Revalidation & Change Control

Differences Between Requalification and Revalidation

Differences Between Requalification and Revalidation Differences Between Requalification and Revalidation Understanding the distinctions between requalification and revalidation is critical for maintaining compliance with regulatory standards in the pharmaceutical industry. This article outlines a structured approach to process validation in pharma,…

When to Perform Full vs Partial Revalidation

When to Perform Full vs Partial Revalidation When to Perform Full vs Partial Revalidation In the pharmaceutical and biologics industries, the integrity of manufacturing processes is paramount. As part of the validation lifecycle, understanding when to perform full versus partial…

How to Document Revalidation Justifications in QA Systems

How to Document Revalidation Justifications in QA Systems How to Document Revalidation Justifications in QA Systems The validation lifecycle in the pharmaceutical industry is a critical process that ensures product quality and compliance with regulatory requirements. This article serves as…

Revalidation SOP Template: Periodic, Planned & Emergency Changes

Revalidation SOP Template: Periodic, Planned & Emergency Changes Revalidation SOP Template: Periodic, Planned & Emergency Changes In the pharmaceutical industry, the importance of revalidation cannot be overstated. Revalidation ensures that processes remain in a state of control, fulfilling regulatory requirements…

Cleaning Revalidation: When Is It Required?

Cleaning Revalidation: When Is It Required? Cleaning Revalidation: When Is It Required? In pharmaceutical and biologics manufacturing, cleaning validation is a critical component to ensure that equipment used in production is maintained in a state of cleanliness that prevents cross-contamination…

Regulatory Expectations for Periodic Revalidation Frequencies

Regulatory Expectations for Periodic Revalidation Frequencies Regulatory Expectations for Periodic Revalidation Frequencies In the pharmaceutical industry, maintaining compliance with regulatory expectations is crucial for ensuring product quality and safety. Periodic revalidation plays a significant role in lifecycle management, ensuring processes…

Process vs Equipment Revalidation: Scope and Depth Explained

Process vs Equipment Revalidation: Scope and Depth Explained Process vs Equipment Revalidation: Scope and Depth Explained Revalidation is a critical component of the pharmaceutical manufacturing process that ensures ongoing compliance with regulatory standards. This article provides a comprehensive, step-by-step validation…

Role of Risk Assessment in Deciding Revalidation Scope

Role of Risk Assessment in Deciding Revalidation Scope Role of Risk Assessment in Deciding Revalidation Scope The validation lifecycle of pharmaceutical products entails a meticulous approach to ensure compliance with regulatory requirements and maintain product quality. One vital aspect is…

Equipment Swapping and Its Revalidation Implications

Equipment Swapping and Its Revalidation Implications Equipment Swapping and Its Revalidation Implications In the context of pharmaceutical quality assurance, equipment revalidation is critical to ensure continued compliance with regulatory standards and to maintain the integrity of the manufacturing process. This…

Case Study: Revalidation Due to Raw Material Supplier Change

Case Study: Revalidation Due to Raw Material Supplier Change Case Study: Revalidation Due to Raw Material Supplier Change The pharmaceutical industry is governed by stringent regulations that require the validation of processes and products to ensure safety and efficacy. When…