Services

GxP Computer Validation

IT Validation Department

Setting the scene

Our IT 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:

  • Drafting work instructions (WI)
  • Drafting of standard operating procedures (SOPs)
  • Drafting of change management procedures
  • Drafting of validation summary reports (VSR)
  • On-site acceptance testing (SAT)
Let's work together to write your standards and procedures