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Regulatory Affairs, Medical Devices

Notified Body designation and scope, the impact of Brexit and Competent Authority and Notified Body interpretation of the regulations. Make sure you are up to date!

Events

Showing 4 of 4 events

MedTech Summit

22 - 26 June 2020, Dublin

EU MDR & IVDR: The End Is In Sight

Biocompatibility for Medical Devices

3-4 November 2020, Amsterdam, The Netherlands

Thank you to all who made this year's event a huge success! Stay tuned for 2020 updates.

MedTech Summit US

December 1-3, 2020, Philadelphia, PA

THANK YOU TO EVERYONE WHO ATTENDED THE 2019 MEDTECH SUMMIT US!

Biocompatibility for Medical Devices US

October 24 - 25, 2019, Chicago, IL

Navigate the evolving biocompatibility landscape for medical devices

Training

Showing 4 of 24 coursesView all courses

Fundamentals of the EU IVD Regulation

Starting 2 Mar 2020, 5 weeks online

Decode the new European IVD regulation - Understand the key areas of impact for IVDs within the new regulatory requirements

Fundamentals of Medical Device Risk Management

Starting 1 Jun 2020, 4 weeks online

Get to grips with the latest risk management requirements - Improve your understanding of the latest risk requirements and responsibilities outlined in the MDR

Fundamentals of Biocompatibilty

Starting 6 Jul 2020, 4 weeks online

Familiarise yourself with the updates to ISO 10993-1

Understanding The European IVD Regulation

13 - 14 Oct 2020, London

Examine the new IVD Regulation to understand how the changes will impact you as a manufacturer throughout the lifecycle of your products

Articles & Video

Showing 9 of 9 articles & video
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LSP Article

Comparing EU and FDA approaches to regulating MedTech software and AI - WHITEPAPER

This whitepaper explores the different EU and FDA approaches to regulating MedTech software and AI.

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MedTech

EU MDR: New expectations for clinical evaluations and investigations - WHITEPAPER

In May 2020 the EU MDR officially replaces the EU MDD. This whitepaper assesses new expectations for clinical evaluations and investigations under the EU MDR.

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EU MDR

EU MDR: Assessing the impact on biocompatibility testing

This whitepaper examines the regulatory changes brought by the EU MDR around medical device biocompatibility testing, and how compliance will affect common practice.

MedTech TV

MedTech TV: EU MDR and IVDR implementation challenges

At MedTech Summit in Brussels we interviewed two industry insiders on the hottest topics facing the industry for MedTech TV - watch the full interviews here.

Biotech Showcase™ 2020

What's shaping the future of biotech?

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Regulation

Understanding how ISO 10993-17 and ISO 10993-18 connect - WHITEPAPER

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ESubmissions

Regulatory development opportunities for global harmonisation of eSubmissions

MedTech

MedTech 2020 Survey: EU MDR and IVDR Compliance

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LSP Article

MedTech Report: State of the Industry 2019

SPONSORSHIP & EXHIBITION OPPORTUNITIES

Let us help you engage qualified decision makers in need of experts and services to ensure compliant medical device products. Share your strategy and plans so we can help you identify the best opportunities to reach your objectives. Our team will collaborate with you to develop a bespoke program tailored to your unique needs.

To find out more about sponsor opportunities, contact Linda Cole:
linda.cole@informa.com | +44 207 017 6631

Download Medtech Sponsor Prospectus

All opportunities can be customised to align with your needs and budget. Examples may include:

  • Exhibition space
  • Speaking slots and onsite video interviews
  • High-impact branding and messaging
  • Private/public hosted events (lunches, breakfasts, and receptions)
  • Custom digital campaigns

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