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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

8 - 10 March 2021

Thank you for attending MedTech Digital Week 2021

Featured

MedTech: EU MDR Exchange

15 - 17 June 2021, Delivered in CEST time zone

The EU MDR: Need Answers?

Software as a Medical Device Digital Week

26 - 27 April 2021

Explore The Latest updates to Software Regulations for Medical Devices from the European Commission and Notified Bodies

MedTech Summit

18 - 22 October 2021, Dublin

EU MDR, IVDR & Global Market Regulations: Bringing The Latest Guidance To You

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

Training

Showing 4 of 14 coursesView all courses

Regulatory Affairs in Latin America for Medical Devices

28-29 April 2021, Delivered over 2 days

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

LLM Medical Law and Ethics

27 September 2021, 27 Months

Analyse, interpret and apply the laws regulating the provision of healthcare with particular regard to ethical perspectives

Medical Device School

TBC, 3 days

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

Health Apps and Medical Device Software in Europe

TBC, 2 days

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

Articles & Video

Showing 9 of 43 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.

Clinical expectations of the EU MDR with TÜV SÜD and MedSmart

Clinical expectations of the EU MD: Matthias Fink from TÜV SÜD, and Dona Occhipinti from MedSmart discuss in this exclusive video interview.

EU MDR

The Journey to EU MDR Implementation - MedTech eBook Series

We answer some of the questions around EU MDR implementation in this MedTech Series eBook.

Medical Device

How the changing EUDAMED timeline impacts implementation of the EU MDR - with Eudamed.eu CEO Richard Houlihan

Diversity and Inclusion

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

Changes to the ISO 10993-23 and its impact on the medical device industry with NAMSA

MedTech

EU Notified Body Association Takes Steps to Allay EC's Virtual Audit Fears

EU MDR & IVDR

MDR and IVDR: Onsite or offsite audits? That’s the question.

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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