BEGIN:VCALENDAR
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METHOD:PUBLISH
X-WR-CALNAME:SAHPRA
X-ORIGINAL-URL:https://www.sahpra.org.za
X-WR-CALDESC:Events for SAHPRA
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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:20260513T201352
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:20260513T201352
CREATED:20260415T054921Z
LAST-MODIFIED:20260423T050645Z
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:20260513T201352
CREATED:20260415T055241Z
LAST-MODIFIED:20260423T050707Z
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) 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-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:20260513T201352
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
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260508T110000
DTEND;TZID=Africa/Johannesburg:20260508T130000
DTSTAMP:20260513T201352
CREATED:20260428T112633Z
LAST-MODIFIED:20260511T070434Z
UID:19653-1778238000-1778245200@www.sahpra.org.za
SUMMARY:Industry Webinar on Upcoming Medical Devices Voluntary Feasibility Study - Phase Two
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) hosted a workshop on the Medical Devices Voluntary Product Registration Feasibility Study – Phase Two. \n  \nThe purpose of the workshop was to engage stakeholders and discuss the Expression of Interest (EOI) process for participation in the voluntary Phase Two product registration feasibility study for medical devices. \n  \nThis engagement formed part of SAHPRA’s ongoing efforts to strengthen regulatory systems\, optimise registration processes\, and enhance transparency in the regulation of medical devices in South Africa. \n\n  \nRecording\n \n  \nPresentations \nMD Registration Feasibility Study Phase 2
URL:https://www.sahpra.org.za/event/industry-webinar-on-upcoming-medical-devices-voluntary-feasibility-study-phase-two/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/04/mailer-website-Medical-Devices-Unit-Industry-Webinar-on-Product-Registration-Feasibility-and-Related-Activities-v2.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260520T100000
DTEND;TZID=Africa/Johannesburg:20260520T110000
DTSTAMP:20260513T201352
CREATED:20260508T181647Z
LAST-MODIFIED:20260508T181647Z
UID:19684-1779271200-1779274800@www.sahpra.org.za
SUMMARY:Launch of the Prescription-Only Medicines Section – SAHPRA Online Medicines Directory
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) cordially invites you to attend the official online launch of the Prescription-Only Medicines (Rx) Section of the SAHPRA Online Medicines Directory. \n  \nSAHPRA successfully launched the Over-the-Counter (OTC) Online Medicines Directory in June 2022 as the first phase of this initiative. \n  \nThe Online Medicines Directory is designed to provide patients\, consumers\, and healthcare providers with a single\, trusted and authoritative source of information on all medicines approved by SAHPRA. \n  \nThe launch of the Rx section marks a significant milestone in expanding access to comprehensive\, reliable medicine information in South Africa. \nRegister here: https://bit.ly/4fgcyAq
URL:https://www.sahpra.org.za/event/launch-of-the-prescription-only-medicines-section-sahpra-online-medicines-directory/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/05/MAILER-Launch-of-the-Prescription-Only-Medicines-Section-–-SAHPRA-Online-Medicines-Directory.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260522T100000
DTEND;TZID=Africa/Johannesburg:20260522T120000
DTSTAMP:20260513T201352
CREATED:20260512T082546Z
LAST-MODIFIED:20260512T082839Z
UID:19693-1779444000-1779451200@www.sahpra.org.za
SUMMARY:Webinar on Medical Device Licencing & Compliance
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) cordially invites you to attend a stakeholder engagement webinar focused on medical device licensing and compliance requirements. \n  \nThe purpose of this engagement is to provide targeted training to industry stakeholders on SAHPRA’s regulatory requirements\, supporting improved compliance and effective implementation across the sector. \n  \nDiscussion topics will include: \n\nApplication processes\, including updates to relevant forms\nProgress on ISO 13485 certification post-implementation\nAnnual retention fees\nPort of entry requirements\n\n\n  \nStakeholders are encouraged to attend and actively participate in this important session. \n  \nShould you require further information\, please do not hesitate to contact us. \n  \nWe look forward to your participation. \n\n  \nRegister here
URL:https://www.sahpra.org.za/event/webinar-on-medical-device-licencing-compliance/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/05/mailer-Medical-Devices-Unit-Industry-Webinar-on-Product-Registration-Feasibility-and-Related-Activities.jpg
END:VEVENT
END:VCALENDAR