Pharmaceutical plant clean-Engineering Pharmaceutical plant clean room technology is the key to control the dust and microorganisms, as pollutants, microorganisms pharmaceutical factory clean room environment control a top priority. 高标准 need air purification technology, and air purification technology does not mean 高标准! Cleanliness level does not apply to the physical characterization of airborne particles, chemical, radiological and life of. Not familiar with pharmaceutical production processes and procedures, do not understand the source of contamination and pollutants accumulate in place, do not have to clear the pollutant methods and evaluation criteria that meet the requirements of the cleanliness of the clean room can produce high-quality drugs are 高标准 know on a big misunderstanding. 高标准 pharmaceutical plant transformation cleanroom prevalence of the following two conditions: (a) precisely because of the existence of errors of subjective understanding, clean technology in pollution control process adversely, culminating in some pharmaceutical companies invested heavily in transformation, drug quality has not improved significantly. Medicine cleaner production plant design, construction, equipment and facilities of the plant manufacturing, installation, production execution, and this will adversely affect the quality of products with the raw materials, packaging materials, quality, human net was net facility control program. Affect the quality of the construction aspect of the clean room because part of the process control problems, leaving hidden dangers in the installation and construction process, the following specific performance: ① air conditioning system does not clean the inner wall of the duct, the connection is not tight, leakage rate is too large; ② color plate envelope imprecise, improper clean room and technical dissection (ceiling) of the sealing measures, closed doors not closed; ③ decorative profiles and process lines in clean room to form a corner, dust; ④ individual position is not in accordance with the design requirements of the construction unable to meet the relevant requirements set out; ⑤ sealant used low quality, easy to fall off, deterioration; ⑥ return, exhaust color plate lined interlinked, to get back into the dust from the exhaust duct; ⑦ process purified water, injection water, such as stainless steel sanitary the inner wall of the pipe welding seam unformed; ⑧ duct valve action failure, intrusion of air pollution; ⑨ drainage system installation quality, but off, pipe racks, dust easily annex; ⑩ cleanroom pressure tuning failed, failed meet the production process. So, for every professional installation of the company, clean room clean room construction, whether high or low cleanliness, must prepare the project sources into the top part of the process is controlled to pharmaceutical companies. (Ii) Most of the pharmaceutical cleanroom energy saving effect is poor, an unnecessary expenditure, increased production costs of drugs. For example, some pharmaceutical purification plant in the empty state or a static test cleanliness, barely qualified, under the dynamic test (production) condition, cleanliness is not ideal; so had the air conditioning unit is set to Max Frequency conditions, so interior cleanliness to meet the requirements. Increase the number of ventilators is bound to lead to increased energy consumption, an unnecessary expenditure, increased production costs of drugs. Some pharmaceutical companies to invest savings artificial conditions arbitrarily reduce the initial investment and the design requirements, the purchase price is relatively inexpensive equipment such as chillers, pumps, fans and drug machine, these seemingly cheap low equipment efficiency, quietly put the energy consumed in vain make investors more harm than good.