![TMDA Guidance on Changes to Medical Devices: Overview](https://www.regdesk.co/wp-content/uploads/2022/08/medical-workers-hand-wearing-surgical-glove-holding-tanzania-flag-heart-236683017.jpeg)
Aug 7, 2022
Africa
The article provides an overview of the regulatory requirements related to changes to medical devices already placed on the market. Table of Contents The Tanzania Medicines and Medical Devices Authority (TMDA), a country’s regulatory agency in the sphere of...
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![Tanzanian Draft Regulation on Laboratory Analysis](https://www.regdesk.co/wp-content/uploads/2021/05/TMDA-Tanzania.jpg)
May 12, 2021
Africa
Tanzania Medicines and Medical Devices Authority (TMDA), the country’s agency responsible for healthcare products, has published a draft regulation prescribing the rules and procedures for laboratory analysis of medical and non-medical products. The new draft...
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![NDDA Notice on Sample Collection Rules for Medical Devices](https://www.regdesk.co/wp-content/uploads/2020/12/kazakistan-1080x675.jpg)
Feb 8, 2021
Africa
The National Center for Expertise of Medicines and Medical Devices (NDDA), Kazakhstan’s body responsible for the assessment of quality and safety of medical devices, has published an official notice on the rules prescribing the collection of samples to be...
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![Tanzania on Storage and Distribution of Medical Devices](https://www.regdesk.co/wp-content/uploads/2021/02/tanzania-flag-std_1-800x675.jpg)
Feb 8, 2021
Africa
The Tanzania Medicines & Medical Devices Authority (TMDA), the country’s regulating authority responsible for healthcare products, has published a draft regulation on good storage and distribution practices with regard to medicines and medical devices. Regulatory...
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