Good Manufacturing Practices (GMP) Guidelines: Visit For More Ppt's & Material

GOOD MANUFACTURING
PRACTICES(GMP)
GUIDELINES
Visit
www.bpharmstuf.com
For more ppt’s & material
CONTENTS
DEFINATION OF GMP
PRINCIPLES OF GMP
IMPORTANCE OF GMP
INTERRELATIONSHIPS OF QA,QC,GMP
IMPORTANT DOCUMENTS IN GMP
ATTRIBUTES OF GOOD DOCUMENTS
GENERAL PROVISIONS
1.BUILDING&FACILITIES
2.EQUIPMENTS
www.bpharmstuf.com 2
3.Production&process control
4.Packaging&labelling control
5.Handling&distribution
6.Labaratory control
7.Records&reports
 Conclusions
 References
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.
What is cGMP ?
Usually see “cGMP” – where c = current, to emphasize
that the expectations are dynamic
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
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.
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.
Why GMP is important:
o A poor quality medicine may contain toxic substances

that have been unintentionally added.
o A medicine that contains little or none of the claimed

ingredient will not have the intended therapeutic effect.
GMP helps boost pharmaceutical export
opportunities:
Most countries will only accept import and sale of
medicines that have been manufactured to
internationally recognized GMP.
Governments seeking to promote their countries

export of pharmaceuticals can do so by making
GMP mandatory for all pharmaceutical production
and by training their inspectors in GMP
requirements.
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.
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!
QA, GMP & QC inter-relationship:
It is the sum total of theQA

organized arrangements with
the objective of ensuring that products will be of the
quality required for their intended use
Inter-relationship of
QA,GMP&QC:
Is that part of Quality Assurance
GMP aimed at ensuring that
products are consistently manufactured to a quality
appropriate to their intended use
QA, GMP & QC inter-relationship:
Is that part of GMP concerned with sampling,

QCdocumentation & release
specification & testing,
procedures which ensure that the necessary &
relevant tests are performed & the product is
released for use only after ascertaining it’s quality
QC and QA:
QC is that part of GMP
which is concerned with QA is the sum total of
sampling, organized arrangements
specifications, testing and made with the object of
with in the organization, ensuring that product
documentation,and release will be of the Quality
procedures which ensure required by their
that the necessary and intended use.
relevant tests are carried out
QC and QA:
Operational laboratory All those planned or

techniques and activities systematic actions
used to fulfill the necessary to provide
requirement of Quality adequate confidence that
a product will satisfy the
requirements for quality
QC and QA:
 QC is lab based  QA is company based
GMP:
GMP in solid dosage forms

GMP in semisolid dosage forms
GMP in Liquid orals
GMP in Parenterals Production
GMP in Ayurvedic medicines
GMP in Bio technological products
GMP in Nutraceuticals and cosmeceuticals
GMP in Homeopathic medicines
Ten Principles of GMP:
1. Design and construct the facilities and equipments
properly
2. Follow written procedures and Instructions
3. Document work
4. Validate work
5. Monitor facilities and equipment
6. Write step by step operating procedures and work on
instructions
7. Design ,develop and demonstrate job competence
8. Protect against contamination
9. Control components and product related processes
10. Conduct planned and periodic audits
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
Cost of effective GMP:
In fact Cost benefits – positive cost benefits of
GMP/QA
Good plant lay out, Smooth work flows, Efficient

documentation systems, well controlled process,
good stores lay outs and stores records- These are
Good manufacturing practices
Reduction in work in process and inventory holding

costs
Avoidance of cost of Quality failure ( cost of waste, of

rework, of recall, of consumer compensation and of
loss of company reputation)
List of important documents in GMP:
Policies
SOP
Specifications
 MFR (Master Formula Record)
BMR
Manuals
Master plans/ files
Validation protocols
Forms and Formats
Records
10 attributes of a good document:
1. Accurate
2. Clear
3. Complete
4. Consistent
5. Indelible
6. Legible
7. Timely
8. Direct
9. Authentic
10. Authorized
How do GMPs of different countries compare?
At a high level, GMPs of various nations are very similar;

most require things like:
 Equipment and facilities being properly

designed, maintained, and cleaned
 Standard Operating Procedures (SOPs) be
written and approved
 An independent Quality unit (like Quality
Control and/or Quality Assurance)
 Well trained personnel and management
cGMP For Finished Pharmaceuticals:
1. General Provision
2. Organization & Personnel
3. Building & Facilities
4. Equipment
5. Control of Components & Drug Product Containers
& Closures
6. Production & Process Control
7. Packaging & Labeling Control
8. Handling & Distribution
9. Laboratory Control
10. Records & Reports
11. Returned & Salvaged Drugs
General Provision:
1. Scope
2. Definitions
Building & Facilities:
1. Design and construction features.

