Pharmaceutical production and packaging must be strictly controlled indoor floating particles and bacteria contamination produced 100,000 gmp purification plant, so that the cleanliness of the production environment meet the technical requirements to ensure the safety of medicines. In general, there is an air purifier: air filter, organize sewage flow to improve indoor air static pressure. Pharmaceutical production and packaging clean room environment control requirements: 高标准 purification plant environmental control requirements: that the air cleanliness workshop air cleanliness of our 高标准 clean room requirements are as follows: A, provide clean air to produce the desired level of clean indoor air of dust and microbial count should be monitored regularly and record levels of different static pressure difference between the clean room should be kept within the specified value. B, clean room temperature and relative humidity should be adapted to the requirements of its production process. C, penicillins, production areas highly sensitizing and anti-tumor drugs should be set independent air conditioning system, the exhaust should purification. Should be strictly controlled clean room air cleanliness gmp purification plant design, and environmental temperature, humidity, fresh air volume and pressure and other parameters: the level of cleanliness and ventilation A, pharmaceutical production and packaging of the number of clean room production and packaging of drugs cleanroom air cleanliness divided into 100, 10 000, 100 000, 300 000 4 levels to determine the clean room air changes, the need for the wind to compare quotes gmp purification plant, taking the maximum, in practice In gmp purification plant, 100 times the number of ventilators 300-400 / hour, 10,000 50-80 times / hour, 100 000 20-50 times / hour. B, cleanliness zoning pharmaceutical production and packaging environment cleanliness can refer to a specific partition table selection. Categories 100,000 clean room use can be divided into two categories: (1) industrial clean room - with inanimate particles as a control object. The main control particulate pollution work inanimate objects, generally maintain a positive pressure inside. It is suitable for precision industry, electronic industry, aerospace industry, nuclear industry, printing industry, the photographic industry and other sectors. (2) biological clean room - to have a life of particulate control objects, can be divided into: ① general biological clean room. The main control particulate pollution on the work life of the object. At the same time the material is subjected to a variety of internal erosion sterilizing agent, generally maintain a positive pressure inside. Can be used in the pharmaceutical industry, food industry, medical facilities, laboratory facilities. ② biosafety clean room. The main object of control of life on the outside and people particulate pollution, the need to maintain a negative pressure inside. For laboratory facilities, biological engineering, medical facilities. gmp gmp Binzhou purification plant purification plant construction _ _ preferred Ecota purification by decontamination Ltd. Shandong Yick Tak. Shandong Ecota decontamination Ltd. (www.shandongyide.cn) strong, credible, in Jinan, Shandong's construction industry has accumulated a large number of loyal customers. The company better work attitude and constantly improving innovative ideas will lead Shandong Ecota purify and you work into the brilliant, for a better future!