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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: $479.Current price is: $383.
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$383 $479Price range: $383 through $479
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Original price was: $479.Current price is: $383.
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Original price was: $814.Current price is: $651.
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Original price was: $1,909.Current price is: $1,361.
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Bespoke Medical Device Training Covering MDR, ISO 13485, and Global Compliance

Need to build medical device expertise across your organisation? We deliver tailored training programmes covering EU MDR, IVDR, ISO 13485, risk management, clinical evidence, regulatory submissions, and global market access for devices and IVDs. Our team training is designed around your product portfolio and your team’s specific development needs.

What Does Our Medical Device Team Training Cover?

Our medical device team training programmes cover the full breadth of device development and compliance — from regulatory affairs and quality management through to clinical evaluation, post-market surveillance, and technical documentation. We can deliver focused workshops on specific standards (ISO 13485, ISO 14971, IEC 62304) or broader programmes that take your team through the entire device lifecycle from concept to market. For more specialist requirements, we also offer dedicated training in medical device regulatory affairs, clinical evaluation and CER writing, IVD and IVDR compliance, and PRRC training.

Medical Device Training for MDR Transition and Beyond

Whether you’re navigating the MDR transition, preparing for FDA submissions, building an internal training academy, or upskilling a newly formed regulatory team, we’ll design a programme that fits your organisation’s size, product portfolio, and experience level. Training can be delivered live online, in-person, or as a hybrid programme across multiple sessions. Learn more about our team training approach or get in touch to discuss your requirements.

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

Free Medical Device Resources

We provide a wealth of free resources designed to elevate your career in medical devices. Delve into our exclusive free trainer interviews, thought-provoking articles, career advice and much more below.

Medical Devices & IVDs Free Module 1 Training Sessions

Medical Devices & IVDs Free Module 1 Training Sessions

Free Module 1 Training for Medical Device & IVD Professionals

Many of our medical device and IVD training courses offer a free-to-attend Module 1, giving you valuable insights and a preview of the full course experience. Browse the available courses below and register using the form provided. Once registered, you'll receive joining instructions for the...

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Essential Guide to Clinical Evidence for Medical Devices in the EU

Essential Guide to Clinical Evidence for Medical Devices in the EU

Explore Key Standards and Guidance Documents

Introduction: The Role of Clinical Evidence in Medical Device Compliance In the European Union, gathering clinical evidence for medical devices is essential to regulatory compliance, particularly under the Medical Device Regulation (MDR). Clinical evidence helps demonstrate that a device is safe, performs as intended, and…

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From 510(k) to PMA: Choosing the Right FDA Submission Pathway for Your Medical Device

From 510(k) to PMA: Choosing the Right FDA Submission Pathway for Your Medical Device

Your step-by-step guide to the FDA’s 510(k), De Novo, and PMA submission routes.

Navigating the U.S. Food and Drug Administration (FDA) regulatory process can be one of the most challenging steps for medical device manufacturers aiming to enter the American market. Unlike the European system, where the CE marking process is guided by Notified Bodies under the Medical...

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The EU AI Act and Medical Devices: What MedTech Companies Must Do Before August 2026

Understanding high-risk AI classification, data governance requirements and lifecycle compliance for AI-enabled medical devices in Europe.

Artificial intelligence is no longer a future-facing concept in medical technology — it is already embedded in diagnostic imaging, clinical decision support, digital pathology, wearable monitoring systems and predictive modelling tools. However, as AI capability has accelerated, so too has regulatory scrutiny. The introduction of...

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What is UDI (Unique Device Identification)?

What is UDI (Unique Device Identification)?

Learn More About UDI Labelling for Medical Devices

The Unique Device Identification (UDI) system is a globally recognised framework designed to provide a unique identifier for medical devices, enhancing traceability and safety within healthcare. It has become a cornerstone of regulatory efforts in both the United States and Europe, ensuring that medical devices,…

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Comprehensive Guide to Chemical Characterisation and Biocompatibility in Medical Devices

Comprehensive Guide to Chemical Characterisation and Biocompatibility in Medical Devices

Understand Chemical Characterisation to Ensure a Safe and Compliant Medical Device

In the medical device industry, ensuring safety and compliance with regulatory standards is paramount. Chemical characterisation and biocompatibility testing are essential steps in this process, guided by frameworks such as ISO 10993. These evaluations help manufacturers understand the materials in their devices and assess potential…

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