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.
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.
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.
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.
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.
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.
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.
Life Sciences in 2030 Survey: Complete to win a 2-day conference pass
We are a conducting a huge survey of life sciences professionals around the world on how the industry will look by 2030. Complete it here to get early access to the final report.
Regulatory challenges for Software as Medical Device (SaMD) and AI
We asked six medical device industry experts about the regulatory challenges of Software as Medical Device (SaMD) and Artificial Intelligence.
EU MDR: New expectations for clinical evaluations and investigations - WHITEPAPER
In May 2020 the EU MDR officially replaces the EU MDD. This whitepaper assesses new expectations for clinical evaluations and investigations under the EU MDR.
Comparing EU and FDA approaches to regulating MedTech software and AI - WHITEPAPER
This whitepaper explores the different EU and FDA approaches to regulating MedTech software and AI.
MedTech 2020 Survey: EU MDR and IVDR Compliance
Complete our MedTech survey on EU MDR and IVDR Compliance to be in with a chance of winning a 2 day conference pass to MedTech Summit.