Helping you to win your compliance battles

We can support you across the full validation lifecycle of your manufacturing equipment, systems and facilities. We have significant experience in the qualification of the following systems and equipment to ensure compliance with International Standards and Regulatory expectations:

    • Facility Qualification
    • Cleanroom and Associated HVAC System Qualification
    • Clean Utilities (Water & Steam)
    • Utility Gases and Compressed Air
    • Aseptic Filling Lines (Vial, Ampoule and Pre-Filled Syringe)
    • Solid Dose Manufacturing Equipment
    • Sterilisation Processes (Autoclaves, Depyrogenation, VHP & Ethylene Oxide systems and UV systems)
    • CIP/SIP
    • Visual Inspection (manual and automated processes)
    • Packaging Equipment
    • Process Validation
    • Cleaning Validation
    • Thermal Mapping

Victory Compliance Group can develop and execute the full validation lifecycle documentation for your projects, from User Requirements Specification, risk and impact assessments through to qualification protocols (DQ, IQ, OQ and PQ), Requirements Traceability Matrix development and Final Summary Reporting. We can also track and manage the closure of qualification deviations / discrepancies identified during the execution phase.