2. Lighting.
3. Ventilation, air filtration, air heating and cooling.
4. Plumbing.
5. Sewage and refuse.
6. Washing and toilet facilities.
7. Sanitation.
8. Maintenance.
Equipment:
1. Equipment design, size, and location.

2. Equipment construction.
3. Equipment cleaning and maintenance.
4. Automatic, mechanical, and electronic equipment.
5. Filters.
Control of Components & Drug
Product Containers & Closures:
1. General requirements.
2. Receipt & storage of untested components, drug product
containers, and closures.
3. Testing and approval or rejection of components, drug
product containers, and closures.
4. Use of approved components, drug product containers,
and closures.
5. Retesting of approved components, drug product
containers, and closures.
6. Rejected components, drug product containers, and
closures.
7. Drug product containers and closures.
Production & Process Control:
1. Written procedures; deviations.

2. Charge-in of components.
3. Calculation of yield.
4. Equipment identification.
5. Sampling and testing of in-process materials
and drug products.
6. Time limitations on production.
7. Control of microbiological contamination.
8. Reprocessing.
Packaging & Labeling Control
1. Materials examination and usage criteria.

2. Labeling issuance.
3. Packaging and labeling operations.
4. Tamper-evident packaging requirements for over-
the-counter (OTC) human drug products.
5. Drug product inspection.
6. Expiration dating.
Handling & Distribution:
1. Warehousing procedures.
2. Distribution procedures.
Laboratory Control:
2. Testing and release for distribution.
3. Stability testing.
4. Special testing requirements.
5. Reserve samples.
6. Laboratory animals.
7. Penicillin contamination.
Records & Reports:
2. Equipment cleaning and use log.
3. Component, drug product container, closure, and
labeling records.
4. Master production and control records.
5. Batch production and control records.
6. Production record review.
7. Laboratory records.
8. Distribution records.
9. Complaint files.
Returned & Salvaged Drug Products:
1. Returned drug products.

2. Drug product salvaging.
CONCLUSIONS:
For the time being, the approach is

different but the
principles are much the same: a
complete and
operative Quality System
demonstrating that there is overall
control.
• References
• Notes
^ U.S. Food and Drug Administration (2007-06-22).
"FDA Issues Dietary Supplements Final Rule". Press
release.
http://www.fda.gov/NewsEvents/Newsroom/PressAnnou
ncements/2007/ucm108938.htm
. Retrieved 2010-06-04.
^ Pharmaceutical Press.
"Rules and Guidance for Pharmaceutical Manufacturers a
nd Distributors - Edition: 2007"
Retrieved 2010-03-01.
^ http://mohfw.nic.in/
 Bankar
 Lachman
 ansel
Q
AN
TH
Thank you for
Listening
Any Queries??
www.bpharmstuf.com
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GOOD MANUFACTURING

"GMP" - A set of principles and procedures which,

 Quality Safety Efficacy X

A basic tenet of GMP is that quality cannot be

It is designed to minimize the risks involved in any

unexpected contamination of products, causing damage

incorrect labels on containers, which could mean that

insufficient or too much active ingredient, resulting in

o A poor quality medicine may contain toxic substances

o A medicine that contains little or none of the claimed

Governments seeking to promote their countries

Detailed, written procedures are essential for each process

There must be systems to provide documented proof that

 GMP is the magic key that opens the door of the

 In matter of GMP, swim with the current and in

It is the sum total of theQA

Is that part of GMP concerned with sampling,

Operational laboratory All those planned or

 QC is lab based  QA is company based

GMP in solid dosage forms

Reduce pollution - Zero discharge

Good plant lay out, Smooth work flows, Efficient

Reduction in work in process and inventory holding

Avoidance of cost of Quality failure ( cost of waste, of

At a high level, GMPs of various nations are very similar;

 Equipment and facilities being properly

1. Design and construction features.

1. Equipment design, size, and location.

1. Written procedures; deviations.

1. Materials examination and usage criteria.

1. Returned drug products.

For the time being, the approach is

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