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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 Biocompatibilty

Starting 3 Feb 2020, 4 weeks online

Familiarise yourself with the updates to ISO 10993-1

Advanced Regulatory Affairs For Medical Devices

5 - 6 Feb 2020, London

Develop improved tactics to ensure the effective life-cycle management of your product

Health Apps and Medical Device Software in Europe

13 - 14 Mar 2020, London

Through scene-setting introductions and highlighted case extracts, decode the practical implications of the legislation surrounding all software devices

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 8 of 10 articles & videoView all articles & video
Featured
MedTech

MedTech 2020 Survey: EU MDR and IVDR Compliance

Complete our MedTech survey on EU MDR and IVDR Compliance to be in with a chance of winning a 2 day conference pass to MedTech Summit.

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Global Pharmaceutical Regulatory Affairs State of the Industry Report 2019

In early 2019, we surveyed the perspectives of pharmaceutical regulatory professionals around the world. This report reveals insights into the industry's greatest challenges.

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Regulations

China's changing pharmaceutical regulatory approval landscape

China has recently taken unprecedented steps to improve its healthcare and regulatory system. This whitepaper examines the recent changes and what opportunities and challenges they bring.

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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LSP Article

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

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ESubmissions

Regulatory development opportunities for global harmonisation of eSubmissions

Esubmissions

Global Pharmaceutical Regulatory Affairs: Tell us your view

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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