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oSIST prEN ISO/IEEE 11073-10472:2024

(Main)

Health informatics - Device interoperability - Part 10472: Personal Health Device Communication - Device Specialization - Medication Monitor (ISO/IEEE FDIS 11073-10472:2024)

Health informatics - Device interoperability - Part 10472: Personal Health Device Communication - Device Specialization - Medication Monitor (ISO/IEEE FDIS 11073-10472:2024)

Within the context of the ISO/IEEE 11073 family of standards for device communication, ISO/IEEE 11073-10472:2012 establishes a normative definition of communication between personal telehealth medication monitor devices and compute engines (e.g. cell phones, personal computers, personal health appliances, set top boxes) in a manner that enables plug-and-play interoperability. It leverages appropriate portions of existing standards including ISO/IEEE 11073 terminology, information models, application profile standards, and transport standards. It specifies the use of specific term codes, formats, and behaviors in telehealth environments restricting optionality in base frameworks in favor of interoperability. ISO/IEEE 11073-10472:2012 defines a common core of communication functionality for personal telehealth medication monitor devices.

Medizinische Informatik - Interoperabilität von Geräten - Teil 10472: Kommunikation von Geräten für die persönliche Gesundheit - Gerätespezialisierung - Medikamentenmonitoring (ISO/IEEE FDIS 11073-10472:2024)

Informatique de santé - Interopérabilité des dispositifs - Partie 10472: Titre manque (ISO/IEEE FDIS 11073-10472:2024)

Dans le contexte de la famille de normes ISO/IEEE 11073 relatives à la communication de dispositifs, l'ISO/IEEE 11073-10472:2012 établit une définition normative de la communication entre des dispositifs de surveillance de médication et des gestionnaires (par exemple, des téléphones cellulaires, des ordinateurs personnels, des équipements personnels de santé et des boîtiers décodeurs) d'une manière qui permet une interopérabilité du type prêt à l'emploi. Elle s'appuie sur les parties appropriées de normes existantes, y compris la terminologie et les modèles d'informations de l'ISO/IEEE 11073. Elle spécifie l'utilisation de codes, de formats et de comportements en termes spécifiques dans les environnements de télésanté, en limitant les choix à des cadres de travail de base en faveur de l'interopérabilité. L'ISO/IEEE 11073-10472:2012 définit un noyau commun de fonctionnalités de communication pour les moniteurs de surveillance de médication.

Zdravstvena informatika - Interoperabilnost naprav - 10472. del: Komunikacija osebnih medicinskih naprav - Specialne naprave - Naprava za nadzor jemanja zdravil (ISO/IEEE FDIS 11073-10472:2024)

General Information

Status
Not Published
Public Enquiry End Date
29-Jun-2024
ICS
35.240.80 - IT applications in health care technology
Technical Committee
ITC - Information technology
Current Stage
4020 - Public enquire (PE) (Adopted Project)
Start Date
22-Apr-2024
Due Date
09-Sep-2024
Ref Project
prEN ISO/IEEE 11073-10472 - Health informatics - Device interoperability - Part 10472: Personal Health Device Communication - Device Specialization - Medication Monitor (ISO/IEEE FDIS 11073-10472:2024)

Relations

Revises
SIST EN ISO 11073-10472:2013 - Health Informatics - Personal health device communication - Part 10472: Device specialization - Medication monitor (ISO 11073-10472:2012)
Effective Date
08-Nov-2023

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SLOVENSKI STANDARD
oSIST prEN ISO/IEEE 11073-10472:2024
01-junij-2024
Zdravstvena informatika - Interoperabilnost naprav - 10472. del: Komunikacija
osebnih medicinskih naprav - Specialne naprave - Naprava za nadzor jemanja
zdravil (ISO/IEEE FDIS 11073-10472:2024)
Health informatics - Device interoperability - Part 10472: Personal Health Device
Communication - Device Specialization - Medication Monitor (ISO/IEEE FDIS 11073-
10472:2024)
Medizinische Informatik - Interoperabilität von Geräten - Teil 10472: Kommunikation von
Geräten für die persönliche Gesundheit - Gerätespezialisierung -
Medikamentenmonitoring (ISO/IEEE FDIS 11073-10472:2024)
Informatique de santé - Interopérabilité des dispositifs - Partie 10472: Titre manque
(ISO/IEEE FDIS 11073-10472:2024)
Ta slovenski standard je istoveten z: prEN ISO/IEEE 11073-10472
ICS:
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
oSIST prEN ISO/IEEE 11073-10472:2024 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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oSIST prEN ISO/IEEE 11073-10472:2024

