BEGIN:VCALENDAR
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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:20260310T140000
DTEND;TZID=Africa/Johannesburg:20260310T153000
DTSTAMP:20260419T210115
CREATED:20260304T085200Z
LAST-MODIFIED:20260311T064354Z
UID:19350-1773151200-1773156600@www.sahpra.org.za
SUMMARY:Clinical Trials (Orthodox Medicines): Digital CTF1 Module & Pilot Briefing
DESCRIPTION:SAHPRA hosted a consultative meeting with industry stakeholders to share key updates on the development of the Digital CTF1 Application Module and to provide information regarding the planned pilot phase. The session included project progress updates\, a system demonstration\, and an opportunity for attendees to engage with the team. \n  \nAgenda included: \n\nProject Lifecycle Update\nDemonstration of the Digital CTF1 Application Process\nOverview of the Upcoming Pilot\n\nWatch Recording
URL:https://www.sahpra.org.za/event/clinical-trials-orthodox-medicines-digital-ctf1-module-pilot-briefing/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/03/website-mailer-banner-Clinical-Trials-Orthodox-Medicines-Digital-CTF1-Module-Pilot-Briefing.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260312T090000
DTEND;TZID=Africa/Johannesburg:20260312T120000
DTSTAMP:20260419T210115
CREATED:20260303T065554Z
LAST-MODIFIED:20260318T070727Z
UID:19347-1773306000-1773316800@www.sahpra.org.za
SUMMARY:SAHPRA’s Regulatory Technical Forum (RTF) Virtual Meeting – March 2026
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) hosted the Regulatory Technical Forum (RTF) Meeting. \nAreas of discussion on the agenda included: \n\nVeterinary Medicines\nMedical devices & IVDs\nComplementary medicines\nMedicines (Allopathic)\nInspectorate Updates\nInspectorate and Regulatory Compliance\nLegislation/Guidelines for Comment/Implementation\nIT Upgrade\n\n  \nPresentations\nVeterinary Medicines presentations \nInspectorate Updates \nNew Registrations\, Variations & Reliance \n  \nRecording
URL:https://www.sahpra.org.za/event/sahpras-regulatory-technical-forum-rtf-virtual-meeting-march-2026/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/03/mailer-website-banner-SAHPRA-Regulatory-Technical-Forum-RTF-Meeting.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260326T143000
DTEND;TZID=Africa/Johannesburg:20260326T160000
DTSTAMP:20260419T210115
CREATED:20260325T071054Z
LAST-MODIFIED:20260327T114503Z
UID:19440-1774535400-1774540800@www.sahpra.org.za
SUMMARY:Orientation Webinar on the SAHPRA Portal for New Clinical Trials Application Users
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) hosted a follow-up webinar to guide applicants through key functions on the SAHPRA Portal related to Clinical Trials applications. This practical orientation session assisted users in navigating the system effectively and completing the required actions. \n  \nTopics Covered: \n\nOrientation on registering an account on the SAHPRA Portal\nHow to create an application\nHow to create the Sales Order Form\nHow to upload proof of payment\nHow to view your Accounts Notification Centre\nHow to respond to queries from the SAHPRA unit\nHow to access your application outcome\n\n  \nRecording:
URL:https://www.sahpra.org.za/event/orientation-webinar-on-the-sahpra-portal-for-new-clinical-trials-application-users/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/03/teams-banner-Clinical-Trials-Orthodox-Medicines-Digital-CTF1-Module-Pilot-Briefing.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260413T120000
DTEND;TZID=Africa/Johannesburg:20260413T140000
DTSTAMP:20260419T210115
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:20260419T210115
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:20260419T210115
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:20260419T210115
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