REVIEW ARTICLE
31 December 2015

Medicines development and regulation in Africa

Bernd Rosenkranz1,2* Michael Reid3 Elizabeth Allen4
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1 Division of Clinical Pharmacology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, 8000, South Africa
2 Fundisa African Academy of Medicines Development, Bellville, Cape Town 7530, South Africa
3 Pfizer Laboratories (Pty) Ltd., Sandton 2196, South Africa
4 Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Rondebosch, Cape Town, 7925, South Africa
JMDS 2017 , 2(1), 33–36; https://doi.org/10.18063/jmds.v1i2.137
Submitted: 21 December 2015 | Accepted: 22 December 2015
© 2017 by the Author(s). Licensee Whioce Publishing, Singapore. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC BY-NC 4.0) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

Africa is one of the world’s fastest-growing economic regions, with a rise in its pharmaceutical industry value from $4.7 billion in 2003 to $20.8 billion in 2013. Multinational pharmaceutical companies are becoming more active in drug production and clinical trials across Africa, and there is an increase in the number of local companies engaged in medicines development and marketing. Such expansion of the local pharmaceutical industry requires trained pharmaceutical specialists to support it. The current situation and future requirements for local medicines development, regulation, education and training needs are discussed.

Keywords
medicines development
medicines regulation
Africa
training
education
PharmaTrain
IFAPP
SAHPRA
References

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Conflict of interest
No conflict of interest has been reported by the authors.
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