Purpose: To develop intermediate competence in the regulatory evaluation, monitoring, and management of clinical trials, focusing on practical application of Good Clinical Practice (GCP) and SAHPRA’s regulatory frameworks.
This level equips learners to critically assess trial protocols, monitor compliance, and evaluate data integrity, ensuring that clinical trials meet scientific, ethical, and regulatory standards. These materials are only accessible to those with access to the SAHPRA intranet. Please contact Learning and Development for further details.