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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 6 of 7 eventsView all events
Featured

MedTech Digital Week

17 - 18 October 2023

Explore The Latest EU MDR Insights, Tools And Guidance With This Complimentary 3-Day Webcast Series. Register Now To Watch On-Demand.

Featured

MedTech: EU MDR Exchange

15 - 17 June 2021
, Delivered in CEST time zone
Thank you for attending MedTech: EU MDR Exchange 2021!

MedTech Summit US

November 14 - 16, 2023
, Minneapolis, Minnesota

Global Medical Device and Biocompatibility Regulatory Updates: Accelerate Market Access & Achieve Compliance

MedTech Summit

10 - 14 June 2024
, Brussels, Belgium (Hybrid Event)

The Flagship Regulatory Event for the Medical Device and In Vitro Diagnostic Industry

Transparency, Aggregate Spend & HCP Engagement 2024

Delivered as a Hybrid Event August 13-15, 2024
, McLean, VA

Forward-Thinking Strategies and Practical Implementation to Ensure Compliance, Manage Risk and Drive End-to-End Business Decisions.

MedTech Series

Year Round Events And Content

Your Central Knowledge Hub For MedTech Regulation, Strategy And Compliance

Courses

Showing 4 of 7 coursesView all courses

Understanding Labelling and UDI for Medical Devices and IVDs

Starting 3-4 October 2023
, Delivered over 2 days | 9am - 5pm CEST

Consolidate your strategies for labelling and UDI compliance under the EU MDR and IVDR

Introduction to Biocompatibility

Starting 22 - 23 February 2023

Understand the fundamentals of Biocompatibility and gain confidence in adhering to global standards

IVD School

28 - 30 March 2023
, Delivered in CET Timezone

IVD School: A comprehensive guide of the full in-vitro diagnostic industry

Health Apps and Medical Device Software in Europe

Starting 12 - 13 June 2023
, Delivered over 2 days | 8am - 4pm BST

Capitalise on the opportunities of medical device software under the EU MDR and accelerate your market success

Articles & Video

Showing 8 of 51 articles & videoView all articles & video
Featured
EU MDR

Data Report: Implementation of EU MDR

This MedTech Series report looks at post-EU MDR implementation data based on analysis of of a research study across medical device professionals.
MedTech

Implementation of EU MDR | MedTech Series eBook

Following the implementation of the EU MDR in May 2021, this MedTech Series eBook answers a number of questions organizations are still struggling with.
COVID-19

REPORT: COVID-19 One Year On - Impacts on the Global Life Sciences Industry 2021

EU IVDR

REPORT: EU IVDR State of the Industry 2021

COVID-19

Life Sciences Survey: COVID-19 Impacts One Year On

IVDR

Survey: EU IVDR State of the Industry 2021

PRRC

Your Questions Answered: Understanding the role of Person Responsible for Regulatory Compliance

Diversity and Inclusion

REPORT: Diversity, Equity and Inclusion in the Life Sciences 2021

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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