A cleanroom is qualified that the conditions are suitable for manufacturing.
Date: 17 Aug, 2018
Categories: ALL
Cleanroom Validation
We Offer Great Services to our Clients
Cleaning and sterilization validation programs to meet FDA requirements.
Methods include EO, Steam, VHP, Radiation, UV, Ozone, Pulsed-Light, Dry Heat, and Liquids.
Container Closure Integrity (CCI) of non-porous packages and breathable packages.
