Documentation – EU GMP
EU GMP Guidelines for Documentation | EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use |
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Premises and Equipment – EU GMP
EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use | EU GMP Guidelines for Premises and Equipment |
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Personnel – EU GMP
EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use | EU GMP Guidelines for Personnel |
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Pharmaceutical Quality System – EU GMP
EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use
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SCHEDULE M-II
Good Manufacturing Practices and Requirements of Premises, Plant and Equipment for Cosmetics
SCHEDUE M-I
Good Manufacturing Practices and Requirements of Premises, Plant and Equipment for Homoeopathic Medicines
SCHEDULE M – GMP – PART 7 (API-BULK DRUGS)
GOOD MANUFACTURING PRACTICES FOR ACTIVE PHARMACEUTIAL INGREDIENTS-API (BULK DRUGS)
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SCHEDULE M – GMP – PART 6 (METERED-DOSE-INHALERS)
GOOD MANUFACTURING PRACTICES FOR METERED-DOSE-INHALERS (MDI)
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SCHEDULE M – GMP – PART 5 (TOPICAL PRODUCTS)
GOOD MANUFACTURING PRACTICES FOR TOPICAL PRODUCTS i.e. EXTERNAL PREPARATIONS (CREAMS, OINTMENTS, PASTES, MULSIONS, LOTIONS, SOLUTIONS, DUSTING POWDERS AND IDENTICAL PRODUCTS)
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