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The South African Health Products Regulatory Authority (SAHPRA) is a statutory body established in terms of Section 2 of the Medicines and Related Substances Act, 101 of 1965, as amended. The objects of the Authority are to provide for the monitoring, evaluation, regulation, investigation, inspection,...

As the South African Health Products Regulatory Authority (SAHPRA) embarks on the journey outlined in our Strategic Plan for 2025–2030, it is imperative to reaffirm our commitment to ensuring access to safe, effective, and high-quality health products. Guided by our reinforced vision— an agile and...

As the South African Health Products Regulatory Authority (SAHPRA) embarks on the journey outlined in our Annual Performance Plan for 2025–2026, it is imperative to reaffirm our commitment to ensuring access to safe, effective, and high-quality health products. Guided by our reinforced vision— An agile...

SAHPRA's Annual Report allows for transparency, accountability, as well as a comprehensive view of the entity’s performance and strategic direction.   View Web Version   Download PDF...

This Annual Performance Plan (APP) for the 2024/25 financial year that has been developed by SAHPRA, represents the planned actions of the Board of SAHPRA to ensure that through their considered and responsible actions, they can, together with the staff at the Authority, assure and...

AUDA-NEPAD has published its 2023 Highlights Edition on African Medicines Regulatory Harmonization (AMRH) featuring articles on: Harmony in healthcare 2023 highlights of the Good Manufacturing Practice Technical Committee Evaluation of Medicinal Products Technical Committee virtual meeting Plans for the College for African Regulatory Science Professionals ...