Wednesday, November 12, 2025
02:00 PM - 03:30 PM
Capacity: 100 attendees
This session will explore the concept of regulatory reliance as a strategic approach to strengthen regulatory systems in Africa. Presenters will discuss how leveraging trusted assessments from other regulatory authorities can enhance efficiency, reduce duplication, and promote timely access to quality medicines across the continent.
EMA
Martin HARVEY ALLCHURCH Martin Harvey is Head of International Affairs at the European Medicines Agency since October 2...
African Union Development Agency (AUDA-NEPAD)
David Walusimbi is a pharmacist and global health professional with extensive experience in medicine regulation, academi...
Bayer
John currently serves as the Regulatory Policy and Science Lead for non-EU countries at Bayer. With a strong background ...
Union Économique et Monétaire Ouest Africaine (UEMOA)
Dr Kédji Carmelle Nadège Hounnou is a Doctor of Pharmacy with advanced expertise in pharmaceutical regulation and publ...
WHO
Mario Musonda is a pharmaceutical professional with about 15 years of experience in regulatory activities, quality manag...
FDA’s African Medicines Agency Liaison Office (AMALO)
Meisha Sampson is the first director of the FDA’s African Medicines Agency Liaison Office (AMALO), based at the U.S. E...
WHO
Nyasha Maregere is a consultant in the Special Access Programme (formerly the Facilitated Product Introduction Team) wit...
BoMRA
Dr Seima Dijeng is the Chief Executive Officer of the Botswana Medicines Regulatory Authority (BoMRA), a position he has...
Designed & Implemented by
African Union Development Agency - AUDA-NEPAD
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