CIOMS and IFPMA are joining efforts to create a platform for dialog on clinical research in low- and middle-income countries. They are are convening a webinar on the importance of evolving regulatory systems and regulations to support clinical trial conduct as well as alignment to international regulatory standards.
Moderators: Zainab Aziz, Associate Director for Regulatory Affairs Policy and Strategic Operations for Sub-Saharan Africa; IFPMA Africa Regulatory Network; and Lembit Rägo, Secretary-General, Council for International Organizations of Medical Sciences
Speakers:
- Boitumelo Semete-Makokotlela, CEO, South African Health Products Regulatory Authority
- Beno Nyam Yakubu, Deputy Director, Head Clinical Trial Division, NAFDAC Nigeria. Chair of AVAREF Technical Committee
- Samvel Azatyan, Team Lead, Regulatory Convergence and Networks (RCN/REG), World Health Organization (WHO), Switzerland
- Diadié Maïga,Regional Vaccine Regulation Officer, World Health Organization Regional Office for Africa
- Imene Ben Abdallah, Country manager for Roche in Libya and Tunisia
- Fabienne Benoist, Head of Regulatory Affairs, DNDi
- Walter Jaoko, Director, KAVI Institute of Clinical Research (KAVI-ICR), University of Nairobi