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Compliance & Legal, Medical Devices & Diagnostics

Bringing you the latest updates on competition law, patent litigation, regulatory frameworks, compliance and licensing agreements for Medical Devices and Diagnostics.

Articles & Video

Showing 12 of 12 articles & video
EU Pharmaceutical Law

EU Pharmaceutical Law Forum 2020: Post-event Report

We review key session highlights from the virtual EU Pharmaceutical Law Forum.
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

报告:医疗COVID-19后的未来

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

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?
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Regulatory affairs

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.
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MedTech

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.
Survey

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.
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Regulation

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.
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LSP Article

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

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.
LSP Article

EU Pharmaceutical Law Industry Report 2019

Download our exclusive EU Pharmaceutical Law Report, exploring the state of the industry in 2019.

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