Purpose: To introduce regulatory professionals to the fundamental principles of biostatistics and their application in the evaluation of medicines and health products.
This level aims to develop a basic understanding of statistical concepts, methods, and terminology used in regulatory science, enabling learners to interpret and apply statistical data in the assessment of preclinical, clinical, and bioequivalence studies. These materials are only accessible to those with access to the SAHPRA intranet. Please contact Learning and Development for further details.