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Set requirements: sterile room, microbes, culture, colony count, temporary storage and supporting space purification level for the million level, a more, particle room, the price room, buffer room purification level of 100,000, The rest of the room without purification level. 2, clean laboratory decoration works, clean air conditioning works, electrical engineering design and installation. Area of the laboratory structure, clean decoration, clean air conditioning and automatic control system, power supply lighting, weak system.
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Biopharmaceuticals require GMP to ensure the establishment of a scientific, rigorous sterile drug production environment, process, operation and management system that minimizes all possible, potentially bioactive, dusty, pyrogenic contamination, producing high Quality, health and safety of pharmaceutical products. What we call the biopharmaceutical purification project - GMP clean plant engineering solutions and pollution control technology is to ensure the successful implementation of GMP one of the main means;
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First, the medical device purification engineering design reference:
1, the international standard \"ISO / DIS 14644\"
2, clean room plant design specifications \"GB50073-2001\"
3, medical equipment packa...
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According to the national \"Food Production Safety Law\" and \"bottled drinking water\" in the provisions of pure water production must be clean and clean workshop production plant to complete the production of cleanliness requirements in the 100,000 level, the focus of pure water production in microbes Pollution control is strict.
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