Electronic instructions for use for medical devices
EU Regulation 2017/745 (MDR) establishes the general requirements for instructions for use (IFU). Whether they can also be provided in electronic form (eIFU) is regulated by Implementing Regulation (EU) 2021/2226. It was revised by Implementing Regulation (EU) 2025/1234. An official consolidated version is not available, so both regulations must always be read in combination. We have summarized the requirements…
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