gmp purification plant engineering, Shandong Ecota purification, Qiannan gmp purification plant provided by the German decontamination Ltd. Shandong benefits. Shandong Ecota decontamination Ltd. (www.shandongyide.cn) is specialized in "all kinds of operating rooms, pharmaceutical 高标准 workshop, P-class laboratory, GLP laboratories, electronic meter" of the enterprise, the company of "honesty, hard service "concept, to provide you with the highest quality products and services. Welcome to inquire! Contact: room manager. Pharmaceutical production and packaging must be strictly controlled indoor floating particles and bacterial contamination on production, 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 one thousand gmp flow of sewage purification plant, 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 100,000 gmp purification plant, 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 ventilation frequency gmp purification plant installation, you need to compare against the wind, taking the maximum gmp purification plant, in practice , 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. Compare a selection of air conditioning solutions, modular air handling units + chiller + HEPA This is one of the most traditional design of air conditioning system. Modular air handling units section contains various functions, such as mixing section, the early effect filter section, cooling section, secondary air segment (or intermediate), the heating section, humidification, in effect filter section, fan section and so on. Advantages:. A good air treatment effect, due to air through centralized processing, in the process of being lower air pollution levels. Air temperature, humidity control more accurate; Disadvantages: A need for supporting the freezing room or outdoor space heat pump placement.