GMP (Good Manufacturing Practices) are procedures and principles that help ensure pharmaceutical products are consistently produced and controlled according to quality standards appropriate for their intended use. A key principle of GMP is that quality must be built into every step of the manufacturing process rather than tested into the final product. GMP guidelines cover all aspects of production from facilities and equipment to staff training to ensure minimum risks like contamination, incorrect labeling, or insufficient active ingredients. Strict adherence to GMP procedures and documentation is important to ensure medicines are safe, effective and meet their intended purpose.

1. Introduction toGMP
By
V.SARAVANAN

2. What is GMP ?

GMP is that part of Quality assurance
which ensures that the products are
consistently manufactured and controlled
to the Quality standards appropriate to
their intended use

"GMP" - A set of principles and procedures
which, when followed by manufacturers
for therapeutic goods, helps ensure that
the products manufactured will have the
required quality.
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3. Quality Definition
 Quality
of a medicinal product is
measured by it’s fitness for purpose .
Safety and efficacy are not separable
from Quality but part of it

Quality
Safety
Efficacy
X
Quality
Safety Efficacy
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4. 22/10/2008
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5. Good Manufacturing Practices

A basic tenet of GMP is that quality cannot
be tested into a batch of product but must
be built into each batch of product during
all stages of the manufacturing process.

It is designed to minimize the risks
involved in any pharmaceutical production
that cannot be eliminated through testing
the final product.
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6. Some of the main risks are
– unexpected contamination of products, causing
damage to health or even death.
– incorrect labels on containers, which could
mean that patients receive the wrong
medicine.
– insufficient or too much active ingredient,
resulting in ineffective treatment or adverse
effects.
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7. Why GMP is important
– A poor quality medicine may contain
toxic substances that have been
unintentionally added.
– A medicine that contains little or none of
the claimed ingredient will not have the
intended therapeutic effect.
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8. GMP Covers…

ALL aspects of production; from the starting
materials, premises and equipment to the
training and personal hygiene of staff.

Detailed, written procedures are essential for
each process that could affect the quality of the
finished product.

There must be systems to provide documented
proof that correct procedures are consistently
followed at each step in the manufacturing
process - every time a product is made.
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9. GMP
 The
Quality of a formulation or a
bulk drug depends on the Quality of
those
producing it
 GMP is the magic key that opens the
door of the Quality
 In matter of GMP, swim with the
current and in matter of Quality
stand like a rock!
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10. QA, GMP & QC inter-relationship
QA
GMP
QC
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11. QA, GMP & QC inter-relationship
QA
It is the sum total of the
organized arrangements
with the objective of
ensuring that products
will be of the quality
required for their
intended use
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12. QA, GMP & QC inter-relationship
GMP
Is that part of Quality
Assurance aimed at
ensuring that products
are consistently
manufactured to a
quality appropriate to
their intended use
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13. QA, GMP & QC inter-relationship
QC
Is that part of GMP concerned
with sampling, specification
& testing, documentation &
release procedures which
ensure that the necessary &
relevant tests are performed
& the product is released for
use only after ascertaining
it’s quality
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14. QC and QA

QC is that part of GMP  QA is the sum total
which is concerned with
of organized
sampling,
arrangements
specifications, testing
made with the
and with in the
object of ensuring
organization,
that product will be
documentation,and
of the Quality
release procedures
which ensure that the
required by their
necessary and relevant
intended use.
tests are carried out
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15. QC and QA

QC is lab based
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
QA is company
based
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16. GMP guidelines

GMP as per Schedule “M”
www.cdsco.nic.in

GMP as per WHO
www.who.int

GMP as per MCA now known as MHRA
www.mca.gov.uk

GMP as per TGA
www.tga.gov.au

GMP as per US FDA
www.fda.gov

GMP as per ICH guidelines
www.ich.org
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17. GMP
 Good
Manufacturing Practice
 Good Management Practice
 Get More Profit
 Give more Production
 GMP Training with out tears
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18. Ten Principles of GMP
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
Design and construct the facilities and
equipments properly
Follow written procedures and Instructions
Document work
Validate work
Monitor facilities and equipment
Write step by step operating procedures and
work on instructions
Design ,develop and demonstrate job
competence
Protect against contamination
Control components and product related
processes
Conduct planned and periodic audits
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19. Beyond GMP
 Reduce
pollution - Zero discharge
 Adaptation of environment friendly
methods
 Consideration for better and
healthier life tomorrow
 Consideration of ethics in life
 One should begin with end in mind
otherwise it will be the beginning of
the end
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20. List of important documents in GMP










Policies
SOP
Specifications
MFR (Master Formula Record)
BMR
Manuals
Master plans/ files
Validation protocols
Forms and Formats
Records
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21. 10 attributes of a good document
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
Accurate
Clear
Complete
Consistent
Indelible
Legible
Timely
Direct
Authentic
Authorized
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22. Certifying agencies
 ICH. www.ich.org
 WHO. www.who.int
 US
FDA. www.fda.gov
 EU/EMEA. www.emea.europa.eu
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23. cGMP For Finished Pharmaceuticals
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
General Provision
Organization & Personnel
Building & Facilities
Equipment
Control of Components & Drug
Product Containers & Closures
Production & Process Control
Packaging & Labeling Control
Handling & Distribution
Laboratory Control
Records & Reports
Returned & Salvaged Drugs
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24. Control of Components & Drug
Product Containers & Closures
1.
2.
3.
4.
5.
6.
7.
General requirements.
Receipt & storage of untested components,
drug product containers, and closures.
Testing and approval or rejection of
components, drug product containers, and
closures.
Use of approved components, drug product
containers, and closures.
Retesting of approved components, drug
product containers, and closures.
Rejected components, drug product containers,
and closures.
Drug product containers and closures.
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25. Production & Process Control
1.
2.
3.
4.
5.
6.
7.
8.
Written procedures; deviations.
Charge-in of components.
Calculation of yield.
Equipment identification.
Sampling and testing of in-process
materials and drug products.
Time limitations on production.
Control of microbiological contamination.
Reprocessing.
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26. Packaging & Labeling Control
1.
2.
3.
4.
5.
6.
Materials examination and usage
criteria.
Labeling issuance.
Packaging and labeling operations.
Tamper-evident packaging
requirements for over-the-counter
(OTC) human drug products.
Drug product inspection.
Expiration dating.
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27. Laboratory Control
1.
2.
3.
4.
5.
6.
7.
General requirements.
Testing and release for distribution.
Stability testing.
Special testing requirements.
Reserve samples.
Laboratory animals.
Penicillin contamination.
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28. Records & Reports
1.
2.
3.
4.
5.
6.
7.
8.
9.
General requirements.
Equipment cleaning and use log.
Component, drug product container, closure,
and labeling records.
Master production and control records.
Batch production and control records.
Production record review.
Laboratory records.
Distribution records.
Complaint files.
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29. THANK YOU
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