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

The South African Health Products Regulatory Authority (SAHPRA) invites industry stakeholders to attend a workshop on the upcoming Medical Devices Voluntary Product Registration Feasibility Study – Phase Two.

The purpose of this workshop is 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 forms 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.

Discussion topics will include:

• Overview of the Phase Two Product Registration Feasibility Study
• Vector submission process and portal for applications

Register here: https://bit.ly/4tw7MTQ