Purpose: To build foundational and intermediate competence in the principles, design, and regulatory evaluation of bioavailability and bioequivalence studies for medicines registration in South Africa.
This level aims to equip learners with a sound understanding of the scientific and regulatory basis for BA–BE requirements, enabling them to support the review of dossiers and ensure that generic and reformulated medicines meet quality, safety, and efficacy standards. These materials are only accessible to those with access to the SAHPRA intranet. Please contact Learning and Development for further details.