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....

2nd Session | Updates on Regulatory Information Management System (RIMS) Roll-Out

Virtual

The South African Health Products Regulatory Authority (SAHPRA) hosted the 2nd session of our industry webinar focused on the Regulatory Information Management System (RIMS) roll-out updates. The session was recorded and published on the SAHPRA website. A similar Update session will be held once the eSubmission specifications...

SAHPRA’s Medical Devices’ Registration Update – Upcoming Feasibility Study

Virtual

The Medical Devices Unit of the South African Health Products Regulatory Authority (SAHPRA) hosted an awareness session on this unit’s medical device registration update on the upcoming voluntary feasibility study. Date: 19 April 2024 Time: 10:00 to 13:00 Download Presentation Download Feasibility Study Watch Recording:

SAHPRA’s Regulatory Technical Forum (RTF) Inaugural Meeting

Virtual

South African Health Products Regulatory Authority (SAHPRA) hosted the Inaugural Meeting of the Regulatory Technical Forum (RTF). Areas of discussion on the agenda included: Veterinary Medicines Complementary Medicines Pharmacovigilance Medical Devices and IVDs Allopathic Medicines Radiation Control Legislation/Guidelines for Comment or Implementation Date: 16 May...

SAHPRA’s Hybrid Stakeholder Engagement Meeting

Hybrid

The South African Health Products Regulatory Authority (SAHPRA) hosted a Hybrid Stakeholder Engagement Meeting. The meeting was held in person and via our virtual platform.   Areas of discussion on the agenda included: SAHPRA’s strategy to support local manufacturing of vaccines as per African Union...

Industry Workshop on FAQs and Common Deficiencies for APIMF Submission

Hybrid

The South African Health Products Regulatory Authority (SAHPRA) hosted an industry workshop to empower and educate you on the FAQs & Common Deficiencies for APIMF Submission. The workshop provided information to the Industry Stakeholders and APIMF holders on the SAHPRA’s current APIMF submission procedure. In...

CCI Webinar Series | Module 1 | Holistic Management for pain, cough & colds

Hybrid

The South African Health Products Regulatory Authority (SAHPRA) is excited to invite you to the launch webinar for our Codeine Care Initiative (CCI) series. Our webinar series will cover various modules with our first module focused on the holistic management for pain, cough and colds....