'*Drug and cosmetic Act 1940* Schedule M1 describes the good manufacturing practices and requirements of premises, plant and equipment for homoeopathic medicines Schedule M2 describes the requirements of factory premises for manufacture of cosmetics Schedule M3 describes the quality management system –for notified medical devices and in-vitro diagnostics Schedule N describes the list of minimum equipment for the efficient running of a pharmacy Schedule O describes the standard for disinfectant fluids Schedule P describes the life period of drugs Schedule P1 describes the pack size of drugs Schedule Q describes the list of dye, colour and pigments Part 1: List of dyes, colours and pigments permitted to be used in cosmetics and soaps Part 2: List of colours permitted to be used in soaps Schedule R describes the standards for condoms made of rubber latex intended for single use and other mechanical contraceptives Schedule S describes the standards for Cosmetics Standards laid down from time to time by the Bureau of Indian Standards Schedule T describes the good manufacturing practices for ayurvedic, siddha and unani medicines Schedule T describes form for record of utilization of raw material by ayurveda or siddha or unani licensed manufacturing units during the financial year Schedule U describes the particulars shown in manufacturing records of drugs Schedule X describes the list of habit forming and narcotic drugs ***Thank you friends**'
Tags: PHARMACEUTICAL JURISPRUDENCE , Drugs and cosmetic Act 1940
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