Ensure medical device quality and regulatory compliance

Learn how to implement a Medical Device Quality Management System (MDQMS).

Organizations in the medical device industry must maintain a robust and compliant quality management system to ensure product safety, meet regulatory expectations, and support global market access.

Our ISO 13485 course is designed for organizations of all types and sizes involved in the design, development, production, installation, or servicing of medical devices. It is aligned with the latest edition of the ISO 13485 standard and provides a strong foundation for preparing to implement an ISO 13485–certified Medical Device Quality Management System (MDQMS).

Our ISO 13485 course:

• Relevant for businesses establishing or improving a medical device quality management system.

• Outlines core MDQMS processes and ISO 13485 requirements.

• Provides clear guidance on the ISO 13485 certification process and audit expectations.

• Led by experienced ISO and medical device quality professionals.