Skip to main content

Commissioning & Qualification Validation (CQV) tracking

Understanding and validating the quality of the design, installation, operation, performance, cleanliness and process product is vital for the qualification of a new pharmaceutical plant or upgrade of an existing plant.

Using Orbit to track the full validation lifecycle provides live and up to date status reporting on progress and any issues found. Orbit can create and digitise:

  • The validation plan.
  • The design review and qualification procedure
  • The factory acceptance test(s) FAT
  • All commissioning inspections and test requirements
  • Installation Qualification procedure
  • Operations Qualification procedure (including SAT)
  • Performance Qualification procedure
  • Cleaning Qualification procedure
  • Process Validation procedure

Once in Orbit the inspection and test requirements as well as the qualification procedures can be fully executed, and status tracked within Orbit. When fully complete Orbit can produce the fully compiled validation summary report.

Want to find out more about how Orbit can improve your project?

Contact Us Today

Status and Progress

Orbit once configured and populated can interface CQV activities with work execution flow schedules (WEFS) or diagrams. Once configured and set up then milestone driven activities can be identified with full and live status reporting directly on the WEFS using data sourced directly from Orbit.

Status and Progress

Orbit at the heart of our OCCMS Services

As well as our state-of-the-art Orbit software, OCCMS also offers a wide range of services designed to achieve the best outcome for your completions, commissioning and project management delivery.