Current Good Manufacturing practices is used for the production for the medicinal product.

1. cGMPs According to US FDA
Good Manufacturing Practice (GMP) ensures that quality is built into the organisation and processes
involved in manufacture GMP covers all aspects of“manufacture”including collection, transportation,
processing,storage,quality control and delivery of the finished product.
It is designed to minimize the risks involved in any pharmaceutical production that cannot be
eliminated through testing the final product Protect the integrity and quality of manufactured product
intended for human use.
PRINCIPLES OF cGMP:
 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
LIST OF IMPORTANT DOCUMENTS IN cGMP:
 Policies
 SOP
 Specifications
 MFR (MasterFormula Record)
 Batch Package Records (BMR)
 Manuals
 Masterplans/ files
 Validation protocols
 Forms and Formats
 Records
cGMPs cover a broad range of methods, practices and principles that are implemented and documented
during product development to ensure consistent manufacture of quality products.
the cGMP assures the identity, strength, quality, and purity of drug products is built into the design and
manufacturing process at every step.
GMP is a dynamic concept and practice. Staying “current” is driven by technology, improved practices
and regulatory issues.
USFDA REGULATIONS:-
1. The requirements for compliance to cGMP are lain down in the following code of Federal
Regulation (21CFR).
2. 21 CFR Part 210 cGMP in manufacturing, processing,packing, or holding of the drugs
3. 21 CFR Part 211 cGMP for finished pharmaceutical.
4. 21 CFR Part 610 – Current Good Manufacture of Biological Products
5. 21 CFR Part 820 – Current Good Manufacturing Practices for Devices
Essential elements of cGMP are:-

2. 1. Good Documentation Practices
2. Training
3. Facilities and Equipment Management
4. Change Control Systems
5. Operations Oversight and Management
cGMP covers:- General consideration, Personal, premises, Equipment, Sanitation, sop's Raw material,
self inspection & audit, MFR, BMR, warehousing area, labels & otherprinters Material, Qc
CGMP for finished pharmaceuticals: part 211
A. Subpart A - General Provision
Scope:- The minimum cGMP for preparation of drug products for administration to humans or animals.
The requirements in this part shall not be enforced for OTC drug products and all their ingredients are
ordinarily marketed and consumed as human foods.
Definitions:-The definitions and interpretations contained in section 201 of the act shall be applicable
to such terms when used in this part and in Parts 211
B. Subpart B - Organization & Personnel
Responsibilities of quality control unit.
Personnel Qualifications.
Personnel responsibilities.
Consultants.
C. Subpart C - Building & Facilities
Design and construction features.
Lighting.
Ventilation, air filtration, air heating and cooling.
Plumbing.
Sewage and refuse.
Washing and toilet facilities.
Sanitation.
Maintenance
D. Subpart D – Equipment
Equipment design,size, and location.
Equipment construction.
Equipment cleaning and maintenance.
Automatic, mechanical, and electronic equipment.
Filters.
E. Subpart E - Control of Components & Drug Product Containers & Closures
General requirements.
Receipt and 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.
F. Subpart F - Production & Process Control

3. 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.
G. Subpart G - Packaging & Labeling Control
Materials examination and usage criteria.
Labeling issuance.
Packaging and labeling operations.
Tamper-resistant packaging requirements for over-the-counterhuman drug products.
Drug product inspection.
Expiration dating.
H. Subpart H - Handling & Distribution
Warehousing procedures.
Distribution procedures.
I. Subpart I - Laboratory Control
General requirements.
Testing and release for distribution.
Stability testing.
Special testing requirements.
Reserve samples.
Laboratory animals.
Penicillin contaminat
J. Subpart J - Records & Reports
General requirements.
Equipment cleaning and use log.
Component, drug product container, closure, and labeling records .
Masterproduction and control records.
Batch production and control records.
Production record review.
Laboratory records.
Distribution records.
Complaint files.
K. Subpart K - Returned & Salvaged Drugs
Returned drug products.
Drug product salvaging.