Jun 19, 2022
Africa
The new article describes in detail certain specific aspects related to post-market surveillance – in particular, the way the authority is going to communicate important safety-related information to stakeholders. Table of...
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Jun 14, 2022
Africa
The new article describes in detail the regulatory requirements related to reporting incidents with medical devices and other healthcare products. Table of Contents The Ministry of Health of Kenya, Pharmacy and Poisons Board, has...
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May 11, 2022
Africa
The new article describes in detail the responsibilities of the parties involved in operations with medical devices in terms of post-marketing surveillance. Table of Contents The Ministry of Health of Kenya has published a guidance...
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May 1, 2022
Africa
The article provides an overview of the Kenyan regulatory requirements in the sphere of post-market surveillance for healthcare products. Table of Contents The Pharmacy and Poison Board, a division of the Kenyan Ministry of Health,...
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Mar 11, 2022
Africa
The article describes in detail the regulatory requirements related to the procedure of medical device establishment license renewal in South Africa based on the respective documents. Table of Contents The South African Health Products...
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