Biotech and pharmaceutical products must be manufactured in compliance with the current Good Manufacturing Practice (cGMP) regulations. Monitoring these areas meets the requirement for environmental ...

The relevant classifications of pharmaceutical cleanrooms are grouped according to the particle concentration of the air that must conform to the cleanliness criteria for the manufacturing process ...

The United States Pharmacopeia (USP) and others, such as EP, JP, and ChP, have developed test techniques to ensure that particle counts are kept to a minimum in intravenous injections (parenteral ...