16 Jul Contact Details for Guideline SAHPGL-MD-03 Medical Device Vigilance: Adverse Events Reporting for License Holders
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This document is intended to provide contact details for communicating reportable adverse events, as per Guideline SAHPGL-MD-03, as well as contact details for any Recalls and Market actions for medical devices (including IVDs).
Reportable adverse event reports must be emailed to: mdvigilance@sahpra.org.za.
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Document Number:
MD01-2024/2025
Version:
1
Date Updated:
16/07/2025
File Type:
pdf
Category:
Communication to industry