Medical Device Training Courses

Find and Register for a Medical Device Training Course to Improve Your Skills

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

Why Choose Educo Life Sciences?

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People Choose Educo Every Year

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From 180 Different Companies

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We Deliver Over 100 Courses Every Year

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We Achieve 97% Positive Feedback

Upcoming Medical Device Training Courses

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Original price was: £350.Current price is: £280.
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Team Training Solutions 

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.

 

Learn more about our team training solutions. 

Why Choose Our Medical Device Training

  • Trainer Expertise — All our instructors are industry veterans, having worked with device manufacturers, notified bodies, and regulatory agencies.
  • Practical Focus — Case studies, group workshops, and real-world examples ensure you understand how to apply theory in your projects.
  • Global Regulatory Coverage — Courses include content on UK MDR / UKCA, EU MDR / IVDR, US FDA device/IVD regulation, and harmonisation efforts.
  • Post-Learning Support — Access to reinforcement materials, learning reference guides and continuous updates helps you retain and apply your learning.
  • Flexible Delivery Formats — Choose live online, hybrid, or on-demand formats to suit your team or individual needs.

Core Medical Device and IVD Topics Covered

In our medical device & IVD training portfolio, topics include:

  • ISO 13485 & quality management systems for devices
  • Risk management & hazard analysis (ISO 14971)
  • Clinical evaluation, evidence generation, and post-market clinical follow-up (PMCF)
  • UDI, labelling, regulatory registration strategies across regions
  • Software as a Medical Device (SaMD), including AI/ML considerations
  • Biocompatibility, sterilisation, validation & verification
  • Post-market surveillance, vigilance, CAPA, complaint handling
  • Combination products (drug/device) – regulatory challenges and pathways

Who Should Attend?

Our training courses are ideal for:

  • Regulatory Affairs / QA / Compliance professionals in medical device & IVD firms
  • Design / R&D / Engineering leads working on product development
  • Clinical affairs, validation, or quality engineers seeking regulatory alignment
  • Device startups wanting to ensure compliance from the outset
  • Beginners to medical devices and/or experienced professionals
  • Commercial roles such as marketing, business development and strategy.

More Information About Our Training

Comprehensive Medical Device Training for Global Compliance

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.

Quality Systems & Risk Management as Foundation

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.

Clinical Evidence, Software & Post-Market Vigilance

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.

Device Lifecycle & Change Management

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.

Benefits & Outcomes for Your Team

Participants leave able to:

  • Prepare high-quality technical documentation and submissions
  • Understand regulatory expectations across regions
  • Align engineering, quality and RA teams on compliance strategy
  • Mitigate risk, reduce regulatory delays and audit findings
  • Maintain compliance across device lifecycles in changing regulatory environments

See What Past Attendees Think

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

Labelling and UDI for Medical Devices and IVDs

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“The course provided me with a broader idea of what is involved in the subject of labels on medical equipment & devices”

Hologic

Gathering Clinical Evidence for Medical Devices

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“I enjoyed this course so much. The trainer was vibrant, super knowledgeable and keen on help and touch all topics the attendees were interested in. Special queries were allowed. Very informative course!”

Sandoz

Medical Device Software Requirements: A Regulatory Overview

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“This course was extremely helpful! It covered lots of really detailed information in a really easy and accessible way. I have learned a lot”

University of Nottingham

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