PHARMA newly gmp cleanroom check now for electronics factory

According to GMP regulations, the preparation, the fine drying package of API, the raw and auxiliary materials used in the preparation and the packaging materials directly in contact with the medicine should be produced in the clean area.

The clean room or clean zone of a pharmaceutical producing enterprise refers to the area that requires specified environmental control for dust particles and microbial pollution. The construction structure, equipment and use of the clean room can reduce the intervention, generation and retention of pollution sources in the area. Therefore, the clean room of a pharmaceutical producing enterprise has its own characteristics.

Characteristics 1.Clean room is a special designed room to exclude the particles in the air, bacteria and other harmful air pollutants 2. the indoor temperature, cleanliness, interior pressure, air velocity and air distribution, noise, vibration, and lighting, static control within the scope of a certain demand. 3. That is no matter how the outside air conditions change, its indoor all can maintain the original set requirements of cleanliness, temperature and humidity and pressure performance characteristic.