Tag: media fill test usp 797

Common KPI Pitfalls in Validation Monitoring

Common KPI Pitfalls in Validation Monitoring Common KPI Pitfalls in Validation Monitoring In the pharmaceutical industry, effective validation monitoring is paramount to ensure product quality and compliance with regulatory standards. This article provides a step-by-step tutorial on the validation lifecycle…

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…

Media Fill Training Batches: Requirements and Best Practices

Media Fill Training Batches: Requirements and Best Practices Media Fill Training Batches: Requirements and Best Practices Media fill tests are pivotal in ensuring the sterility of pharmaceutical products and validating aseptic processes. These tests simulate the manufacturing process to assess…

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…

FMEA for Computer System Validation (CSV) Projects

FMEA for Computer System Validation (CSV) Projects FMEA for Computer System Validation (CSV) Projects: A Step-by-Step Guide Step 1: Understanding the URS and Risk Assessment Before embarking on any validation lifecycle, it is crucial to define clear User Requirements Specifications…

Validation of Assay Methods: Accuracy and Precision Templates

Validation of Assay Methods: Accuracy and Precision Templates Validation of Assay Methods: Accuracy and Precision Templates Step 1: User Requirements Specification (URS) & Risk Assessment The validation lifecycle begins with the User Requirements Specification (URS), which serves as the foundation…

Using Data Loggers and BMS in HVAC Validation

Using Data Loggers and BMS in HVAC Validation Using Data Loggers and BMS in HVAC Validation In the highly regulated pharmaceutical industry, ensuring the integrity of the environment where products are manufactured is paramount. HVAC (Heating, Ventilation, and Air Conditioning)…