ISO 13485 Trainingis a specialized program that provides a clear understanding of the requirements for quality management systems in the medical device industry based on ISO 13485 standards. It focuses on essential areas such as regulatory compliance, risk management, documentation control, process validation, and product traceability. The training enables participants to develop the skills needed to implement, maintain, and audit a Quality Management System (QMS) that supports the safe and consistent design, manufacturing, and distribution of medical devices. It also helps organizations meet international regulatory requirements and enhance product quality and patient safety.