Tuesday, November 11, 2025
02:00 PM - 04:00 PM
Capacity: 100 attendees
This session will explore the role of regulatory systems in strengthening clinical trial oversight and preparedness for future public health challenges. Presenters will share global experiences, best practices, and lessons learnt in ensuring ethical, efficient, and quality-assured clinical research, with a focus on building resilient and responsive regulatory frameworks across Africa.
Tendayi Arnold Kureya is a public health and research expert with over 20 years of experience in clinical trials, regula...
African Union Development Agency (AUDA-NEPAD)
Charles Sandy is a public health physician and researcher with expertise in national and regional communicable disease p...
African Centers for Diseases Control and Prevention (Africa CDC)
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CEPI
Jacqueline is a registered pharmacist in Ghana with over 17 years of healthcare experience, specializing in drug regulat...
WHO AFRO
Dr Kwasi A. Nyarko is the Coordinator of the African Vaccine Regulatory Forum (AVAREF) Secretariat, a regulatory and eth...
Dr Aboubacar Sangho is a Malian pharmacist with strong expertise in pharmaceutical regulation and ethics. He earned a Do...
Angelika Joos is a pharmacist by training. She currently is Executive Director of Science & Regulatory Policy at MSD...
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IQVIA
Kwaku Marfo is a life sciences professional with experience in clinical practice, pharmaceuticals, and global health acr...
Yodit Fitsum Ghebrezgabhier is a pharmacist and MSc Clinical Trials candidate at the University of Edinburgh, United Kin...
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AnsweredThis is going to be exciting!! Looking forward.
Designed & Implemented by
African Union Development Agency - AUDA-NEPAD
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