Quite Recently, The European Commission published the timeline of when this system will be in place, functional and enforced for mandatory use.
Want to Know More about EUDAMED?
Source of the Timeline - https://health.ec.europa.eu/system/files/2022-07/md_eudamed_timeline_en.pdf
In October 2023, EUDAMED got a new time line
According to this roadmap, EUDAMED will be a Mandatory tool for all Medical Device products by Q4 2027 and will have an 18-month transition period.
As the Regulatory Tools design and develop, Manufacturers need to focus on compliance with the requirements. Our Experts are here to cut through the regulatory maze and be your Regulatory Risk Partners for Medical Devices, Diagnostics and Digital Health!
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