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CQV Pharma Services

For over 30 years, PV (Performance Validation) has provided comprehensive CQV services across the nation for the life science industry. With projects ranging from small system qualifications to multi-million-dollar greenfield manufacturing facilities, PV has a proven track record to manage every phase of the CQV life cycle. Our team of experts works with our client’s standard operating procedures (SOPs) and leverages Good Manufacturing Practices (GMP) to deliver the proper documentation to release quality and safe products to the market.

PV serves the following areas:
Pharma, Biotech, CDMO, CMO, Animal Health, IVD manufacturing, Key industry suppliers

PV provides the documented evidence our clients need to ensure that systems are installed and properly functioning according to their intended use, so our client’s facility consistently produces quality and safe products. 

Types of Services:
Quality Risk Management (QRM) I Commissioning and Qualification (C&Q) I
Process Validation Corrective Action/Preventive Action (CAPA) I
Preventive Maintenance Calibration I Automation/Continuous Monitoring I
Change Control I Training

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Brad Henry

Vice President, Indiana Division Director - Brad has over 20 years of experience managing and executing CQV projects for the pharmaceutical and medical device industries. He has extensive experience in dry products, parenteral, facilities and utilities, and in-vitro diagnostics.

Schedule with Brad Henry

John Underwood

Vice President, Michigan Division Director - With over 20 years of industry experience, John has been fortunate enough to experience all levels at PV and has provided services to the pharmaceutical and medical device manufacturing industries. He has extensive experience in dry products, parenteral, facilities and utilities, API, and computer systems.

Schedule with John Underwood