Explore our portfolio of medical device training courses covering EU MDR, IVDR, ISO 13485, risk management, clinical evidence, and global compliance. Delivered by industry experts, our programmes help you navigate device development and regulations worldwide
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We support medical device leaders improve the technical skills and knowledge of their employees, so they are equipped to overcome challenges and meet business objectives. Working together, we design and deliver technical training courses that align with your learning requirements and business goals. For more information about how we can support your team please get in touch.
Could your medical device or IVD team benefit from any of the courses listed above? Or maybe a topic which is not highlighted? We would be happy to discuss your objectives and see how we might be able to help.
In our medical device & IVD training portfolio, topics include:
Our training courses are ideal for:
Staying ahead of evolving medical device regulations is critical. Our training programmes cover core regulations such as EU MDR 2017/745 and IVDR 2017/746, including conformity assessment, technical documentation, and post-market requirements. We also cover UK CA / UK MDR transitions, and US FDA pathways to help you navigate multi-region strategy.
A robust quality management system rooted in ISO 13485 is key to device compliance. You’ll also learn to implement effective risk management per ISO 14971, integrate design controls, and embed safety throughout device development.
Regulators expect strong clinical evaluation and evidence. You’ll dive into clinical investigations, post-market clinical follow-up, complaint handling, vigilance, and CAPA strategies. Given the rise of software-based and AI-driven devices, specific modules cover SaMD, cybersecurity, usability engineering and regulatory requirements for digital health.
Devices don’t remain static. We explore how to manage design changes, variations, upgrades, and end-of-life transitions without jeopardising compliance. You’ll also see how UDI, labelling, and traceability systems support lifecycle management.
Participants leave able to:
Understanding Biocompatibility for Medical Devices
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“For anyone in the future who needs biocompatibility training, I recommend Educo. The instructors were so informative and were able to answer all questions thrown at them”
Bedfont Scientific