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...
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...
The South African Health Products Regulatory Authority (SAHPRA) recently hosted its Regulatory Technical Forum (RTF) Meeting, bringing together key industry stakeholders to discuss regulatory updates. Areas of discussion on the agenda included: BAU Applications and Variations Medicines (Allopathic) Veterinary Medicines Complementary Medicines Inspectorate and Regulatory...
The South African Health Products Regulatory Authority (SAHPRA) is launching an online applications platform. This platform hosted several application processes, which are enabled across different phases in the overall implementation of their engagement platform. What was covered?: How does the portal work How to submit...
The South African Health Products Regulatory Authority (SAHPRA) hosted an educational and informative webinar to provide broader awareness of the SAHPRA Engagement Portal. This webinar session focused on the submission of Section 21 applications for Category A Medicines (also known as Orthodox or allopathic medicines)....
The South African Health Products Regulatory Authority (SAHPRA) became aware of processing issues after the launch of the SAHPRA Engagement Portal on 01 April 2025. This webinar aimed to address processing issues around system failures. Applicants are encouraged to attend to address issues regarding: Assistance...
The South African Health Products Regulatory Authority (SAHPRA) has become aware of processing issues after the launch of the SAHPRA Engagement Portal on 01 April 2025. This webinar aims to address processing issues around system failures. Applicants are encouraged to attend to address issues regarding:...
The South African Health Products Regulatory Authority (SAHPRA) has become aware of processing issues after the launch of the SAHPRA Engagement Portal on 01 April 2025. This webinar aims to address processing issues around system failures. Applicants are encouraged to attend to address issues regarding:...
The South African Health Products Regulatory Authority (SAHPRA) is hosting an Emergency Webinar to address numerous Section 21 technical queries regarding the registration of organisations/ applicants and the submission of applications. This webinar session aims to focus on the submission of Section 21 applications for...
The South African Health Products Regulatory Authority (SAHPRA) hosted a webinar to provide Industry with updates on the recently launched Engagement Portal. Why should you attend? SAHPRA will provide updates on: SAHPRA Portal roll-out Discuss the activities for the remainder of May and staggered activation...
The South African Health Products Regulatory Authority (SAHPRA) recently hosted its Regulatory Technical Forum (RTF) Meeting, which brought together key industry stakeholders to discuss regulatory updates. Areas of discussion on the agenda included: Medicines (Allopathic) Clinical Updates Veterinary Medicines Complementary Medicines Inspectorate and Regulatory Compliance...
The South African Health Products Regulatory Authority (SAHPRA) hosted a webinar to launch the NDS (National Drug Control System) Applications Portal – for import and export applications, specifically for Narcotics and Controlled Substances only. What was covered? How does the portal work How to submit...
