customer
requirements?
Mainly
the
customers
require
the
knowledge
of
the
normal
values
for
a
particular
test
so
one
of
the
thing
which
needs
continuous
evaluation
is
the
reference
values
for
the
customers
and
these
should
be
from
current
literature
and
should
be
scrutinized
regularly,
MLAs
should
make
sure
that
the
prevalence
rates
of
different
tests
should
be
noted
and
regular
evaluation
of
the
results
of
the
investigations
as
well
as
any
deviation
or
any
error
which
exceeds
Allowable
Medical
Error
should
be
monitored
closely
22.
What
methods
should
be
used
for
feedback?
On
behalf
of
laboratory,
complete
details
of
all
the
means
of
communication
such
as
Phone,
Fax,
e-
mail,
Mobile
Number
as
well
as
the
website
address
of
the
lab
should
be
clearly
written
on
the
report
and
on
the
other
hand
all
these
contacting
details
should
be
taken
from
the
patient
also
and
should
be
entered
in
the
Clinical
Information
System
at
the
time
of
patient’s
record
entrance.
In
addition
to
this,
regular
feed
back
forms
should
be
sent
to
the
institutions
which
are
sending
the
patients
regularly
to
the
lab.
23.
The
relevant
roles
and
responsibilities
of
yourself
and
others
under
the
health
and
safety
at
work
act
1974
and
current
legislation
(e.g.
management
of
health
and
safety
at
work
regulation;
workplace
health
and
safety
and
welfare
regulation;
personal
protection
at
work
regulation
;
manual
handling
operations
regulations;
provision
and
use
of
work
equipment).
MLAs
should
make
sure
that
there
is
no
emission
of
noxious
or
poisonous
material
into
the
air.
All
the
employees
should
not
be
involved
in
the
misuse
of
any
of
the
material
present
in
the
lab;
everyone
should
behave
responsibly
to
ensure
the
safety
of
him
as
well
as
the
safety
of
the
other
working
at
the
same
place.
Manual
handling
of
the
materials
and
the
equipments
should
be
minimized
and
in
the
case
where
it
cannot
be
avoided
then
proper
measures
should
be
taken
to
ensure
the
personal
protection.
24.
How
to
locate
relevant
health
and
safety
information
for
your
tasks and the sources of expert assistance when help is needed? This information can be gathered or
search from the local medical regulation manual as well as such information is available on the net on
the
websites run by the state authorities which define the health laws such as the State Department Of
health. If some problem arises while doing a particular investigation and the problem is above the
comprehension of the involved MLA then that MLA should be able to contact the pathologist at that
time
or
contact the QC supervisor if the matter relates to the quality control. The updated directory should
be
present
in
the
laboratory
through
which
MLA
can
contact the higher officials for expert advice. 25. What constitutes a hazard in the workplace (such as
moving parts of machinery, electricity, slippery and uneven surfaces, dust and fumes, handling and
transporting, contaminants and irritants, material ejection, fire, working at height, environment,
pressure/stored energy system, volatile or toxic material, unshielded processes). Careful handling
should
be
done
when
the
movement of delicate lab instruments is taking place to prevent the breakage as well as to avoid
damage to the machinery. Continuous electrical supply should be ensured as well as the sockets
should
be
kept away from the humid surfaces. Slippery and uneven surfaces should be covered with smooth
and
flat blocks to avoid inaccuracy in readings and spillage. Proper ventilation system with powerful
exhaust system should be there to pump out the toxic fumes. Contaminants and the irritants should
be
disposed off properly and to a safe place away from the public area. Proper dressing should be worn
while doing a specific test and toxic materials should be dealt with extreme care. 26. What are your
responsibilities
for
dealing with hazards and reducing risks in workplace? In case of any hazard related to the
laboratory
materials
and
the
equipment, MLAs should ensure the following: Immediately inform the concerned national
authorities
and
Disaster Management System. Evacuation of all the personnel from the vicinity, sealing off the work
place to minimize the chances of spread of the contamination and help the people doing the disaster
management. To reduce the risk of such an event, national guidelines regarding transportation and
handling
of
lab
equipment
should
be
followed. 27. What are the risks associated with your working environment, the tools, materials and
equipment
that
you
use, spillages of oil and chemicals, not reporting accidental breakages of tools or equipment and not
following
laid down working practice and procedure? As in the laboratory, acid and basic substances are used
which
if
not
handled
properly
can
cause burns and their spillage can also damage the other instruments. If accidental breakages are not
reported
then
these
can
lead
to
fatal damages by spillage while performing the test being unaware of the breakage. If the SOPs are
not
followed
then
the
quality
control
can
be
compromised and as a consequence legal consequences can be seen. 28. What constitutes dangerous
occurrences and hazardous malfunctions and why these must be reported even when no one was
injured? Dangerous situations can arise due to; Breakage, spillage, unsupervised transportation of
chemicals, careless handling of the lab equipment, contamination of the laboratory and its spread to
outside environment. Malfunction may include improperly working electrical socket, ineffective
pumping of the fumes and dust out of the laboratory resulting in the accumulation of poisonous
fumes inside the lab. These incidents should be reported to concerned authorities at the institution as
well
as
national level immediately regardless of the casualties or the number of injured to ensure that such
incidents may not occur in the future and proper actions should be implemented by the concerned
authorities
to
prevent such occurrences. 29. What the organizational policy is with regard to fire fighting
procedures,
the
common causes of fire and what you can do to help prevent them? Basically there are five steps in
fire fighting which include rescue operations, protecting the building and the equipment within the
vicinity of the fire from the damage, making the fire stay put , try to extinguish it with fire
extinguishers and then carry out the salvage procedures. An officer should be made in charge of the
proceedings
and
he should be experienced person who can decide the best strategy to fight the fire. The operation
must
be
such
that
it
ensures the safety of both the fire fighters as well as the people caught in the fire. In medical labs,
the
usual causes of the fire includes short circuiting, gas leakage from the burners, uncontrolled
exothermic chemical reactions and accumulation of the inflammable fumes and their reaction with
the
chemicals present in the lab so proper guidelines should be followed and required measures should
be
taken
while dealing with inflammable materials, ensure proper working of the ventilation system and
regular
assessment
of
the
electrical supply of the lab. 30. How to lift and carry loads safely and the annual and mechanical aids
available? As most of the lab equipment is glass ware and in turn is fragile so these should be
transported with extreme care in specialized containers with the help of transporters which can move
within
the
lab.
These
vehicles meant for the transport of lab equipment can be rented upon from different companies
which
are
specialized in the transportation of the lab equipment. 31. How to prepare and maintain safe working
areas, standards and procedures to ensure good housekeeping? Following measures should be taken
to
maintain safe working areas Each worker should have at least 18.6 m2 of space with 3 m run of
benching and 24 m of free air space, floors should be resistant to slipping, seamless, be impermeable
to
liquids and resistant to most, if not all chemicals that are normally used in laboratories. The exteriors
of
partitions and walls should be smooth, impermeable and easily cleaned. Windows should be sealable
and
fitted with blinds. Ventilation system should be adequate to deal with any accident. MLAs should be
well
aware
of
the
stock present within the lab and should report shortage of any substance before time so as to prevent
the
delay in the investigation due to unavailability of resources. On the other hand, MLAs should also
make
sure
that
the
stocks are bought according to the requirement as excessive stock of less frequently used chemicals
may
lead
to
wastage of resources. Read More Motivated employees are more committed to their work • praise •
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