g m p 01

Introduction toGMPIntroduction toGMP

V.SARAVANANV.SARAVANANBy

22/10/200822/10/2008 Department of PharmaceuticsDepartment of Pharmaceutics 22

What is GMP ?What is GMP ?

GMP is that part of Quality assurance GMP is that part of Quality assurance which ensures that the products are which ensures that the products are consistently manufactured and controlled consistently manufactured and controlled to the Quality standards appropriate to to the Quality standards appropriate to their intended usetheir intended use

"GMP""GMP" - A set of principles and procedures - A set of principles and procedures which, when followed by manufacturers which, when followed by manufacturers for therapeutic goods, helps ensure that for therapeutic goods, helps ensure that the products manufactured will have the the products manufactured will have the required quality.required quality.


Quality DefinitionQuality Definition

Quality of a medicinal product is Quality of a medicinal product is measured by it’s fitness for purpose . measured by it’s fitness for purpose . Safety and efficacy are not separable Safety and efficacy are not separable from Quality but part of itfrom Quality but part of it

Quality Safety Efficacy XQuality Safety Efficacy X

QualityQuality Safety EfficacySafety Efficacy


Good Manufacturing PracticesGood Manufacturing Practices

A basic tenet of GMP is that quality cannot A basic tenet of GMP is that quality cannot be tested into a batch of product but must be tested into a batch of product but must be built into each batch of product during be built into each batch of product during all stages of the manufacturing process.all stages of the manufacturing process.

It is designed to minimize the risks It is designed to minimize the risks involved in any pharmaceutical production involved in any pharmaceutical production that cannot be eliminated through testing that cannot be eliminated through testing the final product.the final product.


Some of the main risks areSome of the main risks are

– unexpected contamination of products, causing unexpected contamination of products, causing damage to health or even death. damage to health or even death.

– incorrect labels on containers, which could incorrect labels on containers, which could mean that patients receive the wrong mean that patients receive the wrong medicine.medicine.

– insufficient or too much active ingredient, insufficient or too much active ingredient, resulting in ineffective treatment or adverse resulting in ineffective treatment or adverse effects.effects.


Why GMP is importantWhy GMP is important

– A poor quality medicine may contain A poor quality medicine may contain toxic substances that have been toxic substances that have been unintentionally added. unintentionally added.

– A medicine that contains little or none of A medicine that contains little or none of the claimed ingredient will not have the the claimed ingredient will not have the intended therapeutic effect. intended therapeutic effect.


GMP Covers…GMP Covers…

ALLALL aspects of production; from the starting aspects of production; from the starting materials, premises and equipment to the materials, premises and equipment to the training and personal hygiene of staff.training and personal hygiene of staff.

Detailed, written procedures are essential for Detailed, written procedures are essential for each process that could affect the quality of the each process that could affect the quality of the finished product. finished product.

There must be systems to provide documented There must be systems to provide documented proof that correct procedures are consistently proof that correct procedures are consistently followed at each step in the manufacturing followed at each step in the manufacturing process - every time a product is made.process - every time a product is made.


GMPGMP

The Quality of a formulation or a bulk The Quality of a formulation or a bulk drug depends on the Quality of thosedrug depends on the Quality of those

producing itproducing it GMP is the magic key that opens the GMP is the magic key that opens the

door of the Qualitydoor of the Quality In matter of GMP, swim with the In matter of GMP, swim with the

current and in matter of Quality current and in matter of Quality stand like a rock!stand like a rock!


QA, GMP & QC inter-relationship

QC

GMP

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

QA



Is that part of Quality Assurance aimed at

ensuring that products are consistently

manufactured to a quality appropriate to

their intended use

GMP



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

QC


QC and QAQC and QA

QC is that part of GMP QC is that part of GMP which is concerned which is concerned with sampling,with sampling,

specifications, testing specifications, testing and with in the and with in the organization, organization, documentation,and documentation,and release procedures release procedures which ensure that the which ensure that the necessary and relevant necessary and relevant tests are carried outtests are carried out

QA is the sum total QA is the sum total of organized of organized arrangements arrangements made with the made with the object of ensuring object of ensuring that product will be that product will be of the Quality of the Quality required by their required by their intended use.intended use.


QC and QAQC and QA

QC is lab based QC is lab based QA is company QA is company basedbased


GMP guidelinesGMP guidelines GMP as per Schedule “M”GMP as per Schedule “M” www.cdsco.nic.inwww.cdsco.nic.in

GMP as per WHOGMP as per WHO www.who.intwww.who.int

GMP as per MCA now known as MHRAGMP as per MCA now known as MHRA www.mca.gov.ukwww.mca.gov.uk

GMP as per TGAGMP as per TGA www.tga.gov.auwww.tga.gov.au

GMP as per US FDAGMP as per US FDA www.fda.govwww.fda.gov GMP as per ICH guidelinesGMP as per ICH guidelines www.ich.orgwww.ich.org


GMPGMP

Good Manufacturing PracticeGood Manufacturing Practice Good Management PracticeGood Management Practice Get More ProfitGet More Profit Give more ProductionGive more Production GMP Training with out tearsGMP Training with out tears


