Principles of Cleanroom Validation
The pharmaceutical industry is subject to heavy government regulation, and pharmaceutical cleanrooms must meet stringent standards and requirements. Cleanroom validation is performed to ensure that the:
design of the facility is fit for its intended purpose
facility, equipment, and environment meet User Requirement Specifications (URS)
facility, equipment, and environment meet defined regulatory requirements
facility, equipment, and its environment function together as a system to meet defined standards.
Our cleanroom validation process include the following six phases:
Design Qualification
Installation Qualification
Operation Qualification
Performance Qualification
Cleanroom Certification
Monitor and Control
Cleanroom Validation Classification
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