Medical device regulations/ guidelines for West Africa

Regional Regulatory Affairs & Scientific Office Manager at Mundipharma International Limited

January 2016

< 1 min reading time

Hi Colleagues!
Does anyone have the medical device regulations/ guidelines for West Africa (Ivory Coast, Senegal, Mali, Cameroon, and Gabon)?
How long does it approximately take to complete the registration process especially for Class IIb and III medical devices?
Thanks!

source: https://www.linkedin.com/groups/78665/78665-6097822895587815428

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Posted by Dr Fatima Zaid Abu Zanat

Asked on January 26, 2016 12:00 am

1594 views

like 4 comments

	Private answer Have you considered contacting NAMSA for guidance? They offer regulatory services: http://www.namsa.com/Services/Core-Services/Regulatory-Consulting Marked as spam like Report spam
	Private answer Most french speaking african countries should accept the CE mark if you have it already. Contact the Ministry of Health for more of respective countries for more info Marked as spam like Report spam
	Private answer Ikbal Errih, M.D Machlab Ali Marked as spam like Report spam
	Private answer Ikbal Errih, M.D CE mark is enough to start your process Marked as spam 1 like Report spam

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