pharmaceutical process validation

FAQs from Inspectors About Cold Chain and Transport Controls

FAQs from Inspectors About Cold Chain and Transport Controls FAQs from Inspectors About Cold Chain and Transport Controls The pharmaceutical industry is highly regulated, and maintaining compliance throughout the product lifecycle is of utmost importance. Cold chain and transport controls…

Bridging Studies for Cold Chain Packaging Change Justification

Bridging Studies for Cold Chain Packaging Change Justification Bridging Studies for Cold Chain Packaging Change Justification The pharmaceutical industry has increasingly adopted innovative approaches to ensure product integrity throughout transport and storage. As regulatory requirements evolve, so does the emphasis…

Integration of Cold Chain Validation with Site QMS

Integration of Cold Chain Validation with Site QMS Integration of Cold Chain Validation with Site QMS In the pharmaceutical industry, ensuring product integrity throughout the cold chain is paramount. This article presents a step-by-step tutorial on the integration of cold…

Case Study: Packaging Stability Risk Identified via CPV Data

Case Study: Packaging Stability Risk Identified via CPV Data Case Study: Packaging Stability Risk Identified via CPV Data Step 1: Developing the User Requirements Specification (URS) and Conducting a Risk Assessment The initiation of a pharmaceutical process validation lifecycle begins…

Real-Time Shelf Life Assessment with New Packaging Systems

Real-Time Shelf Life Assessment with New Packaging Systems Real-Time Shelf Life Assessment with New Packaging Systems In the pharmaceutical industry, the validation of packaging systems is crucial for ensuring product stability, safety, and efficacy over their intended shelf lives. This…

Regulatory Guidelines on Packaging Stability Data Submission

Regulatory Guidelines on Packaging Stability Data Submission Regulatory Guidelines on Packaging Stability Data Submission In the pharmaceutical industry, ensuring the safety and efficacy of drug products relies heavily on robust validation processes. Among these, pharmaceutical process validation is critical to…

Frequently Asked Questions by Inspectors About HVAC Systems

Frequently Asked Questions by Inspectors About HVAC Systems Frequently Asked Questions by Inspectors About HVAC Systems Step 1: Understand User Requirements Specification (URS) and Risk Assessment The foundation of any successful validation process begins with a clear understanding of the…

Aligning HVAC Validation with ICH Q9 Risk Management Principles

Aligning HVAC Validation with ICH Q9 Risk Management Principles Aligning HVAC Validation with ICH Q9 Risk Management Principles The validation of Heating, Ventilation, and Air Conditioning (HVAC) systems in pharmaceutical manufacturing is critical for ensuring product quality and compliance with…

Examples of HVAC Failures That Led to Product Recalls

Examples of HVAC Failures That Led to Product Recalls Examples of HVAC Failures That Led to Product Recalls In the pharmaceutical industry, maintaining optimal conditions in manufacturing environments is critical to ensure product quality and compliance with regulatory standards. A…

Audit-Ready Filing of Validation Files: Best Practices

Audit-Ready Filing of Validation Files: Best Practices Audit-Ready Filing of Validation Files: Best Practices In the pharmaceutical industry, compliance with regulatory standards is essential for the safety and efficacy of drug products. Pharmaceutical process validation is a critical component that…