BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//SAHPRA - ECPv6.15.20//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:SAHPRA
X-ORIGINAL-URL:https://www.sahpra.org.za
X-WR-CALDESC:Events for SAHPRA
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:Africa/Johannesburg
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0200
TZNAME:SAST
DTSTART:20250101T000000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260422T100000
DTEND;TZID=Africa/Johannesburg:20260422T120000
DTSTAMP:20260515T214229
CREATED:20260412T071948Z
LAST-MODIFIED:20260507T170753Z
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) hosted an engagement session focused on training and guidance regarding SAHPRA’s requirements for Adverse Event reporting. \n  \nThe purpose of the engagement was to enhance industry understanding and facilitate the effective implementation of Regulation 17 of the Regulations Relating to Medical Devices\, including In Vitro Diagnostic Medical Devices (IVDs). This initiative supported regulatory compliance\, strengthened post‑market surveillance activities\, and promoted the safety\, performance\, and quality of medical devices placed on the South African market. \n  \nRecording
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
END:VEVENT
END:VCALENDAR