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 | Apr 30, 2025
The standard color codes for gas cylinders in the pharmaceutical industry are crucial for ensuring safety, proper identification, and compliance with regulatory standards. These color codes help users quickly recognize the type of gas within a cylinder, preventing...
by Dr. Yashashwini Reddy | Apr 28, 2025
Introduction Quality is a cornerstone of the pharmaceutical industry because it directly affects patient safety, therapeutic effectiveness, and public trust. When we talk about “quality standards,” we refer to the strict guidelines, procedures, and...
by Dr. Yashashwini Reddy | Apr 23, 2025
Standard Operating Procedure (SOP) Here is a Standard Operating Procedure (SOP) for the Preservation of Control Samples of Active Ingredients. This SOP ensures that control samples of active ingredients (API) are preserved and stored in...
by Dr. Yashashwini Reddy | Apr 22, 2025
Standard Operating Procedure (SOP) Here’s a detailed Standard Operating Procedure (SOP) for Preparation of Working Standards used in analytical laboratories: 1. Purpose To describe a standardized procedure for...
