by Dr. Yashashwini Reddy | Jun 9, 2025
What is a Validation Master Plan (VMP)? A Validation Master Plan is a high-level document that outlines the overall strategy, scope, approach, and responsibilities for validation activities within a pharmaceutical facility. It serves as a roadmap to ensure all...
by Dr. Yashashwini Reddy | Jun 9, 2025
Importance of Validation in Pharmaceuticals Validation in the pharmaceutical industry is a documented process that proves that a system, equipment, method, or process consistently produces a result meeting predetermined quality standards. It is a fundamental part of...
by Dr. Yashashwini Reddy | Jun 9, 2025
Three Consecutive Batches for Validation in Pharmaceuticals Definition: In pharmaceutical manufacturing, validation is the documented evidence that a process consistently produces a product meeting its predetermined quality specifications. One of the critical...
by Dr. Yashashwini Reddy | May 6, 2025
A Checklist to Review Tablet Process Validation is essential for ensuring that tablet manufacturing processes are consistently producing products that meet predefined specifications and regulatory requirements. Process validation in pharmaceutical manufacturing is a...
by Dr. Yashashwini Reddy | May 2, 2025
Revalidation plays a critical role in maintaining product quality and ensuring regulatory compliance in pharmaceutical manufacturing. It is an essential component of Good Manufacturing Practices (GMP) and a requirement by regulatory authorities like the FDA, EMA, and...
