Industry Webinar on Upcoming Medical Devices Voluntary Feasibility Study – Phase Two

The South African Health Products Regulatory Authority (SAHPRA) hosted a workshop on the Medical Devices Voluntary Product Registration Feasibility Study – Phase Two.

The purpose of the workshop was to engage stakeholders and discuss the Expression of Interest (EOI) process for participation in the voluntary Phase Two product registration feasibility study for medical devices.

This engagement formed part of SAHPRA’s ongoing efforts to strengthen regulatory systems, optimise registration processes, and enhance transparency in the regulation of medical devices in South Africa.