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 flow of sewage purification plant installation gmp 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, and environmental temperature, humidity, fresh air volume and pressure and other parameters: the level of cleanliness and ventilation A, pharmaceutical production and the number of drug packaging clean room production and packaging cleanroom air clean divided into 100 degrees, 10 000, 100 000, 300 000 4 levels to determine the clean room air changes, the need for the amount of wind compares maximum value gmp purification plant, in practice gmp purification plant design , 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. Characteristic index ① parallel flow lines (parallel flow lines of) the role of parallel flow lines is to ensure that dust will not be a source of dust particles emitted perpendicular to the flow direction of propagation. Parallel between the requirements of both the flow line (at 0.5m distance between the inside angle of not less than 15 °), but require as much as possible perpendicular to the air flow line side (which is not less than the minimum angle of 65 °). ② turbulence degree (speed unevenness) role is to ensure uniform speed transverse particle exchange between the minimum flow line. The degree of turbulence is to illustrate the degree of centralization or discrete velocity field defined. ③ This is to ensure that the lower wind speed cleanroom contamination control following four minimum wind speed. Self-cleaning time is cleanroom contamination reply from state to reflect the steady state capacity, the shorter the better. You can also specify to reduce pollution from one state to a clean state. Turbulence cleanroom self-purification time is generally no more than 30min. gmp purification plant construction, Shandong Ecota purification, purification plant gmp Tai'an, Shandong benefits provided by the German decontamination Limited. Shandong Ecota decontamination Ltd. (www.shandongyide.cn) is a leader in Jinan, Shandong Province, construction, over the years, the company is implementing the scientific management, innovation and development, the principle of honesty and trustworthiness, and satisfy customer needs. Shandong Ecota purification leadership with the staff warmly welcome all inquiries negotiations to create Shandong Ecota purify a better future.