Every successful Pharmaceutical Validation project requires robust documentation. If a validation process is not documented, it cannot be proven to have been performed.

Our CSV services are comprehensive business offerings driven by:

  • End-to-end knowledge of pharmaceutical business and operational processes
  • Pragmatic and risk-free approach
  • GAP Assessment services for existing system
  • Use of stringent norms, processes, checklists and procedures

We ensure reliability, integrity, continuous availability of regulated business data and patient safety while enabling a quality-compliant production environment.

Our validation services follow all complaint guidelines including 21 CFR part 11, EU annex 11, GAMP 5, GDP and cGMP, and are supported by our rich domain experience in Integration of SCADA/ MES/ OPC/ LIMS etc.