Tag: Stage 3

Using CPV Outcomes to Trigger Revalidation or Tech Transfers

Using CPV Outcomes to Trigger Revalidation or Tech Transfers Using CPV Outcomes to Trigger Revalidation or Tech Transfers Step 1: Understanding the Basics of Sterilisation Validation Sterilisation validation is a crucial aspect of the pharmaceutical manufacturing process, ensuring that products…

CPV Template and Checklist for QA Teams

CPV Template and Checklist for QA Teams CPV Template and Checklist for QA Teams Continued Process Verification (CPV) is a critical component of process validation within the pharmaceutical industry. Emphasized by regulatory guidelines such as the FDA Process Validation Guidance…

How to Present CPV Data During Regulatory Audits

How to Present CPV Data During Regulatory Audits How to Present CPV Data During Regulatory Audits In the current regulatory landscape, the pharmaceutical industry faces stringent scrutiny regarding the implementation and effectiveness of Continued Process Verification (CPV) programs. This article…

CPV and OOS/OOT Events: Investigation Flow and Records

CPV and OOS/OOT Events: Investigation Flow and Records CPV and OOS/OOT Events: Investigation Flow and Records In the pharmaceutical industry, Continued Process Verification (CPV) and the effective management of Out of Specification (OOS) and Out of Trend (OOT) events are…

Building Dashboards for CPV Visualization (Excel + Power BI)

Building Dashboards for CPV Visualization (Excel + Power BI) Building Dashboards for CPV Visualization (Excel + Power BI) Continued Process Verification (CPV) is a critical aspect of process validation that ensures that processes remain in a state of control throughout…

Handling Process Variability Identified in CPV

Handling Process Variability Identified in CPV Handling Process Variability Identified in CPV Step 1: Understanding the Role of Continued Process Verification (CPV) Continued Process Verification (CPV) is an essential aspect of process validation, ensuring that a manufacturing process remains in…

How to Trend Process Parameters Across Lots for CPV

How to Trend Process Parameters Across Lots for CPV How to Trend Process Parameters Across Lots for CPV Continued Process Verification (CPV) is an essential component of the pharmaceutical validation lifecycle that ensures processes remain in a state of control…

Role of LIMS and QMS in CPV Automation

Role of LIMS and QMS in CPV Automation Role of LIMS and QMS in CPV Automation In the pharmaceutical and biologics sectors, compliance with strict regulatory standards is crucial for quality assurance and product integrity. Continued Process Verification (CPV) plays…

Linking CPV to Product Quality Complaints and Deviations

Linking CPV to Product Quality Complaints and Deviations Linking CPV to Product Quality Complaints and Deviations Continued Process Verification (CPV) is integral to ensuring consistent product quality throughout the product lifecycle. This tutorial provides a comprehensive, step-by-step guide on how…

CPV Review Frequency: Monthly, Quarterly, or Annually?

CPV Review Frequency: Monthly, Quarterly, or Annually? CPV Review Frequency: Monthly, Quarterly, or Annually? Continued Process Verification (CPV) is an essential component of a robust pharmaceutical validation strategy, ensuring the consistent quality of products in line with FDA Process Validation…