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

    Virtual

    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.   The purpose of this engagement is to enhance industry understanding and effective implementation of Regulation 17...

  • Industry Webinar on Upcoming Medical Devices Voluntary Feasibility Study – Phase Two

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) invites industry stakeholders to attend a workshop on the upcoming Medical Devices Voluntary Product Registration Feasibility Study – Phase Two.   The purpose of this workshop is to engage stakeholders and discuss the Expression of Interest (EOI) process for participation in the voluntary...