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
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?
Post Market Surveillance & Vigilance
Don’t Fall At The PMS Hurdle: The EU MDR Date Of Application Is In Sight
Clinical Evaluations & Investigations
Take Your Clinical Evaluation & Investigation Strategies To EU Levels
EU IVD Regulation & Strategy
EU IVDR: We're Half Way There…
EU Medical Device Law
Master The Legal Implications Of The EU MDR With Leading Insights, Case Studies And Interactive Discussions
Software & AI
Break Through The Regulatory Hurdles. The Future Of Medtech Is Here…
Medical Device Regulatory Affairs in Global Markets
Think Global: Advance Your Medical Devices To New Regions With Leading Regulatory Knowledge And Know How
Drug Device Combination Products
Navigate The Regulatory Landscape For Drug Device Combination Products Under The EU MDR
Sterilisation and Reprocessing of Medical Devices
Achieve Best Practice Medical Device Sterilisation And Reprocessing With Leading Industry Insights
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
TRAINING COURSE: Medical Device Regulatory Project Management
Gain A Solid Understanding Of The Core Ingredients Needed For Successful Regulatory Project Management
TRAINING COURSE: US Regulatory Affairs for Medical Devices
Get A Comprehensive Foundation In US Regulatory Affairs To Make Your Submission A Success
MedTech Summit At A Glance
Strive For Regulatory Compliance With:
VIDEO PANEL DISCUSSION
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.
Industry Representatives Sharing Case Study Insights Include:
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 pharmaintelligence.informa.com/products-and-services/news-and-insights/medtech-insight to find out more.
MedTech Videos, Articles And 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: LCole@informaconnectls.com | +44 (0) 20 7017 6631
2019 Photo Gallery
Get a glimpse of the action...
Over 700 attendees from the medical device, diagnostics and combination product communities joined us in Brussels last year for the latest EU MDR, IVDR and Emerging Market Regulatory updates.
Over 5 days, the agenda included 20+ Competent Authority & Notified Body speakers alongside many industry speakers covering 9 crucial areas: EU MDR, IVDR, Post Market Surveillance and Vigilance, Clinical Evaluations and Investigations for Medical Devices, Clinical Outsourcing, Medical Device Law, Drug Device Combination Products, Regulatory Affairs in Emerging Markets, and Sterilisation & Reprocessing of Medical Devices.
Take a look at the gallery for a glimpse of the MedTech Summit 2019. And, if you attended last year, see if you can spot yourself...