Search Tag: eIFU
2024 02 Feb
Medical Device Regulation (MDR) requires manufacturers to provide detailed instructions for use (IFU) to guide proper and safe use of medical devices and products. Regulation (EU) 2021/2226 (eIFU Regulation) establishes the conditions under which instructions for use may be provided in electronic form only. Although the eIFU Regulation acknowledges...Read more
2024 02 Feb
Medical Device Regulation (MDR) requires manufacturers to provide detailed instructions for use (IFU) to guide proper and safe use of medical devices and products. Regulation (EU) 2021/2226 (eIFU Regulation) establishes the conditions under which instructions for use may be provided in electronic form only. Although the eIFU Regulation acknowledges...Read more