About CEN
The European Committee for Standardization is one of three European Standardization Organizations (together with CENELEC and ETSI) that have been officially recognized by the European Union and by the European Free Trade Association (EFTA) as being responsible for developing and defining voluntary standards at European level.
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Project
| Reference | EN ISO 21860:2024 |
|---|---|
| Title | Health Informatics - Reference standards portfolio (RSP) - Clinical imaging (ISO 21860:2020) |
| Work Item Number | 00251398 |
| Abstract/Scope | This document establishes the Reference Standards Portfolio (RSP) for the clinical imaging domain (as defined in Clause 4). An RSP lists the principle health information technology (HIT) standards that form the basis of implementing and deploying interoperable applications in the target domain. An RSP includes a description of the domain, a normative list of standards, and an informative framework for mapping the standards to example deployment use cases. The lists do not include standards that are specifically national in scope. The primary target audience for this document is policy makers (governmental or organizational), regulators, project planners and HIT managers. This document will also be of interest to other stakeholders such as equipment and HIT vendors, clinical and health information management (HIM) professionals and standards developers. The intended usage of this document is to inform decisions about selecting the standards that will form the basis of integration projects in geographic regions or healthcare organizations. For example: — What standards to use for capturing/encoding/exchanging certain types of information — What standards to use for interfaces between the devices and information systems that support information capture, management, exchange, processing and use — What standards to use for specific use cases/deployment scenarios The selected standards, and/or corresponding RSP clauses, might be useful when drafting project specifications. |
| Status |
Published
|
| Reference Document |
ISO 21860:2020 (EQV)
|
| date of Availability (DAV) | 2024-02-21 |
| ICS | 35.240.80 - IT applications in health care technology |
| A-Deviation(s) | |
| Special National Condition(s) |
Legal
| Directive(s) | |
|---|---|
| Mandate(s) | |
| Citation in OJEU |
Implementation Dates
| date of Ratification (DOR) (1) | 2024-02-12 |
|---|---|
| date of Availability (DAV) (2) | 2024-02-21 |
| date of Announcement (DOA) (3) | 2024-05-31 |
| date of Publication (DOP) (4) | 2024-08-31 |
| date of Withdrawal (DOW) (5) | 2024-08-31 |
Relations
| Supersedes | |
|---|---|
| Superseded by | |
| Normative reference (6) |
ANSI/HL7 CDA, R 2
ANSI/HL7 V 2.3.1 ANSI/HL7 V 2.5.1 |
| Sales Points |
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(1) Date of ratification (dor) date when the Technical Board notes the approval of an EN (and HD for CENELEC), from which time the standard may be said to be approved
(2) Date of availability (dav) date when the definitive text in the official language versions of an approved CEN/CENELEC publication is distributed by the Central Secretariat
(3) Date of announcement (doa) latest date by which the existence of an EN (and HD for CENELEC), a TS or a CWA has to be announced at national level
(4) Date of publication (dop) latest date by which an EN has to be implemented at national level by publication of an identical national standard or by endorsement
(5) Date of withdrawal (dow) latest date by which national standards conflicting with an EN (and HD for CENELEC) have to be withdrawn
(6) This list of normative references is purely indicative. The only official list of normative reference is the list of the published standard.
In the case of undated standard, a link to the last dated version is provided.
In the case of series, a link to each standard identified in the series is provided.
We also invite you to check (via the website) whether corrigenda and/or amendments shall be read in conjunction with the main standard.