Test for the content of microbial contaminants in compressed air for pharmaceuticals.

Measurement of microbial contamination substances in compressed air supporting the manufacture of sterile pharmaceuticals.

In the pharmaceutical industry, strict sterility of the manufacturing environment is required to ensure product quality and safety. In particular, compressed air can come into direct contact with the product during the manufacturing process, making it important to manage the risk of microbial contamination. Our testing of microbial contamination levels in compressed air evaluates microorganisms in the compressed air using the SA sampler from VWR, which has a proven track record in GMP pharmaceutical factories. Designed for use in clean rooms, it is ideal for assessments in environments that require high cleanliness. It also contributes to the establishment of new compressed air and gas systems, as well as regular microbial contamination evaluations and identification of contamination sources. 【Usage Scenarios】 - Quality control of compressed air in the aseptic pharmaceutical manufacturing process - Regular microbial monitoring of compressed air systems in clean rooms - Investigation of contamination sources when microbial contamination from compressed air is suspected 【Benefits of Implementation】 - Reduction of microbial contamination risks in aseptic pharmaceutical manufacturing - Improvement of product quality and safety - Increased reliability of the manufacturing process

Other contract services