by Dr. Yashashwini Reddy | May 7, 2025
Standard Operating Procedure (SOP) 1. Objective To establish a standardized method for the safe and efficient operation of the 20-station single rotary tablet compression machine, ensuring consistent tablet quality and compliance with Good...
by Dr. Yashashwini Reddy | May 7, 2025
Standard Operating Procedure (SOP) 1. Objective To establish a standardized method for the safe and efficient operation of the 27-station double rotary tablet compression machine, ensuring consistent tablet quality and compliance with Good...
by Dr. Yashashwini Reddy | May 7, 2025
Here’s a comprehensive Standard Operating Procedure (SOP) for the operation of a Rapid Mixer Granulator (RMG), tailored for pharmaceutical manufacturing environments: Standard Operating Procedure (SOP) 1.0 Objective To establish a...
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
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 /...
