Medtech vigilance and recall

Disclaimer: The South African Medical Technology Industry Association (SAMED) provides this content as a complimentary service. The content is not a substitute for appropriate legal advice and is not binding on SAMED. SAMED, its board members, committees, employees and members, will not be responsible for any inaccuracies or omissions, or, liable for any damages or loss of whatsoever nature suffered by any person as a result of relying on or using the content provided.

SAHPRA presentation on Vigilance and Recall
5 August 2020
The South African Health Products Regulatory Authority provided an overview of vigilance and recall of medical devices at the SAMED regulatory forum.

Adverse event practical considerations
5 August 2020
This presentation on the practical considerations for reporting on adverse events was given at the SAMED regulatory forum.

A global perspective on post-market surveillance and vigilance
5 August 2020
An overview of the global perspective on post-market surveillance and vigilance was presented at the SAMED regulatory forum.

National Vigilance Policy
18 November 2020
This presentation on the National Vigilance Policy in relation to medical technology was given at the SAMED regulatory forum.