Bringing you the latest updates on competition law, patent litigation, regulatory frameworks, compliance and licensing agreements for Medical Devices and Diagnostics.
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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.
REPORT: Diversity, Equity and Inclusion in the Life Sciences 2021
Explore the Diversity, Equity and Inclusion in the Life Sciences 2021 report based on an exclusive study of 483 industry professionals.
COVID-19 and Compliance Teams in Life Science Industry: 2021 Survey Report
After the tumultuous year that 2020 was,
we invited responses for our “COVID-19
and Compliance Teams in Life
Sciences Industry” survey to gauge
the impact of the COVID pandemic on
compliance departments across life
The survey was divided to record
responses with respect to compliance
teams size, budgets, use of counsel,
mode of monitoring and training.
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.
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.