BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//SAHPRA - ECPv6.17.0//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
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260522T100000
DTEND;TZID=Africa/Johannesburg:20260522T120000
DTSTAMP:20260522T110157Z
CREATED:20260512T082546Z
LAST-MODIFIED:20260522T110157Z
UID:19693-1779444000-1779451200@www.sahpra.org.za
SUMMARY:Webinar on Medical Device Licencing & Compliance
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) hosted a stakeholder engagement webinar focused on medical device licensing and compliance requirements. \nThe purpose of the engagement was to provide targeted training to industry stakeholders on SAHPRA’s regulatory requirements\, supporting improved compliance and effective implementation across the sector. \n  \nRecording
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
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260622T090000
DTEND;TZID=Africa/Johannesburg:20260622T120000
DTSTAMP:20260715T063852Z
CREATED:20260619T104332Z
LAST-MODIFIED:20260715T063852Z
UID:19938-1782118800-1782129600@www.sahpra.org.za
SUMMARY:SAHPRA’s Regulatory Technical Forum (RTF) Virtual Meeting – June 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  \nDownload Presenatations \n  \nRecording
URL:https://www.sahpra.org.za/event/sahpras-regulatory-technical-forum-rtf-virtual-meeting-june-2026/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/06/mailer-banner-SAHPRA-Regulatory-Technical-Forum-RTF-Meeting.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260629T130000
DTEND;TZID=Africa/Johannesburg:20260629T150000
DTSTAMP:20260630T104625Z
CREATED:20260624T082045Z
LAST-MODIFIED:20260630T104625Z
UID:19949-1782738000-1782745200@www.sahpra.org.za
SUMMARY:Webinar on Import Authorisation Requirements for Health Products Importers
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) hosted a webinar on the Introduction of Import Authorisation Requirements for Health Products Importers. \n  \nAs part of aligning with WHO Global Benchmarking Tool (GBT) Maturity Level 3 (ML3)\, the SAHPRA is introducing a mandatory Import Authorisation System for all health product importers\, with a pilot phase commencing 1 September 2026. This system aims to strengthen regulatory oversight\, improve product traceability\, and safeguard public health. \n\n\n\n\n\nKey Discussion Areas\n\nWHO GBT ML3 overview\nScope of affected products and importers\nApplication and approval process\nFees and payment modalities\nImplementation timeline and FAQs\n\n\n\n  \nPre-Import Authorisation presentation \n\n  \nRecording
URL:https://www.sahpra.org.za/event/webinar-on-import-authorisation-requirements-for-health-products-importers/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/06/mailer-website-banner-Webinar-on-the-Introduction-of-Import-Authorisation-Requirements-for-Health-Products-Importers.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Africa/Johannesburg:20260629T130000
DTEND;TZID=Africa/Johannesburg:20260629T150000
DTSTAMP:20260716T094620Z
CREATED:20260716T094515Z
LAST-MODIFIED:20260716T094620Z
UID:20038-1782738000-1782745200@www.sahpra.org.za
SUMMARY:Industry Webinar on Updates to the Variations Guideline and Codes
DESCRIPTION:The South African Health Products Regulatory Authority (SAHPRA) invites industry stakeholders to attend a Webinar on the Updates to the Variations Guideline and Codes. \n  \nThe webinar aims to inform stakeholders of the updates to the Variations Guideline and associated codes\, and to provide guidance on the technical changes contained within the revised guideline. \n  \nWhat to expect: \n\nBrief introduction to the updated Variations Guideline.\nHand over to each unit to guide industry stakeholders through the technical changes in their respective sections of the guideline.\n\n  \nWe encourage all relevant industry stakeholders to participate in this important session. \n  \n\nRegister here
URL:https://www.sahpra.org.za/event/industry-webinar-on-updates-to-the-variations-guideline-and-codes/
LOCATION:Virtual
CATEGORIES:Meeting,Webinar
ATTACH;FMTTYPE=image/jpeg:https://www.sahpra.org.za/wp-content/uploads/2026/07/mailer-baner-Industry-Meeting-on-Updates-to-the-Variations-Guideline-and-Codes-.jpg
END:VEVENT
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