African Medicines Agency calls for stronger regulatory cooperation to improve access to safe medicines

Date: 2026-10-29
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By:   Nana Appiah Acquaye

The African Medicines Agency (AMA) has called for stronger cooperation among national regulatory authorities across Africa to improve access to safe, effective and quality-assured medical products, while reducing duplication in regulatory processes.

AMA Director General Dr. Delese Mimi Darko made the call during the inaugural AMA Week in Kigali, Rwanda, where she met with heads of African National Regulatory Authorities (NRAs) to discuss strengthening cooperation and advancing shared regulatory priorities.

Darko said national regulatory authorities were the foundation of a strong African Medicines Agency, which was established to build on their strengths and bring them together.

She said she was encouraged by the commitment of members of the Network of Heads of African NRAs to shaping the future of AMA, including discussions on how the Network should function, continued support for the ratification of the AMA Treaty and efforts to strengthen cooperation among members.

“We must continue building trust and greater reliance among our national regulatory authorities,” Darko said.

She noted that Africa had considerable regulatory expertise across its Member States and that sharing this expertise, relying on one another’s scientific work and reducing unnecessary duplication could help establish a more efficient and harmonised regulatory system.

Darko emphasised that AMA was established to strengthen and complement national regulatory authorities, not replace them, adding that national authorities remained central to regulatory decision-making.

She said AMA’s role was to support their capacities, facilitate cooperation and build on the work they were already doing.

The meeting marked the second gathering of the Network of Heads of African NRAs, following its first meeting in January this year. Since then, AMA has launched the AfriVigilance platform and developed the Regulatory Rapid Alert and Information Network to facilitate the exchange of safety information and strengthen collective responses to substandard and falsified medical products.

“These are practical examples of what we can achieve when we connect our national regulatory systems and work together,” Darko said.

During the meeting, Darko congratulated Professor Mojisola Christianah Adeyeye, Director General of Nigeria’s National Agency for Food and Drug Administration and Control (NAFDAC), on her election as Chair of the Network.

She also congratulated Dr. Ange Mibindzou Mouelet, Director General of Gabon’s Agence Nationale du Médicament et des Autres Produits de Santé, on his election as Co-Chair.

Darko expressed her appreciation to the heads of national regulatory authorities for their leadership, commitment and continued confidence in AMA, and said she looked forward to working closely with the Network’s members to advance their shared priorities.

 

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