Simplifying CPV Validation and Consistency
How to implement a consistent CPV initiative with minimal validation efforts
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:
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Achieve secure compliant manufacturing operations
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Reduce FDA onsite audit time by 50%
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Prepare APRs 90% faster
