Purpose : To develop advanced analytical and regulatory evaluation skills for in-depth assessment and decision-making in bioavailability and bioequivalence studies, ensuring the scientific integrity and reliability of data supporting medicine registration.
This level is designed for experienced evaluators and regulatory scientists who play a critical role in the technical review, approval, and post-market oversight of BA–BE studies submitted to SAHPRA. These materials are only accessible to those with access to the SAHPRA intranet. Please contact Learning and Development for further details.