Tag: CPV Data Collection & Trending

Setting Statistical Action and Alert Limits in CPV

Setting Statistical Action and Alert Limits in CPV Setting Statistical Action and Alert Limits in CPV Continued Process Verification (CPV) is an essential component of the pharmaceutical validation lifecycle, intended to ensure that processes remain in a state of control…

Real-Time Data Collection for Batch-to-Batch Consistency

Real-Time Data Collection for Batch-to-Batch Consistency Real-Time Data Collection for Batch-to-Batch Consistency Continued Process Verification (CPV) is essential in ensuring product quality and compliance in the pharmaceutical industry. Among its key elements is cleaning validation, which is critical to avoiding…

CPV Data Sources: MES, LIMS, BMRs, and Manual Logs

CPV Data Sources: MES, LIMS, BMRs, and Manual Logs CPV Data Sources: MES, LIMS, BMRs, and Manual Logs Continued Process Verification (CPV) has become an essential part of the pharmaceutical manufacturing lifecycle, allowing companies to ensure that their processes remain…

How to Perform Trend Analysis in CPV Programs

How to Perform Trend Analysis in CPV Programs How to Perform Trend Analysis in CPV Programs Continued Process Verification (CPV) is a critical component of the lifecycle management of a pharmaceutical product, ensuring consistency and quality throughout its commercial lifecycle.…

Establishing Control Charts and Process Capability (Cp, Cpk)

Establishing Control Charts and Process Capability (Cp, Cpk) Establishing Control Charts and Process Capability (Cp, Cpk) In the pharmaceutical and biologics industries, demonstrating control over manufacturing processes is critical for ensuring product quality and compliance with regulatory expectations. One effective…

What Data to Monitor in CPV: CPPs, CQAs, and Beyond

What Data to Monitor in CPV: CPPs, CQAs, and Beyond What Data to Monitor in CPV: CPPs, CQAs, and Beyond In the pharmaceutical and biopharmaceutical industries, Continued Process Verification (CPV) has emerged as a critical component of the overall validation…