Tag: validation assay

Validation Cycle Time: Baselines, Targets, and Trends

Validation Cycle Time: Baselines, Targets, and Trends Validation Cycle Time: Baselines, Targets, and Trends The validation cycle is a critical element in the pharmaceutical industry, governing the accuracy and reliability of processes that ensure product safety and efficacy. This article…

QA Oversight in Reviewing CPV Strategy Across Lifecycle

QA Oversight in Reviewing CPV Strategy Across Lifecycle QA Oversight in Reviewing CPV Strategy Across Lifecycle In the ever-evolving landscape of pharmaceutical manufacturing, Continued Process Verification (CPV) serves as a key element in ensuring consistent product quality and compliance with…

Regulatory Expectations for Media Fill Program Robustness

Regulatory Expectations for Media Fill Program Robustness Regulatory Expectations for Media Fill Program Robustness In the pharmaceutical industry, particularly in the development and manufacturing of sterile products, ensuring the aseptic process’s integrity is crucial. This comprehensive guide will focus on…

What Happens if You Skip a Required Revalidation?

What Happens if You Skip a Required Revalidation? What Happens if You Skip a Required Revalidation? In the pharmaceutical industry, compliance with regulatory guidelines is paramount for ensuring product quality and patient safety. A key aspect of maintaining this compliance…

Real-World Deviations Traced Back Through FTA Models

Real-World Deviations Traced Back Through FTA Models Real-World Deviations Traced Back Through FTA Models In the pharmaceutical industry, ensuring consistent quality of products is paramount. Understanding the complexities of validation processes, especially within the context of deviations, is critical. This…

How to Document Linearity and Specificity Results for Audits

How to Document Linearity and Specificity Results for Audits How to Document Linearity and Specificity Results for Audits In the pharmaceutical industry, the validation of analytical methods is a critical component to ensure compliance with regulatory standards such as FDA,…

HVAC Validation for Grade A/B Cleanrooms: EU GMP Expectations

HVAC Validation for Grade A/B Cleanrooms: EU GMP Expectations HVAC Validation for Grade A/B Cleanrooms: EU GMP Expectations In the highly regulated pharmaceutical environment, validation of HVAC systems for Grade A/B cleanrooms is essential to ensure product quality and compliance…

Cleaning Validation vs Holding Time: Key Differences and Intersections

Cleaning Validation vs Holding Time: Key Differences and Intersections Cleaning Validation vs Holding Time: Key Differences and Intersections Cleaning validation and holding time validation are two critical components of the pharmaceutical validation lifecycle. Understanding the interplay between these two aspects…