Description
In this next forum, we take a look at the Medical Device and In Vitro Diagnostic Regulations in Africa and Europe and how this affects the provision of medical technologies in these areas.
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CSIR Medtech Regulatory support services and programmes with CSIR Team, led by Jeremy Wallis
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African Medical Device Regulations – an update with Lizel Dreyer-Fouche, RA Manager: Africa & Middle East, Abbott Molecular
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Overview of the European MDR and IVDR with Andre ten Napel, Regulatory Consultant, TNMC Medical Devices
Who should attend?
Regulatory personnel and those who want to gain a greater understanding of medical technology regulations
Programme
09:00 Welcome and Formalities – Madeleine Pearce, SAMED Regulatory Chair
09:05 CSIR Medtech Regulatory support services and programmes – CSIR Team, led by Jeremy Wallis
09:45 African Medical Device Regulations – an update – Lizel Dreyer-Fouche, RA Manager: Africa & Middle East, Abbott Molecular
10:20 Overview of the European MDR and IVDR – Andre ten Napel, Regulatory Consultant, TNMC Medical Devices
11:00 Close
