This introductory course to Medical Devices will walk you through the main aspects of medical device development and the regulatory requirements for Medical Devices around the world.

In this training course you will be presented with an overview of the ISO 13485 standard and the main requirements of a Quality System for Medical Device companies.

In this comprehensive risk management course you will acquire all necessary skills to create, develop and maintain a Risk Management File for medical devices based on the requirements of ISO 14971.

In this base course of IEC 62304 you will acquire knowledge on the different aspects of the medical device software lifecycle processes.

In this introductory course on the cybersecurity requirements for Medical Devices you will receive a detailed overview of the different regulations, standards, guidance documents and requirements.