This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Browse our events, training, articles and people by topicclose

Popular sectors

A - Z

Browse Topicsappsclose
search

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!

Articles & Video

Showing 21 of 36 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

Explore our exclusive report on the EU IVDR State of the Industry 2021 based on over 100 survey responses.
COVID-19

Life Sciences Survey: COVID-19 Impacts One Year On

Take part in our industry survey on the impacts of COVID-19 on the life sciences one year on to get exclusive early access to the final report.
IVDR

Survey: EU IVDR State of the Industry 2021

EU IVDR State of the Industry: Take part in our survey to get exclusive early access to the final report.
PRRC

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

The TEAM-PRRC EU Association answer your questions on understanding the role of Person Responsible for Regulatory Compliance (PRRC) under the EU MDR.
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

Richard Houlihan, CEO of EUDAMED.EU, discussed the EUDAMED modules status and the impact on implementing the EU MDR in this exclusive interview.
Diversity and Inclusion

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

Complete our survey on Diversity, Equity and Inclusion in the Life Sciences 2021 to get exclusive early access to the final report.
MedTech

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

Amanda Maxwell looks at how the EU Notified Body Association is helping allay virtual audit fears.
MedTech

REPORT: Adoption of AI and Digital Solutions in the MedTech Industry

This exclusive report looks at how AI and digital solutions have been adopted in the MedTech industry, and what the future looks like.
MedTech Summit

MedTech Summit 2020 Post-Event Report

Find the latest on EU MDR, IVDR and medical device law in this MedTech Summit 2020 Post-Event Report.
Survey

Survey: Adoption of AI and Digital Solutions in the MedTech Industry

Take part in our study to discover the adoption of AI and digital solutions in the MedTech industry.
MedTech eBook Series

Clinical Evaluations for Medical Devices and IVDs - MedTech eBook Series

Discover how the EU MDR will affect clinical evaluations for medical devices and IVDs in this MedTech Summit eBook.
COVID-19

Report: Partnering And Deal-Making in Pharma through the Pandemic

This Informa report explores how partnering and deal-making in the pharma industry has been impacted by COVID-19.
Healthcare

REPORT: The Future of Healthcare Post COVID-19

In our latest report learn how healthcare organizations are adapting to succeed post COVID-19, from innovation to product development.
Regulatory affairs

Barriers and Challenges for Global Regulatory Harmonization

What obstacles are keeping regions such as Latin America from achieving regulatory harmonization with the rest of the world?
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.
Diversity

REPORT: Diversity, Inclusion and Sustainability in the Global Life Sciences Industry 2020

Diversity and Inclusion in Life Sciences 2020: Research analysis of how life sciences professionals around the world view representation of women and minorities in the industry, plus the importance of sustainability.
EU MDR

MedTech Digital Week 2020 agenda revealed

We reveal the full agenda of the 3-day webinar series providing EU MDR and IVDR updates and practical insights for implementation.

Copyright © 2023 Informa Connect Limited. Registered in England & Wales with number 01835199, registered office 5 Howick Place, London, SW1P 1WG.