by Dr. Yashashwini Reddy | Aug 9, 2025
Improving Quality Through Supplier Audits in Pharmaceuticals 1. Introduction In the pharmaceutical industry, raw materials, packaging components, and outsourced services directly impact the safety, efficacy, and quality of the final product. A supplier audit is a...
by Dr. Yashashwini Reddy | Aug 9, 2025
Non-conformance in Pharmaceuticals Definition:Non-conformance refers to any deviation from established standards, specifications, regulatory requirements, or approved procedures in the pharmaceutical manufacturing, testing, or distribution process. Examples of...
by Dr. Yashashwini Reddy | Aug 8, 2025
What Quality Really Means for Pharmaceuticals In the pharmaceutical industry, quality means ensuring that every medicine is safe, effective, and consistent, from raw materials to the final product delivered to patients. It is not just about meeting specifications —...
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
Sampling in Cleaning Validation in Pharmaceutical Industry Cleaning Validation is a crucial part of pharmaceutical manufacturing to ensure that equipment and production areas are properly cleaned to prevent cross-contamination, ensure product quality, and comply with...
