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Category: Schedule

  • Schedule T:Good manufacturing Practice for Ayurvedic, Sidha and Unani Medicines

    Schedule A B C D E F G H H1 I J K L M N O P Q R S T U V W X Y Z SCHEDULE T (See rule 157) Schedule T is defined as the schedule of drugs and cosmetic act & rules which represents the good manufacturing practice of asu (ayurvedic, siddha and unani) medicines along with area required for premises, specification required, qualification required, recommended machinery and equipment etc. GOOD MANUFACTURING PRACTICES FOR AYURVEDIC, SIDDHA AND…

  • Schedule S:Standards for Cosmetics

    Schedule A B C D E F G H H1 I J K L M N O P Q R S T U V W X Y Z Schedule S:   Schedule S describes standards for cosmetics in finished form.− The following cosmetics in finished form shall conform to the Indian Standards specifications laid down from time to time by the Bureau of Indian Standards (BIS) Skin Powders. Skin Powder for infants. Tooth Powder. Toothpaste. Skin Creams. Hair Oils. Shampoo, Soap-based. Shampoo,…

  • Schedule R and R1

    Schedule A B C D E F G H H1 I J K L M N O P Q R S T U V W X Y Z Schedule R: Schedule R describes the standards for condoms made of rubber latex intended for single use and other mechanical contraceptives I-CondomsII- Other Mechanical Contraceptive e.g. Copper T and Tubal Rings Schedule R1: Schedule R1 describes the following medical devices shall conform to the Indian Standards specifications laid down from time to time by…

  • Schedule Q:List of Dyes, Colors and Pigments used in Cosmetics and Soaps

    Schedule A B C D E F G H H1 I J K L M N O P Q R S T U V W X Y Z Schedule Q:   Schedule Q describes the list of Dyes, Colors and Pigments permitted to be used in Cosmetics and Soaps. Part 1: List of Dyes, colours and Pigments permitted to be used in Cosmetics and Soaps as given under IS : 4707 (Part I)-1988 as amended by the Bureau of Indian Standards… Part…

  • Schedule P: Life Period of Drugs

    Schedule A B C D E F G H H1 I J K L M N O P Q R S T U V W X Y Z Schedule P:   Schedule P describes the life period of drugs in months (unless otherwise specified) between date of manufacture and date of expiry which the labelled potency period of the drug shall not exceed under the conditions of storage specified in column no. 4 of schedule P. Column No. 1 defines the serial…

  • Schedule L: Omitted

    Schedule A B C D E F G H H1 I J K L M N O P Q R S T U V W X Y Z Schedule L (Omitted)    Schedule L-1: Good laboratory practices and requirements of premises and equipments General Requirements Premises Personnel Equipments Chemicals and Reagents Good house keeping and safety Maintenance, calibration, and validation of equipments Reference materials Microbiological Cultures Quality system Internal quality system audits Management review Standard Operating Procedures Protocols and specifications archive Raw…

  • Schedule O describes the standards for Disinfectant Fluids.

    Schedule A B C D E F G H H1 I J K L M N O P Q R S T U V W X Y Z Schedule O: Schedule O describes the standards for Disinfectant Fluids. Part 1 Describes the provision applicable to black fluid and white fluids that are derived from petroleum with or without hydrocarbon. Part 2: Describes provisions applicable to other disinfectant fluids not covered in part 1.