QPharma got its start as a validation services company in 1994.  Today, the delivery of top-quality validation solutions continues to be a core focus of our Professional Services consulting division, which serves the pharmaceutical, medical device, biotech, animal health, cosmetic, and tissue industries.

QPharma’s Validation Solutions group strives daily to provide superior service and support in a consistent, cost-effective manner. Our ongoing investments in training, research, and technology ensure that our colleagues remain at the top of the industry, and we remain resolutely committed to living up to our reputation for excellence.  From small projects to major, long-term remediation engagements, QPharma stands behind each and every solution we deliver — and our wide range of specialties enables us to serve as an end-to-end regulatory compliance partner to our valued clients.

Areas of Specialty

  • Computer System Validation
  • Process Validation
  • Equipment Qualification
  • Cleaning Validation
  • IT Infrastructure Qualification
  • Facility/Utility Commissioning and Qualification
  • Analytical and Microbiological Methods Validation

Specific Service Offerings

  • Validation Program Development
  • Validation Planning
  • Vendor Auditing
  • Risk Assessment and Mitigation
  • User Requirements Gathering and Documentation
  • System Design Documentation (FRS, DS)
  • Qualification Protocol (IQ, OQ, PQ) Development
  • Qualification Protocol Execution
  • Validation Reporting
  • Traceability Matrices
  • SOP Development and Review
  • Validation Project Management
  • Validation Gap Analysis and Remediation

To learn more about QPharma’s leading reputation as a validation services provider, please contact us.