Transcription of SCHEDULE M - Central Drugs Standard Control Organization
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SCHEDULE M - Central Drugs Standard Control Organization
[ SCHEDULE M]. [See Rules 71, 74, 76 and 78]. good manufacturing practices AND requirements OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS. Note: - To achieve the objectives listed below, each licensee shall evolve appropriate methodology, systems and procedures which shall be documented and maintained for inspection and reference; and the manufacturing premises shall be used exclusively for production of Drugs and no other manufacturing activity shall be undertaken therein. PART 1. good manufacturing practices FOR PREMISES AND MATERIALS.
[SCHEDULE M] [See Rules 71, 74, 76 and 78] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS. Note: - To achieve the objectives listed below, each licensee shall evolve appropriate
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GOOD MANUFACTURING PRACTICES AND, Good manufacturing practices and requirements of, Certified Pharmaceutical Good Manufacturing Practices, Certified Pharmaceutical Good Manufacturing, Annexure-1 GMP CHECKLIST, Good Manufacturing Practices, Good Agricultural and Manufacturing (Handling) Safety, Practices, Good Agricultural Practices