Introduction to our company's purification workshop
The design of our company's clean room purification workshop is essential to ensure the quality of pharmaceutical production. In order to minimize the pollution and cross-contamination of pharmaceuticals, we will create a controlled environment for the production of pharmaceuticals to meet the requirements of its production process. Qualified medicines to ensure people's health and safety.
The Good Manufacturing Practices (GMP) stipulates that the production environment parameters in the clean factory building for pharmaceutical production are as follows: temperature and relative humidity and pressure difference are determined by the production process. The general temperature is 18 ° C ~ 24 ° C, relative The humidity is 45%~65%. It is more specific in the “Guidelines for the Implementation of Good Manufacturing Practices” (GMP). The temperature and relative humidity in the clean room of the drug production are not produced by the operator wearing the clean overalls. Comfortable and uncomfortable as the benchmark.