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ISO/DIS 24884

Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of delivery

General information

40.20     Oct 13, 2025

ISO

ISO/TC 212

International Standard

11.100.10  

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Scope

The proposed new standard provides guidelines on the conditions (means of delivery) and minimum required information which shall be physically delivered, when providing electronic instructions for use (eIFU) for in vitro diagnostic medical devices (IVDs).
Not in the scope of this standard: The content of the eIFU as it is covered by ISO 18113-1, -2, -3, -4, -5.
This document is applicable to the in vitro diagnostic manufacturers, the developer (investigators), and the users such as medical laboratories. It is also intended to be used by the organizations (e.g. regulatory authorities and conformity assessment bodies), which are responsible for assessing the performance and quality control.

Life cycle

NOW

PROJECT
ISO/DIS 24884
40.20 DIS ballot initiated: 12 weeks
Oct 13, 2025

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