ISO 13485:2016 - Quality Management System for Medical Devices (QMS-MD)

This ISO 13485:2016 course provides a practical understanding of Quality Management System requirements for the medical device industry based on international standards. The course covers key concepts such as regulatory compliance, risk management, documentation, design controls, supplier management, CAPA, internal audits, and continual improvement. Designed for students, freshers, and professionals in medical devices, pharmaceuticals, healthcare, biotechnology, and related industries, this self-paced e-learning program helps learners develop skills in quality management and regulatory compliance.