BEGIN:VCALENDAR
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PRODID:-//SAHPRA - ECPv6.15.20//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
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
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END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260413T120000
DTEND;TZID=Africa/Johannesburg:20260413T140000
DTSTAMP:20260419T223403
CREATED:20260412T071554Z
LAST-MODIFIED:20260412T071554Z
UID:19504-1776081600-1776088800@www.sahpra.org.za
SUMMARY:Industry Meeting to receive input from applicants on the functionality of the Digital CTF1 Application Module
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) hereby invites industry stakeholders to a consultative meeting aimed at receiving updates and feedback from applicants on the functionality of the Digital CTF1 Application Module. \n  \nThe purpose of this engagement is to provide a platform for industry to share practical experiences\, challenges\, and recommendations related to the use of the SAHPRA Portal\, thereby supporting continuous system improvement and enhanced user experience. \n  \nProposed Discussion / Agenda Items: \n\nFeedback on registering an account on the SAHPRA Portal\nFeedback on how to create an application\nFeedback on how to create the Sales Order Form\nFeedback on how to upload proof of payment\nFeedback on accessing and using the Accounts Notification Centre\nFeedback on how to respond to queries from the relevant SAHPRA unit\nFeedback on how to access application outcomes\n\nRegister here: https://bit.ly/4ceXW1i
URL:https://www.sahpra.org.za/event/industry-meeting-to-receive-input-from-applicants-on-the-functionality-of-the-digital-ctf1-application-module/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/04/Industry-Meeting-to-receive-input-from-applicants-on-the-functionality-of-the-Digital-CTF1-Application-Module-website-mailer.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260416T140000
DTEND;TZID=Africa/Johannesburg:20260416T150000
DTSTAMP:20260419T223403
CREATED:20260415T054921Z
LAST-MODIFIED:20260416T164838Z
UID:19525-1776348000-1776351600@www.sahpra.org.za
SUMMARY:Webinar on AEFI Reporting & Launch of VigiMobile App for HCPs
DESCRIPTION:The South African Health Products Authority (SAHPRA) hosted a Webinar on reporting of Adverse Effects Following Immunisation (AEFI) and Launch of the VigiMobile App for Healthcare Professionals (HCPs). \nAEFI surveillance is a key component of the National Expanded Programme on Immunisation (EPI) and depends on timely and accurate reporting by healthcare professionals. \nTo strengthen AEFI reporting\, SAHPRA\, in collaboration with the National Department of Health\, has introduced electronic submission of AEFI reports. This Webinar will assist healthcare professionals to understand basic concepts of AEFI and reinforce the importance of reporting both non-serious and serious AEFIs. \nThe Webinar addressed the following topics: \n\nUnderstanding Basic Concepts and Reporting of Adverse Events Following Immunisation\nDemonstration of AEFI reporting using the VigiMobile App\n\n  \nRecording:
URL:https://www.sahpra.org.za/event/webinar-on-aefi-reporting-launch-of-vigimobile-app-for-hcps/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/04/Pharmacovigilance-Unit-_-Understanding-Basic-Concepts-and-Reporting-of-Adverse-Events-Following-Immunisation-mailer-16-April.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260420T140000
DTEND;TZID=Africa/Johannesburg:20260420T150000
DTSTAMP:20260419T223403
CREATED:20260415T055241Z
LAST-MODIFIED:20260415T055241Z
UID:19528-1776693600-1776697200@www.sahpra.org.za
SUMMARY:Webinar on AEFI Reporting & Launch of VigiMobile App for HCPs
DESCRIPTION:The South African Health Products Authority (SAHPRA) will host a Webinar on reporting of Adverse Effects Following Immunisation (AEFI) and Launch of VigiMobile App for Healthcare Professionals (HCPs). \nAEFI surveillance is a key component of the National Expanded Programme on Immunisation (EPI) and depends on timely and accurate reporting by healthcare professionals. \nTo strengthen AEFI reporting\, SAHPRA\, in collaboration with the National Department of Health\, has introduced electronic submission of AEFI reports. This Webinar will assist healthcare professionals to understand basic concepts of AEFI and reinforce the importance of reporting both non-serious and serious AEFIs. \nThe Webinar will address the following topics: \n\nUnderstanding Basic Concepts and Reporting of Adverse Events Following Immunisation\nDemonstration of AEFI reporting using the VigiMobile App\n\nWe look forward to having you attend this event! \n  \nRegister here: https://bit.ly/47V7RYD
URL:https://www.sahpra.org.za/event/webinar-on-aefi-reporting-launch-of-vigimobile-app-for-hcps-2/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/04/Pharmacovigilance-Unit-_-Understanding-Basic-Concepts-and-Reporting-of-Adverse-Events-Following-Immunisation-teams-20-april.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260422T100000
DTEND;TZID=Africa/Johannesburg:20260422T120000
DTSTAMP:20260419T223403
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
END:VEVENT
END:VCALENDAR