Bringing you the latest updates on competition law, patent litigation, regulatory frameworks, compliance and licensing agreements for Medical Devices and Diagnostics.
Articles & Video
MDR and IVDR: Onsite or offsite audits? That’s the question.
We examine the latest requirements with regard to Notified Bodies’ audits performed in the context of quality management system (QMS) assessment.
EU Pharmaceutical Law Forum 2020: Post-event Report
We review key session highlights from the virtual EU Pharmaceutical Law Forum.
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.
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.
COVID-19 Report: The Response to and Impacts on the Global Life Sciences Industry
COVID-19 Report: How is the life sciences industry developing a vaccine, treatment and testing for COVID-19 and what impact is it having on supply chain?
Pharma and Medical Device Regulations Content Library: Whitepapers and Reports Collection
Explore our collection of exclusive whitepapers and reports covering the hottest topics in pharma, biotech and medical device regulatory affairs and law with one simple registration.
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.
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.
Understanding how ISO 10993-17 and ISO 10993-18 connect - WHITEPAPER
This whitepaper explores parts 17 and 18 of ISO 10993, how they relate, and considerations for industry.
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.