by Dr. Yashashwini Reddy | Oct 24, 2024
Good Laboratory Practices (GLP) in the pharmaceutical industry are a set of internationally recognized standards that ensure the quality, consistency, and integrity of non-clinical studies. These practices are critical for ensuring that the data generated during drug...
by Dr. Yashashwini Reddy | Oct 18, 2024
Importance of Recalls in the Pharmaceutical Industry: Safeguarding Public Health and Compliance In the pharmaceutical industry, ensuring the safety, efficacy, and quality of drugs is of paramount importance. Despite stringent quality control measures and regulatory...
by Dr. Yashashwini Reddy | Oct 15, 2024
Standard Operating Procedure (SOP) for Cleaning of Pallets 1.0 Objective To establish the cleaning procedure for pallets used in the Manufacturing and Packing areas. 2.0 Scope This SOP applies to all pallets used in the Production department for Manufacturing and...
by Dr. Yashashwini Reddy | Oct 15, 2024
Standard Operating Procedure (SOP) for Prevention of Mix-up in the Dispensing Area 1.0 Objective This SOP outlines the steps and measures required to prevent mix-ups and ensure proper control in the dispensing area during operations. 2.0 Scope This procedure is...
by Dr. Yashashwini Reddy | Oct 10, 2024
Unveiling the Role of the Analytical Quality Assurance (AQA) Department in Pharma In the world of pharmaceuticals, quality is everything. That’s where the Analytical Quality Assurance (AQA) department steps in, ensuring that every drug produced meets strict...
