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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.
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.
Hak Cipta:
Attribution Non-Commercial (BY-NC)
Format Tersedia
Unduh sebagai DOCX, PDF, TXT atau baca online dari Scribd
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