Pilot Project for Electronic Reporting of Serious Adverse Events (e-Reporting for Industry – VigiFlow Module)

Pilot Project for Electronic Reporting of Serious Adverse Events (e-Reporting for Industry – VigiFlow Module)

The South African Health Products Regulatory Authority (SAHPRA) invites sponsors, applicants, Clinical Research Organisations (CROs), investigators and Holders of Certificates of Registration (HCRs) conducting clinical trials to participate in a pilot project for the electronic reporting of Serious Adverse Events through the VigiFlow module (e-reporting portal).

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Document Number: CT02-2026/27
Version: 1
Date Updated: 03/08/2026
File Type: www
Category: Communication to industry
Unit: Clinical Trials