Pharmaceutical Test Chambers Designed to Meet Quality Regulations for CGMP
The pharmaceutical industry uses AES environmental test chambers extensively in product research and development, as well as in manufacturing. This industry develops, produces, and markets drugs or pharmaceuticals licensed for use as medications, as well as vaccines, blood products, and biologics. The main regulatory standard for ensuring pharmaceutical quality is the Current Good Manufacturing Practice (CGMPs) regulation for human pharmaceuticals enforced by the US Food and Drug Administration (FDA). These regulations enforce establishing strong quality management systems and maintaining reliable testing laboratories. Veterinary pharmaceutical companies are also regulated by the FDA. AES designs, manufactures, installs, and supports standard and customized environmental test chambers for testing high/low temperatures and humidity variations in the pharmaceutical industry.