The European Commission has today disclosed implementing measures rolling plan under the MDR and IVDR. The document gives a bit more clarity on the timeline for the adoption of future Implementing Acts and other measures under the new Regulations.
In November 2019, we can expect the publication of three Implementing Acts addressing:
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Reprocessing of single-use medical devices
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Common specifications for products without a medical purpose
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Setting up of expert panels
Here, you can find the full list of Implementing Acts and measures to be adopted in the next two upcoming years.
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