Proper CPV (Continued Process Verification) is a crucial initiative for any biotech or biopharma company to comply with regulatory authorities, monitor processes and maintain a consistent state of control while improving manufacturing productivity.

Adopting an enterprise-wide initiative for CPV ensures consistency across different manufacturing sites while trusting that every data retrieval and contextualization process is validated and does not necessarily mean the introduction of a large additional burden to the organization.

Read this use case about a global pharmaceutical company who leveraged the BIOVIA validation-ready solution and validation best practices, while going live significantly faster and simplifying CPV adoption. Maintaining a uniform standard of data in their manufacturing analytics helped:

• Achieve secure compliant manufacturing operations
• Reduce FDA onsite audit time by 50%
• Prepare APRs 90% faster