Purpose: To introduce regulatory officers, inspectors-in-training, and quality professionals to the fundamental principles and objectives of Good Manufacturing Practice (GMP) within the context of medicine regulation in South Africa.
This level focuses on developing a basic understanding of GMP concepts, terminology, and regulatory expectations, forming the foundation for future competence in inspection and compliance monitoring. These materials are only accessible to those with access to the SAHPRA intranet. Please contact Learning and Development for further details.