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THE IQVIA INSTITUTE

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"Digital Health Trends 2024 - Implications for Research and Patient Care

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"DCTs Deliver Big ROI

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"Capturing value at scale: The $4 billion RWE imperative

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Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.

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IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.

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Brochure
IVDR Essentials: How to adapt to the upcoming IVDR
Understand the key changes of the IVDR and build a strategy and plan for IVDs to comply with the new requirements
Oct 11, 2021
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  • IVDR Essentials: How to adapt to the upcoming IVDR
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The transition to the new In vitro diagnostic regulation (IVDR) will require adopting a life-cycle approach. The purpose of the IVDR is to ensure that all in vitro diagnostic (IVD) medical devices used in the EU are compliant, therefore medical device and diagnostic companies will need to develop a strategy and plan to effectively for obtaining CE mark for IVD devices. This brochure offers guidance on how to build an IVDR strategy and breaks down the key changes from the directive to the regulation, as well as essential information of the IVDR.

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