Ten Principles of GMPTen Principles of GMP1.1. Design and construct the facilities and Design and construct the facilities and

equipments properlyequipments properly2.2. Follow written procedures and InstructionsFollow written procedures and Instructions3.3. Document workDocument work4.4. Validate workValidate work5.5. Monitor facilities and equipmentMonitor facilities and equipment6.6. Write step by step operating procedures and Write step by step operating procedures and

work on instructionswork on instructions7.7. Design ,develop and demonstrate job Design ,develop and demonstrate job

competencecompetence8.8. Protect against contaminationProtect against contamination9.9. Control components and product related Control components and product related

processesprocesses 10.10. Conduct planned and periodic auditsConduct planned and periodic audits


Beyond GMPBeyond GMP

Reduce pollution -Reduce pollution - Zero discharge Zero discharge Adaptation of environment friendly Adaptation of environment friendly

methodsmethods Consideration for better and Consideration for better and

healthier life tomorrowhealthier life tomorrow Consideration of ethics in lifeConsideration of ethics in life One should begin with end in mind One should begin with end in mind

otherwise it will be the beginning of otherwise it will be the beginning of the end the end


List of important documents in GMPList of important documents in GMP

PoliciesPolicies SOPSOP SpecificationsSpecifications MFR (Master Formula Record)MFR (Master Formula Record) BMRBMR ManualsManuals Master plans/ filesMaster plans/ files Validation protocolsValidation protocols Forms and FormatsForms and Formats RecordsRecords


10 attributes of a good document10 attributes of a good document

1.1. AccurateAccurate2.2. ClearClear3.3. CompleteComplete4.4. ConsistentConsistent5.5. IndelibleIndelible6.6. LegibleLegible7.7. TimelyTimely8.8. Direct Direct 9.9. AuthenticAuthentic10.10. AuthorizedAuthorized


Certifying agenciesCertifying agencies

ICH.ICH. www.ich.orgwww.ich.org

WHO. WHO. www.who.intwww.who.int

US FDA.US FDA. www.fda.govwww.fda.gov

EU/EMEA.EU/EMEA. www.emea.europa.euwww.emea.europa.eu


cGMP For Finished PharmaceuticalscGMP For Finished Pharmaceuticals

1.1. General ProvisionGeneral Provision2.2. Organization & PersonnelOrganization & Personnel3.3. Building & FacilitiesBuilding & Facilities4.4. EquipmentEquipment5.5. Control of Components & Drug Product Control of Components & Drug Product

Containers & ClosuresContainers & Closures6.6. Production & Process ControlProduction & Process Control7.7. Packaging & Labeling ControlPackaging & Labeling Control8.8. Handling & DistributionHandling & Distribution9.9. Laboratory ControlLaboratory Control10.10. Records & ReportsRecords & Reports11.11. Returned & Salvaged DrugsReturned & Salvaged Drugs


Control of Components & Drug Control of Components & Drug Product Containers & ClosuresProduct Containers & Closures

1.1. General requirements. General requirements. 2.2. Receipt & storage of untested components, Receipt & storage of untested components,

drug product containers, and closures. drug product containers, and closures. 3.3. Testing and approval or rejection of Testing and approval or rejection of

components, drug product containers, and components, drug product containers, and closures. closures.

4.4. Use of approved components, drug product Use of approved components, drug product containers, and closures. containers, and closures.

5.5. Retesting of approved components, drug Retesting of approved components, drug product containers, and closures. product containers, and closures.

6.6. Rejected components, drug product containers, Rejected components, drug product containers, and closures.and closures.

7.7. Drug product containers and closures. Drug product containers and closures.


Production & Process ControlProduction & Process Control

1.1. Written procedures; Written procedures; deviationsdeviations. . 2.2. Charge-in of components.Charge-in of components.3.3. Calculation of yield. Calculation of yield. 4.4. Equipment identification.Equipment identification. 5.5. Sampling and testing of in-process Sampling and testing of in-process

materials and drug products. materials and drug products. 6.6. Time limitations on production. Time limitations on production. 7.7. Control of microbiological contamination.Control of microbiological contamination.8.8. Reprocessing. Reprocessing.


Packaging & Labeling ControlPackaging & Labeling Control

1.1. Materials examination and usage Materials examination and usage criteria.criteria.

2.2. Labeling issuance. Labeling issuance. 3.3. Packaging and labeling operations.Packaging and labeling operations. 4.4. Tamper-evident packaging Tamper-evident packaging

requirements for over-the-counter requirements for over-the-counter (OTC) human drug products. (OTC) human drug products.

5.5. Drug product inspection. Drug product inspection. 6.6. Expiration dating. Expiration dating.


Laboratory ControlLaboratory Control

1.1. General requirements.General requirements.

2.2. Testing and release for distribution. Testing and release for distribution.

3.3. Stability testing.Stability testing.

4.4. Special testing requirements.Special testing requirements.

5.5. Reserve samples. Reserve samples.

6.6. Laboratory animals. Laboratory animals.

7.7. Penicillin contamination. Penicillin contamination.

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Records & ReportsRecords & Reports

1.1. General requirements. General requirements. 2.2. Equipment cleaning and use log. Equipment cleaning and use log. 3.3. Component, drug product container, closure, Component, drug product container, closure,

and labeling records.and labeling records. 4.4. Master production and control records.Master production and control records. 5.5. Batch production and control records. Batch production and control records.

6.6. ProductionProduction record review. record review. 7.7. Laboratory records. Laboratory records. 8.8. Distribution records. Distribution records. 9.9. Complaint files. Complaint files.

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THANK YOUTHANK YOU

g m p 01

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