by Dr. Yashashwini Reddy | Apr 27, 2025
Standard Operating Procedure (SOP) 1. Purpose This SOP defines the cleaning procedure for the Automatic Distillation Apparatus to maintain its operational efficiency, avoid contamination, and ensure accurate analytical results. 2. Scope This...
by Dr. Yashashwini Reddy | Apr 27, 2025
Standard Operating Procedure (SOP) 1. Purpose This SOP describes the procedure for the proper cleaning of the dissolution tester to prevent cross-contamination, ensure equipment integrity, and maintain accuracy in dissolution testing. 2....
by Dr. Yashashwini Reddy | Oct 21, 2024
Identifying the Worst Case in Cleaning Validation In cleaning validation, determining the worst-case scenario is essential to ensure that the cleaning procedures effectively remove the most challenging residues from manufacturing equipment. This scenario represents...
by Dr. Yashashwini Reddy | Oct 3, 2024
Wash-in-Place (WIP) and Clean-in-Place (CIP) Systems in Pharmaceutical Manufacturing Introduction: In the pharmaceutical sector, maintaining cleanliness and preventing contamination is critical for product safety and regulatory compliance. Wash-in-Place (WIP) and...
by Dr. Yashashwini Reddy | Aug 28, 2024
Why Magnetic rods are used in Cleaning Verification in Pharma If you see, some regulatory agencies keep strict limits on metal contamination in pharmaceutical products. This is a very good initiative as it improves the quality of the medicines we consume. Prevention...
