The aim of this short learning programme is to introduce course participants to the theory and practice of conducting regulatory assessments of biotherapeutic and vaccine applications for registration and market access. These are complex health products and therefore SAHPRA identified the need to capacitate internal staff and external assessors in order to increase efficiency and reduce registration timelines. 

The training comprised of class room teaching by subject matter experts who also supplied training materials e.g. slides, worksheets and case studies.

These materials are only accessible to those with access to the SAHPRA intranet. Please contact your training manager for further details.