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...

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

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

Hybrid

The South African Health Products Regulatory Authority (SAHPRA) recently hosted the launch webinar for our Codeine Care Initiative (CCI) series. This inaugural webinar focused on the holistic management of pain, cough, and colds. What was covered: Insightful information on pain, cold, and cough management. An...

Industry Webinar on SAHPRA’s eCTD Specification 3.0

Virtual

The South African Health Products Regulatory Authority (SAHPRA) hosted an informative workshop on the upcoming eCTD Specification 3.1 and the launch of the new Application Submission Portal. This was the first of three workshops. Presentations Download Presentation Watch Recording

CCI Webinar Series: Module 2 | Legislative Review

Hybrid

The South African Health Products Regulatory Authority (SAHPRA) hosted the 2nd webinar in our Codeine Care Initiative (CCI) series. Our first module had focused on the holistic management of pain, cough, and colds. This 2nd webinar focused on a review of legislation around codeine-containing medicines....

Industry Workshop: eCTD’s Introduction of Specification 3.1

Hybrid

The South African Health Products Regulatory Authority (SAHPRA) hosted the second industry workshop in a series of informative workshops on eCTD. This webinar introduced you to Specification 3.1. The discussion points were: Changes from Specification 3.0 Envelopes Headings Lifecycle maintenance Validations Baselines Closing sequences Presentation...

SAHPRA’s Regulatory Technical Forum (RTF) Virtual Meeting

Virtual

The South African Health Products Regulatory Authority (SAHPRA) hosted industry stakeholders at the Regulatory Technical Forum (RTF) Meeting. Areas discussed on the agenda included: Comments on the newly established SAHPRA Regulatory Technical Forum EOI on model dossiers for training BAU applications and variations Medicines (Allopathic)...

Industry Workshop: Specification 3.1 Processes

Virtual

The South African Health Products Regulatory Authority (SAHPRA) hosted the third industry workshop in a series of informative sessions around eCTD. This webinar focused on Specification 3.1 processes. The processes covered included: Baselines-Iterative TOA Splitting the eCTD Multiple applications (replicas, clones, and duplicates) Line Extensions...

SAHPRA’s Regulatory Technical Forum (RTF) Virtual Meeting

Virtual

The South African Health Products Regulatory Authority (SAHPRA) hosted industry stakeholders at the Regulatory Technical Forum (RTF) Meeting. Areas discussed on the agenda included: EOI on model dossiers for training BAU applications and variations Medicines (Allopathic) Veterinary Medicines Complementary Medicines Inspectorate and Regulatory Compliance Medical...