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