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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

12-16 October 2020, Dublin

EU MDR & IVDR: The End Is In Sight

Biocompatibility for Medical Devices

15-16 October 2020, Dublin

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

Biocompatibility for Medical Devices US

December 1 - 3, 2020, Philadelphia, PA

Navigate the evolving biocompatibility landscape for medical devices

MedTech Summit US

December 1-3, 2020, Philadelphia, PA

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

Training

Showing 4 of 24 coursesView all courses

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

Medical Devices in the MENA Region

Starting 6 Apr 2020, 4 weeks online

A comprehensive guide to local procedures, regulatory updates and best practice for obtaining successful approvals in the MENA region

Articles & Video

Showing 9 of 16 articles & videoView all articles & video
Premium
MedTech

MedTech Report 2020: EU MDR and IVDR Compliance

Download the MedTech Report 2020 on EU MDR and IVDR Compliance, based on 265 survey responses from industry insiders.

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MDSAP

Preparing your organisation for MDSAP: Australia, Canada, Japan, Brazil - WHITEPAPER

This whitepaper details how your organisation can prepare for the Medical Device Single Audit Program (MDSAP) in Australia, Canada, Japan and Brazil.

Coronavirus

Coronavirus Diaries: "We’re seeing each other as people with lives outside of work"

In this new weekly series, Caroline Byrd from Leica Biosystems offers an insight into how her work and the wider industry is being impacted by COVID-19.

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Medtech

Article 117: Preparing Drug Device Combination Product Manufacturers for the EU MDR - WHITEPAPER

Article 117 EU MDR: This whitepaper offers advice to prepare drug device combination product manufacturers for the new regulations.

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Manufacturing Incident Reports

Manufacturing Incident Reports (MIR) under the EU MDR - WHITEPAPER

Survey

Life Sciences in 2030 Survey: Complete to win a 2-day conference pass

Medical Device

Regulatory challenges for Software ​​​​​as Medical Device (SaMD) and AI

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EU MDR

EU MDR: Assessing the impact on biocompatibility testing

MedTech TV

MedTech TV: EU MDR and IVDR implementation challenges

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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