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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 8 eventsView all events
Featured

MedTech Digital Week

3 - 5 October 2022

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

December 6 - 8, 2022, Chicago, IL

Medical Device Regulations Across the Globe: Your Dedicated Hub To Achieving Compliance

MedTech Summit

19 - 23 June 2023, Brussels, Belgium

MEDTECH SUMMIT 2022: THE FLAGSHIP REGULATORY EVENT OF THE YEAR

Transparency, Aggregate Spend & HCP Engagement 2023

Delivered as a Hybrid Event August 8-10, 2023

Unrivaled industry authorities lay the groundwork to transcend compliant transparency programs across the business.

Biocompatibility for Medical Devices US

More details soon

Navigate the evolving biocompatibility landscape for medical devices

Training

Showing 4 of 17 coursesView all courses

Regulatory Affairs for IVDs with a focus on the new IVD Regulation

2023 Dates Coming Soon, Delivered over 2 days | 9:00am - 5pm GMT

Navigate the highly regulated IVD industry and ensure market access for your device

Medical Devices in the APAC Region

2023 Dates Coming Soon!, 2023 Dates Coming Soon!

Analyse and navigate the complex requirements of medical device regulation and submission for the APAC region

Health Apps and Medical Device Software in Europe

30 - 31 May 2022, Delivered over 2 days | 8am - 4pm BST

Examine the go-to market challenges and opportunities for medical device software under the EU MDR

Regulatory Affairs in Latin America for Medical Devices

28 - 29 June 2022, Delivered over 2 days

Navigate The Medical Device Regulatory Landscape In Latin America For Faster Approvals

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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