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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Dec 27, 2020
Australia and Oceania
The Therapeutic Goods Administration (TGA), the Australian regulating authority, has published an update regarding the ongoing process of improvement of the existing regulatory framework in the sphere of post-market monitoring and surveillance. In particular, the TGA...
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Oct 16, 2020
Asia
Taiwan Food and Drugs Administration (FDA) has published draft guidance covering the regulations related to the special measures to be taken to ensure the safety of medical devices in the context of post-market surveillance. Together with the guidance on adverse event...
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