• Upcoming Workshop: QOS/QIS and Variation Validation Template

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted a workshop to share useful information on populating the QOS and QIS as a replacement for the SCoRe document, as well as information on the Variations Validation template. Date: 22 May 2023 Time: 09:00 - 11:00 Watch Recording

  • Webinar on Virtual Fee Regulation Workshop with Industry | Revised Fee Regulations

    Virtual

    South African Health Products Regulatory Authority (SAHPRA) hosted a virtual workshop in the Virtual Fee Regulation Workshop with Industry. The workshop addressed the responses to public comments and proposed changes to the Revised Fee Regulations. Thu, Feb 22, 10:00 AM - 2:00 PM (CAT)   Download...

  • Webinar on Awareness of Substandard & Falsified Medications in South Africa – Understanding Impact

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted a webinar on the Awareness of Substandard & Falsified Medications in South Africa – Understanding Impact. Key Highlights: Understanding the basics of substandard and falsified medicines Identifying the dangers of consuming untested and unauthorised medicines Importance of reporting agencies/outlets...

  • Virtual Training Session | How to use the OTC Online Medicines Directory Toolkit

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA), in conjunction with the Selfcare Association of South Africa, hosted a virtual training session on How to use the OTC Online Medicines Directory Toolkit. By registering, you have an opportunity to: grasp and understand how you can...

  • Industry Workshop | Understanding SAHPRA’s Risk Management Plan Guidelines

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted an industry workshop to empower and educate you on the Authority’s requirements when submitting Risk Management Plans (RMPs). This workshop highlighted the importance of maintaining RMPs to ensure the safety of medicines, while also sharing requirements for compliance....

  • Medical Devices Stakeholder engagement Industry Meeting

    Virtual

    A Consultative meeting with the industry to communicate updates, and improve the application process, as well as the overall services and relations. Date: 28 June 2023 Time: 9h00 to 12h30 Watch Recording

  • Complementary Medicines’ Stakeholder Engagement Hybrid Workshop

    Virtual

    The South African Health Product Regulatory Authority (SAHPRA) Complementary Medicines’ (CMs’) Hybrid Workshop successfully took place, offering attendees the option to participate either in person or via a virtual platform. Key areas discussed during the workshop included: SAHPRA responded to the 21 questions regarding Complementary...

  • Industry Stakeholder Engagement | Medical Devices Unit

    Virtual

    The Medical Devices Unit of the South African Health Products Regulatory Authority (SAHPRA) hosted a consultative meeting with Industry. The meeting aimed to communicate updates, ensure compliance with legislative requirements, discuss improvements to the application process, and enhance overall client service and relations. Areas of...

  • Radiation Control Webinar | Veterinary Licence Compliance

    Virtual

    The Radiation Control’s Licencing Unit of the South African Health Products Regulatory Authority (SAHPRA) invites you their Veterinary Licence Compliance Webinar to aid support, guidance and encourage compliance within the veterinary community. Areas of discussion include: Improve your understanding of veterinary sector compliance with the...

  • Radiation Control Webinar | Dental Licencing & Compliance

    Virtual

    The South African Health Products Regulatory Authority (SAHPRA) hosted an educational and informative webinar to provide support, guidance, and encourage compliance within the dental community throughout South Africa. Topics Covered Dental sector compliance with the Hazardous Substance act 15 of 1973 SAHPRA’s services and processes...