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Pharmaceutical Equipment Validation (PEV) is a UK-based independent service provider specializing in the validation and testing of equipment, facilities, and utilities for the pharmaceutical, biotech, and medical research industries. The company is recognized for its expertise in thermal sterilization testing and consultancy. Its reports have passed audits from major regulatory bodies such as the FDA, MHRA, BSI, as well as client quality systems. Services include protocol development for Factory Acceptance Tests (FATs), Site Acceptance Tests (SATs), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Requalification (RQ), autoclave testing, auditing of reports, and more. The company operates with GMP-trained engineers using calibrated test equipment to ensure compliance with Good Manufacturing Practices.
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