Cleaning and sterilization validation programs to meet FDA requirements.
Client: Reusable Medical Devices
Date: 16 Aug, 2018
Categories: ALL
Reusable Medical Device
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A cleanroom is qualified that the conditions are suitable for manufacturing.
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.
