Clean Room Validation

When a cleanroom has been built and is about to be handed over to the purchaser, or when a cleanroom is reopened after being shut down for modifications that could changes to its contamination control characteristics, it will be validated. This initial type of testing (validation) is to establish that the cleanroom is working correctly and achieving the contamination standard that it has been designed to fulfill.

These standards are laid down in ISO 14644-1 with the methods used to test a cleanroom being given in ISO 14644-3.

A Secondary function of this initial testing is to establish the initial performance of the room so that this can be adopted for benchmark. When the room is checked in future, and a contamination problem is encountered, deviation from the initial conditions may be found, and the possible reason for contamination thus ascertained.

Cleanroom Validation is done to

a) To ensure that new room performs as per designed.

b) To ensure that the room continues to perform as per designed.

We Specialized In Clean-Room & Operation Theater Validation For ISO & NABH Licensed Facilities And Offer A Complete Range Of Performance Tests Including:

• Air Velocity Test & Air Change Per Hour
• Non-Viable Airborne Particulate Monitoring
• HEPA Filter Integrity Testing
• Clean-Up Recovery Test
• Air Flow Pattern Test.