Resources

EU MDR: Compliance Requirements From a Vigilance Perspective

Companies attempting to comply with Medical Device Regulation (EU) 2017/745 (MDR), introduced in May 2021 for medical device certification in the EU are challenged by the complexity and scope of the requirements. It is important for medical device...

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1 min read

ICER Set to Evaluate Non-Drug Products in 2020

The Boston-based Institute for Clinical and Economic Review (ICER), an independent research organization that conducts health technology assessments...

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1 min read

Possibility for Examination to be Included in the SHI Fee Scale Brings More Certainty for Reimbursement for New Diagnostics in Germany

Manufacturers can now have more certainty about the process of inclusion of a new laboratory, new human-genetic, or new tumor-genetic diagnostics in...

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6 min read

Preclinical Insights #39 — 25 Years of Preclinical Paris: A Conversation with Our Founders

Veranex is proud to share the latest issue of our Preclinical Insights publication. In this issue we talk with Preclinical Paris Founders Nicolas...

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Leveraging Medtech Innovation in Clinical Trials

Rebecca Ford, Director of Program Management, discusses how to Leverage medical technology and innovation in clinical trials to drive medication...

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2 min read

Event Recap: Biocompatibility Insights 2023

This year’s Biocompatibility Insights conference took place in Annapolis, MD, US from September 25–27, 2023. The framework for the event was...

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TRI-CON 2024

Precision Med TRI-CON March 26-28, 2024 Hilton San Diego Bayfront, San Diego, CA and Virtual Register Now to join us in San Diego for networking, and...

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