Commissioning Qualification Validation

Why Us

When working with ViridianTechs, you can expect a seamless, FDA and EMA compliant, customized solution to all your computer systems validation needs. With our consulting experience in the life science industry, we fully understand that computer systems are vital for a company’s success. Our specific areas of expertise within computer systems validation are included below. Developing and bringing life-changing drugs and devices to market: that’s your job. Expert computer systems validation consulting: that’s ours. You have enough to accomplish; let us be your resource for computer systems validation. As a global leader specializing in computer systems validation consulting services, ViridianTechs work to ensure life sciences companies’ processes are functional and fully compliant with FDA and EMA guidelines.

  • Utilities Equipment
  • Processes
  • Cleaning Validation
  • Test Method Validation
  • Greenfield CQV Projects​
  • New Production Suite Commissioning​
  • Decommissioning

  • Project Planning
  • User Requirements Specifications (URS)
  • Risk Assessments
  • Protocols
  • FAT
  • SAT
  • Summary Reports
  • Traceability Matrixes
  • Calibration Matrix
  • SOPs
  • Integrated Commissioning and Qualification (ICQ)
  • Validation Protocol Format
  • Design Qualification (DQ)
  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Good Automated Manufacturing Practice (GAMP)
  • Current Good Manufacturing Practice (cGMP) Review
  • Continued Process Verification (CPV)
  • Pre-Operational Verifications
  • Commissioning and Startup
  • Technical Audits and Due Diligence
  • Validation Master Plans (VMP)

What We Do

Our team of professionals supports life science companies in all aspects of the CQV lifecycle. We facilitate a timely and cost-effective solution tailored to your company’s budget and requirements.