GxP Computer System Validation

Service Validation informatique


Our Computer Validation Specialists (VSI/CSV), Quality Assurance Managers and Quality Control Specialists are able to set up the processes and documentation required by GxP regulations, as used in the pharmaceutical industry.

Our experts can help you:

  • Writing of work instructions (WI)
  • Writing of standard operating procedures (SOP)
  • Writing of change management procedures
  • Writing of validation summary reports (VSR)
  • Execution of site acceptance test plan (SAT)
Let’s validate your standards AND procedures together