The Ministry of Health approved a new regulation that will facilitate the sale of medical cannabis products to help patients who urgently need them to...
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A collection of guidance has been published by the Medicines and Healthcare products Regulatory Agency (MHRA) to update manufacturers of medical devices on new regulations. The Post-market surveillance (PMS) regulation for medical devices in Great Britain which will come into force on 16 June 2025. Its key new requirements are enhanced data collection, shorter timelines […]
The Ministry of Health approved a new regulation that will facilitate the sale of medical cannabis products to help patients who urgently need them to...
The Ghana Food and Drugs Authority (FDA) has spearheaded a joint initiative with National Regulatory Authorities (NRAs) in seven African countries to...
This update aims to ensure the quality of fertilizers, streamline regulatory processes, and facilitate the import of certified products from...
The African Union Development Agency – New Partnership for Africa’s Development (AUDA-NEPAD) and Africa Centres for Disease Control and...
WASHINGTON — February 21, 2025 — The American Medical Manufacturers Association (AMMA) is committed to ensuring the resilience of America’s...
DEADLINE: 27TH FEBRUARY, 2025EDO STATE HOSPITALS MANAGEMENT AGENCY ESSENTIAL DRUGS PROGRAMMEINVITATION FOR PRE-QUALIFICATION FOR THE PROCUREMENT OF...
By Kolja Brockmann and Lauriane Héau For all their legitimate law-enforcement and intelligence-gathering uses, cyber-surveillance tools are...