• Webinar on Engagement Portal – Variations and Renewal Submissions

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted a webinar to provide Industry with updates on the Engagement Portal—Variations and Renewal Submissions. Why should you attend? SAHPRA provided updates on: SAHPRA Portal roll-out Discuss the activities for variations and renewal submissions   Presentations: Engagement...

  • Webinar on Engagement Portal – General Updates for Improving User Support

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted a webinar to provide industry with updates on SAHPRA’s Engagement Portal. The session focused on various areas aimed at improving overall user support. Attendees learned about: Clarifications on industry fees Context and support volumes Visibility of...

  • SAHPRA’s Regulatory Technical Forum (RTF) Virtual Meeting – August 2025

    Virtual

    Dear Stakeholder, You are invited to the South African Health Products Regulatory Authority’s (SAHPRA’s) Regulatory Technical Forum (RTF) Meeting. Areas of discussion on the agenda include: Medicines (Allopathic) Inspectorate Updates Veterinary Medicines Complementary Medicines Inspectorate and Regulatory Compliance Medical Devices & IVDs Legislation/Guidelines for Comment/Implementation...

  • DHA Side Event | Digital Transformation of Medicines Regulation in Africa Engagement

    Hybrid [Venue: Innovation Hub]

    Inspired by the Digital Health Africa (DHA) Conference 2025, a side event on the Digital Transformation of Medicines Regulation in Africa was hosted collaboratively by the South African Health Products Regulatory Authority (SAHPRA) and Pharmacometrics Africa. The event featured insightful presentations and dynamic discussions aimed...

  • Medical Devices Webinar | Industry Meeting on Regulatory Updates and Process Improvements

    Hybrid [Venue: Innovation Hub]

    The South African Health Products Regulatory Authority (SAHPRA) hosted a consultative meeting with industry to communicate updates, compliance to legislative requirements, improve the application process, and enhance overall client service and relations. Purpose of the webinar: Update on applicable fees SAHPRA’s services and processes Annual...

  • SAHPRA’s Regulatory Technical Forum (RTF) Virtual Meeting – November 2025

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted a Regulatory Technical Forum (RTF) Meeting. Areas of discussion on the agenda included: Veterinary Medicines Medical Devices & IVDs Complementary Medicines Medicines (Allopathic) Inspectorate Updates Inspectorate and Regulatory Compliance Legislation/Guidelines for Comment/Implementation IT Upgrade   Recording

  • Clinical Trials (Orthodox Medicines): Digital CTF1 Module & Pilot Briefing

    Virtual

    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...

  • SAHPRA’s Regulatory Technical Forum (RTF) Virtual Meeting – March 2026

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted the Regulatory Technical Forum (RTF) Meeting. Areas of discussion on the agenda included: Veterinary Medicines Medical devices & IVDs Complementary medicines Medicines (Allopathic) Inspectorate Updates Inspectorate and Regulatory Compliance Legislation/Guidelines for Comment/Implementation IT Upgrade   Presentations...

  • Orientation Webinar on the SAHPRA Portal for New Clinical Trials Application Users

    Virtual

    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.   Topics...

  • Industry Meeting on Adverse Event Reporting for Medical Devices (including IVDs)

    Virtual

    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.   The purpose of the engagement was to enhance industry understanding and facilitate the effective implementation of Regulation 17 of the...