17 - 21 June 2019
Crowne Plaza Brussels – Le Palace,
EU MDR & IVDR: The final countdown
Talking regulatory and clinical strategies, PMS & vigilance, legal, combination products, sterilisation and emerging market requirements
NEW FOR 2019: Clinical outsourcing PLUS 2 training courses
Regulatory Implementation: Navigating The Not So Yellow Brick Road To Compliance
EU Medical Device Regulation
Your one stop shop for EU MDR implementation advice
Clinical Evaluations & Investigations
Clinical strategies: Are you EU MDR compliant?
Post Market Surveillance & Vigilance
A helping hand to get you PMS & Vigilance ready
Your toolkit to ensure a smooth transition to the EU IVDR
Selecting partners and ensuring efficiency. All you need to know for outsourcing...
EU Medical Device Law
Navigate the legal ups and downs of the EU MDR: Strategic insights and practical advice
Medical Device Regulatory Affairs in Emerging Markets
Think Big: Strategic guidance for global regulatory success
Drug Device Combination Products
Tackle unique combination products challenges under the EU MDR: Classification, Implementation & Strategy
Sterilisation and Reprocessing of Medical Devices
The latest advice on sterilisation and reprocessing: Guidance, methods & process development
MDTI TRAINING COURSE: Medical Device Regulatory Project Management
Gain a solid understanding of the core ingredients needed for successful project management.
MDTI TRAINING COURSE: US Regulatory Affairs for Medical Devices
Get a comprehensive foundation in US regulatory affairs to make your submission a success.
The Summit At A Glance
Take a look at the online agenda to find out more about the individual sessions
Select your days and topics of interest to see what's on the line up for you...
Implement the EU MDR and IVDR with:
Gain Strategic Advice From Notified Bodies Including:
Benchmark Practical Implementation With Industry Case Studies From:
Webinars. Webinars. Webinars.
EU Medical Device Regulations, NB overview and update from BSI
James Newman, Technical Specialist, Scheme Manager & Training Lead – General Devices, BSI Group
WATCH THIS WEBINAR
Managing the transition to the IVDR
Richard Young, Managing Director, Acclaim Biomedical
WATCH THIS WEBINAR
High-Quality Real-World Clinical Data to Support Medical Device and Pharmaceutical Post-Mark Clinical Follow-ups
Dr. Vivian Tian, Business Development Manager – EU and US, 1MData
MedTech Report 2019: State Of The Industry
In February 2019, MedTech Summit conducted a survey of medical device and IVD professionals around the world. Based on 291 responses, this report reveals unique insights into the state of the industry today as we head towards the key 2020 and 2022 deadlines, the biggest challenges and how industry insiders are tackling them.
Download the full report to see what the general consensus is at present with regards to regulatory implementation challenges, expectations, areas of concern and more for Europe and beyond.
Collect CPD Points
Collect up to 25 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
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.
2018 Photo Gallery
Get a glimpse of the action...
Over 550 attendees from the medical device, diagnostics and combination product communities joined us in Brussels last year for all the latest EU MDR, IVDR and Emerging Market Regulatory updates. Over 5 days, the agenda included 25+ Competent Authority & Notified Body speakers alongside many industry speakers covering 8 crucial areas: EU MDR, IVDR, Post Market Surveillance and Vigilance, Clinical Evaluations and Investigations for Medical Devices, 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 2018. And, if you attended last year, see if you can spot yourself...
Sponsor or exhibit for 2019
To discuss how your company can get involved, please contact Linda Cole:
E: Linda.Cole@KNect365.com T: +44 (20) 7017 6631
Sponsor & Exhibitor testimonials:
"Good talks and great audience"
“This was the first time we attended and sponsored the event and we thought the agenda was spectacular. We were really impressed to see we had a full house when we presented. It was a 'no brainer' to sponsor this event – nothing like this exists in the US”
“Liked the interactive App which was very useful to see the session and not have to carry an event guide”
“Great meeting, very comprehensive and high level professional attendees”
MedTech Digital Week - Webinars On-Demand
On 3-6 December 2018 MedTech Digital Week, a 4-day series of topical webcasts and downloadable resources, brought together hundreds of medical device and diagnostics industry professionals for the latest Notified Body and industry insights on the EU Medical Device and IVD Regulations followed by live Q&As.
Watch the webinars on-demand now with representatives from BSI, Abbott, 1MData, Agfa Medical Imaging, PROSYSTEM - an NSF International Company and more.
Interested in sponsoring MedTech Digital Week 2019?
MedTech Digital Week is taking place on 28-31 October 2019. Request details to learn how you can promote your thought leaders at the next digital event.
Medical Device Training International | MDTI
MDTI is a global interactive training partner committed to the personal progression of Medtech professionals. We deliver CPD certified training on a wide range of topics including clinical evaluations, clinical investigations, regulatory affairs, combination products, PMS and vigilance, In Vitro Diagnostics (IVD)and soft skills. Our courses are delivered in a variety of formats such as public face-to-face, customised in-house, webinars, eBooks and online academies.