MDTI is part of the Knowledge & Networking Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.


Free-to-access Webinars

Live & recorded webinars by leading medical device experts


MDTI has joined with leading experts in the medical devices industry to bring you a variety of free-to-access webinars to provide you with a taster of what our training courses can offer. Our webinars range from 5 – 30 minutes and cover a wide range of topics including Clinical Evaluations and European Regulation of In Vitro Classification. We run these interactive live webinars every month which we then upload to our YouTube Channel and website.

Benefits of MDTI webinars:

  • Free registration
  • Q&A session with webinar trainer
  • Exclusive insight into topical content

If you would like to recommend a topic for a webinar, please email and we will try and accommodate your preferences.

For sponsorship enquiries regarding our webinars, please contact Michael Hanton via or +44 20 701 76406.

For suggestions on topics you would like to see on our platform please contact our producer.

Free-to-access Webinars

Navigating Pricing and The Reimbursement Landscape in Europe

Over c 30 minutes, Emmanuel Garnier (Lawyer at Simmons & Simmons), a specialist in advising clients on pricing and reimbursement strategies, talks through pathways in France, Germany and the UK.

Medical devices software development and applications

Over c.30 minutes, this webinar explores a major area of development from the last decade. Presented by Richard Young, it covers:

- The changing regulatory environment for medical devices in Europe 
- FDA regulation 
- Key considerations in development environments 
- Key standards 

ISO 13485:2016 – An Overview of General and Product Realisation Requirements

Led by Richard Young, trainer for MDTI's 'Advanced Regulatory Affairs for IVDs' and 'Practical Guidance for Medical Device Audits and Inspections' courses, this c. 20 minute webinar covers:

- Impacts of the new revision
- New terminology
- General requirements
- Resource management
- Product realisation and design controls
- Q&A session

Clinical evaluations, incorporating biological evaluation and PMCF with Sam Martin

In c.30 minutes, gain an overview of clinical evaluation and how it interacts with biological evaluations and post marketing clinical follow-up. Webinar highlights include:

  • Introduction to clinical evaluations
  • Discover how to incorporate biological evaluations into the clinical evaluation
  • Examine best practices to combine PMCF data into the clinical evaluation

To find out more about one of our training courses on this topic, please visit our course website.

Future European Regulation of In Vitro Classification

Led by Richard Young this high level 30 minute webinar will provide you with valuable updates and insights into the classification system proposed in the new IVD Regulation. You will gain solid grounding in the new risk based approach to classification so you can begin to evaluate your diagnostic products and prepare for the future changes.

  • Regulatory update and impact on the IVD industry
  • Outline of changes to classification: A risk based approach
  • Reviewing Annex VII: Rule 1- 8

To find out more about one of our training courses on this topic, please visit our course website.

Webinar Topic Suggestions

Please feel free to contact us with any ideas for future webinar topics.

Please email Roisin Manning ( Webinar ideas are subject to approval and appropriate trainer availability.