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Domestic standard specification of clean workshop_Industry News_News_sz-pharma

by:PHARMA     2022-09-23
Clean pharmaceutical cleanroom refers to the removal of particulates, harmful air, bacteria and other pollutants in the air within a certain space, and control of indoor temperature, cleanliness, indoor pressure, airflow velocity and airflow distribution, noise and vibration, lighting, and static electricity. A specially designed room within a certain range of needs. Shanghai Leijian Building Decoration Engineering Co., Ltd. is a professional and technical company engaged in the research and development, production, sales and installation of purification series products. The second-level qualification for contracting, the third-level qualification for professional contracting of construction electromechanical installation engineering, the second-level qualification for professional contracting of fire protection facilities engineering, and the second-level qualification for professional contracting of electronic and intelligent engineering. The company has complete various qualification certificates, strong technical force, excellent engineering pharma machinery, and perfect testing pharma machinery. It can provide you with all the products and accessories needed to equip clean room purification air conditioners. It has a color steel plate production line. Share the domestic standards and specifications of clean workshops. 1. GB50073-20012 for the design of clean workshops, GB50333-20023 for the design of clean workshops in hospitals, GB50457-20084 for the design of clean workshops in the pharmaceutical industry, and GB50457-20084 for the design of infectious disease hospitals. /T16292-19966, QS certification quality manual 7, GMP pharmaceutical production quality management practice 8, clean room construction and acceptance specifications GB 5091-2010
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