Continued Process Verification (CPV)

CPV Planning in the Validation Master Plan (VMP)

CPV Planning in the Validation Master Plan (VMP) CPV Planning in the Validation Master Plan (VMP) Continued Process Verification (CPV) is a key component in the lifecycle management of pharmaceutical processes, ensuring that processes remain in a state of control…

Building a CPV Matrix by Product, Process, and Equipment

Building a CPV Matrix by Product, Process, and Equipment Building a CPV Matrix by Product, Process, and Equipment In the pharmaceutical industry, Continued Process Verification (CPV) is critical for ensuring the ongoing quality and integrity of products throughout their lifecycle.…

How to Define Sampling Frequency in CPV Lifecycle

How to Define Sampling Frequency in CPV Lifecycle How to Define Sampling Frequency in CPV Lifecycle Continued Process Verification (CPV) is an essential aspect of the pharmaceutical manufacturing lifecycle, ensuring that processes remain in a state of control after the…

Case Study: CPV Detects Process Drift Before Batch Failure

Case Study: CPV Detects Process Drift Before Batch Failure Case Study: CPV Detects Process Drift Before Batch Failure In the biopharmaceutical industry, maintaining product quality and ensuring systemic consistency throughout the manufacturing process is paramount. Continued Process Verification (CPV) is…

Ongoing Verification of Critical Process Parameters (CPPs)

Ongoing Verification of Critical Process Parameters (CPPs) Ongoing Verification of Critical Process Parameters (CPPs) The ongoing verification of Critical Process Parameters (CPPs) is an essential aspect of ensuring product quality and compliance within the pharmaceutical industry. This article serves as…

Developing a Risk-Based CPV Sampling Plan

Developing a Risk-Based CPV Sampling Plan Developing a Risk-Based CPV Sampling Plan In the pharmaceutical landscape, ensuring product quality is non-negotiable. With rigorous regulatory requirements, a robust sampling plan is essential during the Continued Process Verification (CPV) phase of the…

Aligning CPV with ICH Q8, Q9, and Q10 Guidelines

Aligning CPV with ICH Q8, Q9, and Q10 Guidelines Aligning CPV with ICH Q8, Q9, and Q10 Guidelines Pharmaceutical validation is a critical component for ensuring product quality and compliance with regulatory standards. The integration of Continued Process Verification (CPV)…

CPV During Tech Transfer and Site Change

CPV During Tech Transfer and Site Change CPV During Tech Transfer and Site Change This comprehensive guide aims to equip pharmaceutical professionals with a structured approach to Continued Process Verification (CPV) during tech transfer and site changes, ensuring adherence to…

Role of CPV in Post-Approval Change Management

Role of CPV in Post-Approval Change Management Role of CPV in Post-Approval Change Management This article serves as a comprehensive step-by-step tutorial on the role of Continued Process Verification (CPV) in post-approval change management within the pharmaceutical industry. Focusing on…

Incorporating Feedback Loops from CPV to Process Design

Incorporating Feedback Loops from CPV to Process Design Incorporating Feedback Loops from CPV to Process Design In the pharmaceutical industry, the integration of Continued Process Verification (CPV) into the product and process validation lifecycle is paramount for ensuring product quality…