by Dr. Yashashwini Reddy | Jun 25, 2025
🔹 GVP Module VI – Collection, Management, and Submission of Reports of Suspected Adverse Reactions to Medicinal Products 📘 Objective: To guide Marketing Authorization Holders (MAHs), national competent authorities (NCAs), and sponsors on how to: Collect Manage...
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...
