ISO/TS 82304-2:2021
Health software - Part 2: Health and wellness apps-Quality and reliability
This document provides quality requirements for health apps and defines a health app quality label in order to visualize the quality and reliability of health apps.This document is applicable to health apps, which are a special form of health software. It covers the entire life cycle of health apps.This document is intended for use by app manufacturers as well as app assessment organizations in order to communicate the quality and reliability of a health app. Consumers, patients, carers, health care professionals and their organizations, health authorities, health insurers and the wider public can use the health app quality label and report when recommending or selecting a health app for use, or for adoption in care guidelines, care pathways and care contracts.NOTE 1 Health apps can be subject to national legislation, such as for medical devices.NOTE 2 See Annex C for additional details on the scope.Outside the scope of this document are guidelines to comply to the medical device regulation.
This document provides quality requirements for health apps and defines a health app quality label in order to visualize the quality and reliability of health apps.
This document is applicable to health apps, which are a special form of health software. It covers the entire life cycle of health apps.
This document is intended for use by app manufacturers as well as app assessment organizations in order to communicate the quality and reliability of a health app. Consumers, patients, carers, health care professionals and their organizations, health authorities, health insurers and the wider public can use the health app quality label and report when recommending or selecting a health app for use, or for adoption in care guidelines, care pathways and care contracts.
NOTE 1 Health apps can be subject to national legislation, such as for medical devices.
NOTE 2 See Annex C for additional details on the scope.
Outside the scope of this document are guidelines to comply to the medical device regulation.
Le service Exigences vous aide à repérer rapidement au sein du texte normatif :
- les clauses impératives à satisfaire,
- les clauses non indispensables mais utiles à connaitre, telles que les permissions et les recommandations.
L’identification de ces types de clauses repose sur le document « Directives ISO/IEC, Partie 2 - Principes et règles de structure et de rédaction des documents ISO » ainsi que sur une liste de formes verbales constamment enrichie.
Avec Exigences, accédez rapidement à l’essentiel du texte normatif !

COBAZ est la solution simple et efficace pour répondre aux besoins normatifs liés à votre activité, en France comme à l’étranger.
Disponible sur abonnement, CObaz est LA solution modulaire à composer selon vos besoins d’aujourd’hui et de demain. Découvrez vite CObaz !
Demandez votre démo live gratuite, sans engagement
Je découvre COBAZ