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MedTech: EU MDR Virtual Conference Features & Benefits

Engage. Exchange. Collaborate.

A Brand New Focused Virtual Opportunity To Learn From Medical Device Professionals Working Towards EU MDR Compliance From All Around The Globe

Watch The Virtual Platform Demo Video For MedTech: EU MDR Exchange


At a time of vast regulatory change, it is more important than ever for the medtech community to stay connected, discuss implementation and share practical learnings.

Through our sophisticated and fully interactive virtual platform, you will be able to engage with fellow industry professionals facing similar challenges, hear from those shaping the regulatory landscape, and gather the information and contacts you need to take the next steps towards achieving and maintaining EU MDR compliance.

Watch our short demo video to see what the virtual conference platform will look like...

Work Around Your Schedule With Live And On-Demand Access

Attend presentations live to ask questions to the speakers and panels for real-time feedback.

And, benefit from on-demand* viewing access for 30 days post-event, giving you the opportunity to catch up on sessions you missed while attending other talks within the live agenda, or meeting with colleagues!

*Excluding sessions limited to live viewings only. Subject to speaker permissions.



Stay At The Forefront Of EU MDR, Clinical & PMS Discussion With 7 New And Improved Interactive Virtual Formats


Interview
Interview

Join us for a 25-minute interview with Richard Houlihan, CEO,  EUDAMED, addressing the timelines for the uncompleted modules of EUDAMED, data requirements in the absence of EUDAMED modules, how much data manufactures need to hold to be compliant and more.

Flash Sessions
Flash Sessions

Benchmark with real-world examples of class I, II and III device submissions in these fast and focused 15 minute presentations followed by live Q&A panels.

Live Panel Discussions
Live Panel Discussions

Put your questions forward in live panel Q&As on topical matters including; First Experiences with EU MDR Submissions; Meeting Clinical Evaluation Requirements; Meeting PMS Requirements; and Benefit vs Risk.



Dual Dialogues
Dual Dialogues

Including a keynote session sharing experiences on a specific product's submission journey from the perspective of the Notified Body and manufacturer, with TÜV SÜD America and BD and MedSmart

Roundtables
Roundtables

Join focused virtual roundtable discussions on first experiences of Economic Operators under the EU MDR, and Annex 16 under the EU MDR, starting with a short presentation introducing the topic and opening up the discussion to the floor.

Tech Tours
Tech Tours

Learn about the latest products, services technologies and solutions in the EU MDR space in these short and informative video demonstrations.


25 minute presentations followed by live Q&A
25 minute presentations followed by live Q&A

Providing you with ample opportunity to learn and put your questions forward for tailored feedback.

Virtual Networking Made Easy

The virtual event platform provides access to the full attendee list, making it easy to identify individuals and connect with professionals that are most relevant to you, helping you have the conversations that matter.

Networking opportunities include:

  • Share questions and ideas throughout the agenda in a whole host of interactive sessions.
  • Exchange instant web messages with fellow participants.
  • Schedule 1:1 video meetings.


Who should attend MedTech: EU MDR Exchange

All medical device professionals with work relating to the EU MDR will benefit from attending this event, including those who have responsibilities or involvement in the following areas:



  • Regulatory Affairs
  • Quality Assurance/QA
  • Quality Manager
  • Regulatory Compliance
  • Compliance
  • Government Affairs
  • Regulatory Intelligence
  • MDR Project / Programme Management
  • EU MDR Implementation
  • Regulatory Policy Lead
  • Global Regulatory Affairs
  • Post Market Surveillance
  • Vigilance
  • Risk Management
  • Device Management
  • Adverse Event Reporting
  • Medical Safety
  • Complaints Management
  • Strategy Management
  • Quality Systems
  • Quality Engineer
  • Trend Management / Reporting
  • Clinical Evaluations
  • Clinical Science
  • Clinical Affairs
  • Clinical Research
  • Clinical Practice
  • Clinical Development
  • Clinical Manager
  • Clinical Safety
  • Clinical Strategy
  • Clinical Risk Management
  • Clinical Specialist
  • Clinical Project Management
  • Clinical Programme Management
  • Clinical Assessor
  • Clinical Analyst
  • Medical Writer
  • Certification
  • Inspector
  • Auditor
  • Legal Partner / Counsel

ENERGY SAVING TIPS

Here are some useful tips to reduce your energy usage throughout the virtual event:

  • Reducing your screen brightness from 100% to 70% is hardly noticeable and can reduce energy consumption by 20%.
  • Reducing cooling by 1°C can reduce energy use by up to 8%.
  • Switch to energy saving mode on your computer or screen, or sit in areas with natural light.