Call For Submission Of Qualified Person Responsible For Pharmacovigilance (QPPV) Notifications To BoMRA
Botswana Medicines Regulatory Authority (BoMRA) invites all Marketing Authorization Holders (MAHs), local technical representatives (LTRs), manufacturers and distributors of medical products to submit details of their designated Qualified Person Responsible for Pharmacovigilance (QPPV) in line with national pharmacovigilance requirements. Submission of QPPV Notifications MAHs are required to complete BoMRA QPPV Notification Form and submit the […]
Risk of Acute Pancreatitis, Including Necrotizing and Fatal Cases, Associated with GLP‑1 Receptor Agonists and Dual GLP‑1/GIP Receptor Agonists.
Botswana Medicines Regulatory Authority (BoMRA) is responsible for ensuring the safety, efficacy, and quality of medicines and related substances, including human and veterinary medicines, medical devices, and cosmetics in Botswana. In line with its ongoing surveillance of medicine safety, BoMRA wishes to draw attention to an important emerging safety concern regarding a potential risk of […]