Validation is an important process to ensure cleanrooms meet specific standards to be classified according to the International Standards Organization (ISO). ISO classifications ensure the integrity of the products, ranging from pharmaceuticals to semiconductors, contained in the cleanroom.
The validation process requires inspection and testing with laboratory organizations performing ongoing monitoring to demonstrate continued compliance with standards. A comprehensive cleanroom monitoring strategy that combines data acquisition, analysis and reporting will support validation, ongoing compliance efforts, and protects valuable scientific work.
Download this whitepaper to learn more about:
- Where cleanroom testing falls short
- A comprehensive monitoring solution
- Critical parameters for validation and monitoring
