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12-16 October 2020|Clayton Hotel Burlington Road,Dublin

EU MDR & IVDR: 2 Years To Go. 2 Regulations To Meet. Are you ready?

Navigate EU And Global Regulations For Medical Devices, IVDs And Combination Products With Dedicated Coverage Of PMS & Vigilance, Clinical Strategies, Software, Law and Sterilisation

NEW FOR 2020: Software & AI and Biocompatibility. Plus Clinical Data Management Training

MedTech Summit Has Been Rescheduled

Due to the increasing travel restrictions from developments with COVID-19 and feedback from key stakeholders, MedTech Summit 2020 has been postponed.

New Dates: 12-16 October 2020

New Venue: Clayton Hotel Burlington Road, Dublin

We’re genuinely disappointed to do this but the safety and experience of everyone involved is our top priority and we’re committed to following the guidance of the local authorities.

We thank you all for your understanding and look forward to seeing you in October.

Registered Attendees: Your registration will automatically carry over to the new dates and you do not need to re-register. Should you have any questions, please contact our customer service team at 

Fast-Track Your Compliance Strategy With Leading Industry Insights

Select your MedTech interest areas below to discover what we have lined up for you...

EU Medical Device Regulation

EU MDR: The Deadline Is Approaching. Are you Ready?

Find out more
Post Market Surveillance & Vigilance

Don’t Fall At The PMS Hurdle: The EU MDR Date Of Application Is In Sight

Find out more
Clinical Evaluations & Investigations

Take Your Clinical Evaluation & Investigation Strategies To EU Levels

Find out more
EU IVD Regulation & Strategy

EU IVDR: We're Half Way There…

Find out more
EU Medical Device Law

Master The Legal Implications Of The EU MDR With Leading Insights, Case Studies And Interactive Discussions

Find out more
Software & AI

Break Through The Regulatory Hurdles. The Future Of Medtech Is Here…

Find out more
Medical Device Regulatory Affairs in Global Markets

Think Global: Advance Your Medical Devices To New Regions With Leading Regulatory Knowledge And Know How

Find out more
Drug Device Combination Products

Navigate The Regulatory Landscape For Drug Device Combination Products Under The EU MDR

Find out more
Sterilisation and Reprocessing of Medical Devices

Achieve Best Practice Medical Device Sterilisation And Reprocessing With Leading Industry Insights

Find out more
Biocompatibility for Medical Devices

ISO 10993: Take Your Biocompatibility Testing To New Levels With Practical Advice From ISO TC 194, Competent Authority, Notified Body And Industry Experts

Find out more
TRAINING COURSE: Medical Device Regulatory Project Management

Gain A Solid Understanding Of The Core Ingredients Needed For Successful Regulatory Project Management

Find out more
TRAINING COURSE: US Regulatory Affairs for Medical Devices

Get A Comprehensive Foundation In US Regulatory Affairs To Make Your Submission A Success

Find out more
TRAINING COURSE: Medical Device Clinical Data Management

Get To Grips With How Best To Manage, Store And Process Your Medical Device Clinical Data

Find out more

MedTech Summit At A Glance

Gain full access to all conference tracks on the days you attend

Explore the online agenda for more information on the topics being presented:

Strive For Regulatory Compliance With:

Medtech Professionals
Competent Authority & Notified Body Representatives
Medical Device, Diagnostic & Combination Product Companies Represented


EU MDR: Update on the delay and impact on industry

With confirmation of the EU MDR delay due to COVID-19, MedTech Summit brought together four industry insiders to discuss the update and the impacts it will have on industry, featuring:

  • Gert Bos,  Executive Director & Partner at Qserve Group, The Netherlands
  • Annabelle Bruydonckx, Counsel at Simmons & Simmons LLP, Belgium
  • James Whitehead,  Patient Safety Medical Device Lead at AstraZeneca, UK
  • Vladimir Murovec, Supervising Associate (Healthcare & Life Sciences) at Simmons & Simmons, Belgium

Rebecca Brady, Senior Conference Producer at Informa Connect Life Sciences, led the discussion. Watch it now to hear their leading perspectives on the EU MDR delay.

Introducing The MedTech Summit 2020 Advisory Board

Basira Salehi, Senior Manager Clinical Science & Medical Affairs, Biotronik, Switzerland

Gert Bos PhD, Executive Director & Partner, Qserve, Netherlands

Heather Taylor, Director of Marketing, NSF International, Belgium

Koen Cobbaert, Senior Manager - Quality, Standards & Regulations, COCIR, Belgium

Sabina Hoekstra, Regulatory Affairs Expert, Netherlands 

Collect CPD Points At The MedTech Summit

2 Day Pass = 10 CPD Points
3 Day Pass = 15 CPD Points
4 Day Pass = 20 CPD Points
5 Day Pass = 25 CPD Points

MedTech Summit Caught On Camera

Watch our short highlights video to see why the medtech industry's leading regulatory experts attend...

Event Partner: MedTech Insight

Global medical technology news & analysis from trusted experts

Medtech Insight offers real-time and extensive coverage on the global medical technology market with access to the latest news and insight on medical technology regulatory, product and company developments, tracking expert opinions, investment trends, deals, and shifts in industry dynamics. Discover how to uncover medtech opportunities in a continuously evolving market.

Visit to find out more.

MedTech Videos, Articles And Reports

Watch our MedTech TV Video Interviews filmed live at the 2019 event.

Read whitepapers and articles to stay up to date with the latest medtech news.

Discover the latest trends across the industry with our medtech industry reports.

Connect With Key Buyers At MedTech Summit 2020 In Dublin

Whether you're increasing your company profile, launching a new product or focusing on new business development opportunities, collaborate with us to identify custom solutions to help you reach your goals.  

Contact Linda Cole: | +44 (0) 20 7017 6631


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