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How to Get More Mileage Out of Your Electronic IFU

March 11, 2020

European Medical Device Regulation (EU MDR) will require medical device manufacturers to create electronic instructions for use (eIFUs). To meet this requirement, it’s common for manufacturers to convert their IFU to a pdf and upload it to a website. But this practice oversimplifies the eIFU and overlooks it as a rich source of data and information—not just for EU MDR, but also FDA regulatory compliance, and more.

Read the full MedTech Intelligence article here.