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CALSCALE:GREGORIAN
METHOD:PUBLISH
X-ORIGINAL-URL:https://www.sahpra.org.za
X-WR-CALDESC:Events for SAHPRA
REFRESH-INTERVAL;VALUE=DURATION:PT1H
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TZID:Africa/Johannesburg
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TZOFFSETFROM:+0200
TZOFFSETTO:+0200
TZNAME:SAST
DTSTART:20250101T000000
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BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260422T100000
DTEND;TZID=Africa/Johannesburg:20260422T120000
DTSTAMP:20260419T143559
CREATED:20260412T071948Z
LAST-MODIFIED:20260412T071948Z
UID:19507-1776852000-1776859200@www.sahpra.org.za
SUMMARY:Industry Meeting on Adverse Event Reporting for Medical Devices (including IVDs)
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) invites industry stakeholders to a targeted stakeholder engagement session focused on training and guidance regarding SAHPRA’s requirements for Adverse Event reporting. \n  \nThe purpose of this engagement is to enhance industry understanding and effective implementation of Regulation 17 of the Regulations Relating to Medical Devices\, including In Vitro Diagnostic Medical Devices (IVDs). This initiative supports regulatory compliance\, strengthens post‑market surveillance activities\, and promotes the safety\, performance\, and quality of medical devices placed on the South African market. \n  \nKey areas of discussion will include: \n\nIdentification\, assessment\, and reporting of Adverse Events and near‑adverse events\nClarification of legal obligations\, reporting timelines\, submission processes\, and applicable guidelines\n\n  \nRegister here: https://bit.ly/4tcSUK6
URL:https://www.sahpra.org.za/event/industry-meeting-on-adverse-event-reporting-for-medical-devices-including-ivds/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/04/Industry-Meeting-on-Adverse-Event-Reporting-for-Medical-Devices-including-IVDs-website-email.jpg
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