Description
While South Africa faces its own medical device regulatory changes, we cannot lose sight of the changes happening abroad. This forum will look at the regulatory developments from across Africa as well as key considerations of the Post-Brexit medical device regulatory landscape for those trading with the UK.
- Brexit: Impact on medtech regulations and exporters to the UK – Richard Tully, Director, Compliant Medical Devices
- Africa Update: Medtech regulatory changes on the continent – Lizel Dreyer-Fouche, RA Manager: Africa & Middle East, Abbott
- SAMED draft Medical Device Regulations: progress and next steps – Madeleine Pearce, SAMED Regulatory Committee Chair
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 Committee Chair
09:05 Brexit: Impact on medtech regulations and exporters to the UK – Richard Tully, Director, Compliant Medical Devices
10:00 Africa Update: Medtech regulatory changes on the continent – Lizel Dreyer-Fouche, RA Manager: Africa & Middle East, Abbott
10:50 SAMED draft Medical Device Regulations: progress and next steps – Madeleine Pearce, SAMED Regulatory Committee Chair
11:00 Close