Controlling contamination through an effective monitoring programme
"Contamination within a cleanroom is caused by the non-intentional or accidental introduction of viable or non-viable particulates. Whether organisations’ primary concern is controlling micro-organisms for regulatory and safety requirements, or physical contamination for yield and quality control reasons, third-party validation testing is employed to provide certification of a cleanroom’s performance for regulatory purposes.
"In this whitepaper, I explain how in-house testing as part of a defined monitoring programme, will give greater visibility on a cleanroom’s performance."
John Merrill | Aftersales & Validation Lead at Connect 2 Cleanrooms
Talk to the experts at Connect 2 Cleanrooms about cleanroom validation
With a tailored cleanroom qualification testing schedule, Connect 2 Cleanrooms will certify the class or grade of your cleanroom facilities and localised clean air devices.
How Cleanroom Design Impacts Process Flow
Read the whitepaper on the importance of considering process flow for your cleanroom at the design s...Read more
ISO 14644-1:2015 Compliant Cleanroom Monitoring
ISO 14644-1 specifies the classification of air cleanliness in terms of the concentration of airborn...Read more
Decentralised Air Handling for Cleanrooms
Read the whitepaper on why we typically favour a decentralised approach to air handling over a centr...Read more