US Validation Services LLC provides FDA-regulated industries such as the Pharmaceutical, Biotechnology, and Medical Device, with validation services which will satisfy the stringent demands of current Good Manufacturing Practice (cGMP) Regulations and Quality Systems Regulations (QSR).

We can support your efforts allowing you to complete your project on-time and on-budget, while assuring compliance with the current industry regulations and standards.

Validation Services We Offer

• Equipment Validation
• Utility systems Validation
• Facility Qualification
• CFR 21, Part 11 Electronic Signatures, Electronic Records Consulting
• Validation Master Plan Development
• Validation Program and Project Management
• Calibration Program Auditing, Development and Optimization
• Computerized Systems and Software Qualification

For Details visit our Validation Services page.