SAHPRA invited stakeholders to participate in the Medical Devices Product Registration Feasibility Study and related activities. The engagement focused on collaborating with industry stakeholders on regulatory matters concerning the preliminary report on product registration feasibility, as well as other communication and position documents published by...
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
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...
