Optimizing the East African Community’s Medicines Regulatory Harmonization initiative in 2020–2022: A Roadmap for the Future


Autoři: Mawien Arik aff001;  Emmanuel Bamenyekanye aff002;  Adam Fimbo aff003;  Joseph Kabatende aff004;  Agnes Sitta Kijo aff003;  Burhani Simai aff005;  Fred Siyoi aff006;  Samvel Azatyan aff007;  Aggrey Ambali aff008;  Emer Cooke aff007;  Jane H. Mashingia aff009;  John Patrick Mwesigye aff009;  Margareth Ndomondo-Sigonda aff008;  Hiiti Sillo aff007;  Stanley Sonoiya aff009;  Paul Tanui aff008;  Mike Ward aff007;  Thomas Delano aff010
Působiště autorů: Drug and Food Control Authority, Juba, South Sudan aff001;  Directorate of Pharmacy, Medicines, and Laboratories, Bujumbura, Burundi aff002;  Tanzania Medicines and Medical Devices Authority, Dar Es Salaam, Tanzania aff003;  Rwanda Food and Drugs Authority, Kigali, Rwanda aff004;  Zanzibar Food and Drug Agency, Zanzibar City, Zanzibar aff005;  Pharmacy and Poisons Board, Nairobi, Kenya aff006;  World Health Organization, Geneva, Switzerland aff007;  African Union Development Agency–New Partnership for Africa’s Development, Midrand, South Africa aff008;  East African Community Secretariat, Arusha, Tanzania aff009;  Boston Consulting Group, Paris, France aff010
Vyšlo v časopise: Optimizing the East African Community’s Medicines Regulatory Harmonization initiative in 2020–2022: A Roadmap for the Future. PLoS Med 17(8): e32767. doi:10.1371/journal.pmed.1003129
Kategorie: Collection Review
doi: 10.1371/journal.pmed.1003129

Souhrn

Margareth Ndomondo-Sigonda outlines future challenges for the East African Medicines Regulatory Harmonization initiative.

Klíčová slova:

Africa – Drug regulation – Drug safety – HIV vaccines – Marketing – Medical devices and equipment – Rheumatology – Tanzania


Zdroje

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PLOS Medicine


2020 Číslo 8

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