Best practices in the African Medicines Regulatory Harmonization initiative: Perspectives of regulators and medicines manufacturers.


Journal

PLOS global public health
ISSN: 2767-3375
Titre abrégé: PLOS Glob Public Health
Pays: United States
ID NLM: 9918283779606676

Informations de publication

Date de publication:
2023
Historique:
received: 01 04 2022
accepted: 03 04 2023
medline: 15 5 2023
pubmed: 15 5 2023
entrez: 15 5 2023
Statut: epublish

Résumé

In the African Medicines Regulatory Harmonization initiative, national regulatory authorities (NRAs) within each of Africa's regional economic communities coordinate their activities, rely on the work of one another and other trusted regulatory authorities, and apply other principles of smart regulation. The first regional medicines regulatory harmonization (MRH) initiative in Africa was launched in 2012, with the goal of accelerating access to quality, safe, effective medical products, and now five MRH initiatives are active on the continent. Thus, a wealth of knowledge regarding best practices and approaches to dealing with common challenges has accumulated. The goal of this qualitative study was to gather and share information on these best practices. To do this, we conducted interviews with key participants from four regional MRH initiatives-the East African Community (EAC), Southern African Development Community (SADC), Economic Community of West African States (ECOWAS), and Intergovernmental Authority on Development (IGAD)-as well as representatives from the pharmaceutical industry. Here we explore major themes that emerged from the interviews: 1. Transparency and reliability are critical; 2. Reliance is essential for smart regulation; 3. Multiple successful strategies for NRA capacity building have been identified; 4. Communication between heads of agencies is essential; 5. Cooperation at the regional level is not possible without leadership at the NRA level; 6. Sustainable funding remains challenging; and 7. Industry has important insights. We hope that the information on best practices shared in this article can benefit regional MRH initiatives inside and outside of Africa, ultimately helping them accelerate access to quality, safe, effective medical products.

Identifiants

pubmed: 37186241
doi: 10.1371/journal.pgph.0001651
pii: PGPH-D-22-00559
pmc: PMC10132525
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0001651

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

Copyright: © 2023 Ndomondo-Sigonda et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Margareth Ndomondo-Sigonda (M)

African Union Development Agency-New Partnership for Africa's Development, Midrand, South Africa.

Samvel Azatyan (S)

Regulatory Convergence and Networks, World Health Organization, Geneva, Switzerland.

Petra Doerr (P)

European Directorate for the Quality of Medicines & Healthcare, Strasbourg, France.

Collins Agaba (C)

CORE Consulting LTD, Mbarara, Uganda.

Kristin N Harper (KN)

Harper Health & Science Communications, LLC, Seattle, Washington, United States of America.

Classifications MeSH