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Sahpras Industry Consultation On E Reporting Vigiflow Platform
South African Health Products Regulatory AuthorityRef: https://www.sahpra.org.za/event/sahpras-industry-consultation-on-e-reporting-vigiflow-platform/
Official source
Source domain: sahpra.org.za
Collected on 3 August 2026
Always confirm details on the official source before acting.
What this means
This document is an SAHPRA event listing/invitation for an industry consultation webinar on the implementation of the Vigiflow industry e-reporting platform. SAHPRA invites holders of certificates of registration (HCRs) and clinical research organisations (CROs) that submit adverse events (AEs) and/or serious adverse events (SAEs) to a virtual meeting to clarify postmarketing AE submissions and to introduce a similar Vigiflow tool for submitting SAEs during clinical trials. The webinar is scheduled for 4 August from 2:00 pm to 4:00 pm, and SAHPRA provides links to register and download an agenda.
Facts
Reference
https://www.sahpra.org.za/event/sahpras-industry-consultation-on-e-reporting-vigiflow-platform/
Key Takeaways
- Organisation: South African Health Products Regulatory Authority (SAHPRA)
- Event: Industry Consultation on e-Reporting Vigiflow Platform
- Audience: Holders of certificates of registration (HCRs) and clinical research organisations (CROs) submitting AEs/SAEs
- Purpose: Clarify postmarketing AE submissions via Vigiflow and introduce Vigiflow tool for SAEs during clinical trials
- Platform description: Web-based tool for submitting ICSR, AEFI, and SAEs to SAHPRA’s national database using an international standardised format
- Date: August 4
- Time: 2:00 pm - 4:00 pm
- Venue: Virtual
- Agenda: Available to download (link provided)
- Registration: Register link provided
- South African Health Products Regulatory Authority (SAHPRA)
- Holders of certificates of registration (HCRs)
- Clinical research organisations (CROs)