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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

8 - 10 March 2021

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

20 - 24 June 2022, Live In-Person Event: 20-24 June 2022, Dublin, Ireland

Thank you for attending MedTech Summit 2021

Biocompatibility for Medical Devices US

More details soon

Navigate the evolving biocompatibility landscape for medical devices

MedTech Series

Year Round Events And Content

Your Central Knowledge Hub For MedTech Regulation, Strategy And Compliance

MedTech Summit US

Dates TBC, Philadelphia, PA

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

Training

Showing 4 of 15 coursesView all courses

Medical Device School

7-9 December 2021

Gain a practical overview of the processes involved in bringing a medical device to market led by an expert faculty

Regulatory Affairs in Latin America for Medical Devices

23 - 24 February 2022, Delivered over 2 days

Develop your understanding of the regulatory landscape in Latin America to ensure fast device registration

Health Apps and Medical Device Software in Europe

1 - 2 September 2021, Delivered over 2 days | 9am - 5pm BST

Learn how to choose the optimal route to market your software under the Medical Device Regulation

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

16-17 November 2021, Delivered over 2 days | 9:00am - 5pm GMT

Navigate The New EU IVD Regulation For Successful Product Approval

Articles & Video

Showing 9 of 51 articles & videoView all articles & video
Featured
MedTech eBook Series

The EU MDR Delay and Implementation - MedTech eBook Series

Discover the challenges of EU MDR implementation and impacts of the delay on the medical device industry in this MedTech eBook.

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.

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

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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