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oSIST prEN ISO/IEEE 11073-10472:2024
FINAL DRAFT
International
Standard
ISO/IEEE
FDIS
11073-10472
ISO/TC 215
Health informatics — Device
Secretariat: ANSI
interoperability —
Voting begins on:
2024-04-11
Part 10472:
Personal Health Device
Voting terminates on:
2024-08-29
Communication — Device
Specialization — Medication
Monitor
This document is circulated as received from the committee secretariat.
FAST TRACK PROCEDURE
RECIPIENTS OF THIS DRAFT ARE INVITED TO SUBMIT,
WITH THEIR COMMENTS, NOTIFICATION OF ANY
RELEVANT PATENT RIGHTS OF WHICH THEY ARE AWARE
AND TO PROVIDE SUPPOR TING DOCUMENTATION.
IN ADDITION TO THEIR EVALUATION AS
BEING ACCEPTABLE FOR INDUSTRIAL, TECHNO­
ISO/CEN PARALLEL PROCESSING LOGICAL, COMMERCIAL AND USER PURPOSES, DRAFT
INTERNATIONAL STANDARDS MAY ON OCCASION HAVE
TO BE CONSIDERED IN THE LIGHT OF THEIR POTENTIAL
TO BECOME STAN DARDS TO WHICH REFERENCE MAY BE
MADE IN NATIONAL REGULATIONS.
Reference number
ISO/IEEE FDIS 11073­10472:2024(en) © IEEE 2024

---------------------- Page: 3 ----------------------
oSIST prEN ISO/IEEE 11073-10472:2024
FINAL DRAFT
ISO/IEEE FDIS 11073-10472:2024(en)
International
Standard
ISO/IEEE
FDIS
11073-10472
ISO/TC 215
Health informatics — Device
Secretariat: ANSI
interoperability —
Voting begins on:
Part 10472:
Personal Health Device
Voting terminates on:
Communication — Device
Specialization — Medication
Monitor
This document is circulated as received from the committee secretariat.
FAST TRACK PROCEDURE
RECIPIENTS OF THIS DRAFT ARE INVITED TO SUBMIT,
WITH THEIR COMMENTS, NOTIFICATION OF ANY
RELEVANT PATENT RIGHTS OF WHICH THEY ARE AWARE
COPYRIGHT PROTECTED DOCUMENT
AND TO PROVIDE SUPPOR TING DOCUMENTATION.
IN ADDITION TO THEIR EVALUATION AS
© IEEE 2024
BEING ACCEPTABLE FOR INDUSTRIAL, TECHNO­
ISO/CEN PARALLEL PROCESSING
LOGICAL, COMMERCIAL AND USER PURPOSES, DRAFT
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
INTERNATIONAL STANDARDS MAY ON OCCASION HAVE
be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting on
TO BE CONSIDERED IN THE LIGHT OF THEIR POTENTIAL
the internet or an intranet, without prior written permission. Permission can be requested from IEEE at the address below.
TO BECOME STAN DARDS TO WHICH REFERENCE MAY BE
MADE IN NATIONAL REGULATIONS.
Institute of Electrical and Electronics Engineers, Inc
3 Park Avenue, New York
NY 10016-5997, USA
Email: stds.ipr@ieee.org
Website: www.ieee.org
Published in Switzerland Reference number
ISO/IEEE FDIS 11073­10472:2024(en) © IEEE 2024

© IEEE 2024 – All rights reserved
ii

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oSIST prEN ISO/IEEE 11073-10472:2024
ISO/IEEE 11073-10472:2024(en)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards
bodies (ISO member bodies). The work of preparing International Standards is normally carried out through
ISO technical committees. Each member body interested in a subject for which a technical committee has
been established has the right to be represented on that committee. International organizations,
governmental and non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely
with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
The procedures used to develop this document and those intended for its further maintenance are described
in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the different types of
ISO document should be noted (see
...

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