Tag: validation in pharmaceutical industry

When Is Requalification Required for Legacy Systems?

When Is Requalification Required for Legacy Systems? When Is Requalification Required for Legacy Systems? In the pharmaceutical industry, the validation of legacy systems often presents unique challenges and opportunities. Modern regulatory frameworks have established stringent guidelines that ensure compliance with…

Key Performance Indicators (KPIs) for CPV Tracking

Key Performance Indicators (KPIs) for CPV Tracking Key Performance Indicators (KPIs) for CPV Tracking In the pharmaceutical industry, maintaining compliance with regulatory requirements while ensuring product quality is paramount. This step-by-step guide focuses on the critical aspect of Continued Process…

Setting Up a CPV Program: Requirements and Tools

Setting Up a CPV Program: Requirements and Tools Setting Up a CPV Program: Requirements and Tools The implementation of a Continued Process Verification (CPV) program is essential for ensuring the consistent quality of pharmaceutical products throughout their lifecycle. CPV enables…

PQ vs PV: Understanding the Differences in Pharma Validation

PQ vs PV: Understanding the Differences in Pharma Validation PQ vs PV: Understanding the Differences in Pharma Validation Validation is a crucial aspect of ensuring that products manufactured in the pharmaceutical industry meet quality standards and regulatory requirements. The concepts…