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  • Good Manufacturing Practices

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    Vidya Vijayan
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    GMP is part of quality assurance and comes under Schedule M regulations. It establishes general requirements for pharmaceutical manufacturing facilities and operations, including the location and surroundings of the building, water supply, waste disposal, storage areas, production areas, quality control, raw materials, equipment, worker health and sanitation, documentation, and quality assurance.

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    GMP is part of quality assurance and comes under Schedule M regulations. It establishes general requirements for pharmaceutical manufacturing facilities and operations, including the location and surroundings of the building, water supply, waste disposal, storage areas, production areas, quality control, raw materials, equipment, worker health and sanitation, documentation, and quality assurance.

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    101 views1 page

    Good Manufacturing Practices

    Uploaded by

    Vidya Vijayan
    GMP is part of quality assurance and comes under Schedule M regulations. It establishes general requirements for pharmaceutical manufacturing facilities and operations, including the location and surroundings of the building, water supply, waste disposal, storage areas, production areas, quality control, raw materials, equipment, worker health and sanitation, documentation, and quality assurance.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOCX, PDF, TXT or read online from Scribd
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    GOOD MANUFACTURING PRACTICES

    Gmp IS A PART OF QA. IT COMES UNDER SHEDULE M


    General requriments
    Location and surrounding Building and premises Water supply Disposal of waste Wearhousing area Ancillary area Production area Quality control area Raw material Label and printing material Equipment Health and sanitation of workers Documentation Quality assurance area

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