by Dr. Yashashwini Reddy | May 6, 2025
Here’s a detailed checklist for auditing an ointment manufacturing facility, aligned with Good Manufacturing Practices (GMP), regulatory expectations (such as USFDA, WHO, EU-GMP), and quality standards. The checklist is categorized for clarity: 1. General...
by Dr. Yashashwini Reddy | May 5, 2025
Working and Principle of Rapid Mixer Granulator (RMG) – Detailed Explanation A Rapid Mixer Granulator (RMG) is a high-performance industrial equipment widely used in the pharmaceutical industry for mixing and granulation of powders to form granules. This process is...
by Dr. Yashashwini Reddy | May 3, 2025
Lubricants in Pharmaceutical Tablets: Their Role in Ensuring Efficiency and Quality Lubricants play a critical role in the formulation and manufacturing of pharmaceutical tablets. They are essential additives that significantly enhance the efficiency of the tablet...
by Dr. Yashashwini Reddy | May 2, 2025
Structure of a URS Document for Pharmaceutical Equipment A well-structured URS should include the following key sections: 1. Title Page Document title (e.g., “User Requirement Specification for [Equipment Name]”) Document number and version Prepared by /...
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...
