Approval of IVDs (in vitro diagnostic medical devices) in the EU

In vitro diagnostic medical devices (IVDs) are medical devices used to analyze samples derived from the human body. Typically, these products are reagents, kits, instruments, and devices. Software can also be considered as an IVD regarding its intended purpose. When “approving IVDs,” manufacturers must comply with many regulations, laws, and standards. 1. Significant steps for…

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Classification of in-vitro diagnostic medical devices: how to avoid a too-high classification

The classification of in-vitro diagnostics (IVD) can have far-reaching consequences, as it has an impact on the conformity assessment procedure, certification audits, and, thus, on market launch. To ensure that your IVD product is not unnecessarily allocated to a high-risk class, this article provides an overview of 1. What qualifies a product as an IVD?…

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