by Dr. Yashashwini Reddy | Apr 26, 2025
Standard Operating Procedure (SOP) 1. Purpose To outline the procedure for investigating failures in processes, systems, products, or equipment to determine root causes, implement corrective actions, and prevent recurrence. 2. Scope This SOP...
by Dr. Yashashwini Reddy | Nov 28, 2024
Basic Guidelines for Process Validation in Tablet Manufacturing Process validation is a critical component of pharmaceutical manufacturing that ensures each batch of tablets meets quality, safety, and efficacy standards. The following guidelines outline the...
by Dr. Yashashwini Reddy | Oct 18, 2024
Developmental Quality Assurance (DQA) in Pharmaceuticals The Developmental Quality Assurance (DQA) department plays a crucial role in ensuring the quality and compliance of pharmaceutical products during their development phase. This department works alongside...
by Dr. Yashashwini Reddy | Oct 18, 2024
Role of the Technology Transfer Department in the Pharmaceutical Industry The Technology Transfer (TT) department is essential in moving pharmaceutical products from development to full-scale manufacturing. Their primary role is to ensure a seamless transfer of...
by Srikanth | Aug 31, 2024
What is Pharmacovigilance? Pharmacovigilance, as defined by the World Health Organization (WHO), refers to the science and activities related to identifying, assessing, comprehending, and preventing adverse reactions or other drug-related problems. Aims of...
