The European Commission is seeking feedback on its draft Implementing Regulation on electronic instructions for use (eIFU) of medical devices. The proposal expands the use of digital instructions to all medical devices for professional users, aligning with the healthcare sector’s push for efficiency, accessibility, and sustainability.
The European Commission is accepting open feedback (max. 4000 characters) with no structured questionnaire: a unique opportunity to provide direct input, sharing real-life experiences, concerns, and recommendations regarding the transition to eIFU.
Make your voice heard! Submit your feedback by 21 March 2024 here.