Articles & Video
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.
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.
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.
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.
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.
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.
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.
The Journey to EU MDR Implementation - MedTech eBook Series
We answer some of the questions around EU MDR implementation in this MedTech Series eBook.
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.
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.
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 2020 Post-Event Report
Find the latest on EU MDR, IVDR and medical device law in this MedTech Summit 2020 Post-Event Report.
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.
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.
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.
The role of COVID-19 antibody testing for employers
How can widespread COVID-19 antibody testing help reopen offices and how close are we to achieving it?
Update on the EU MDR delay and impact on industry - Panel discussion
With confirmation of the EU MDR delay due to COVID-19, MedTech Summit brought together four industry insiders to discuss the update and the impacts it will have on industry.
Coronavirus Diaries: "We’re seeing each other as people with lives outside of work"
In this new weekly series, Caroline Byrd from Leica Biosystems offers an insight into how her work and the wider industry is being impacted by COVID-19.
Article 117: Preparing Drug Device Combination Product Manufacturers for the EU MDR - WHITEPAPER
Article 117 EU MDR: This whitepaper offers advice to prepare drug device combination product manufacturers for the new regulations.
Preparing your organisation for MDSAP: Australia, Canada, Japan, Brazil - WHITEPAPER
This whitepaper details how your organisation can prepare for the Medical Device Single Audit Program (MDSAP) in Australia, Canada, Japan and Brazil.
Manufacturing Incident Reports (MIR) under the EU MDR - WHITEPAPER
This whitepaper explores Manufacturing Incident Reports (MIR) for medical devices under the EU MDR.