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Technical Specification

DIN CEN ISO/TS 22703

Health informatics - Requirements for medication safety alerts (ISO/TS 22703:2021); German version CEN ISO/TS 22703:2021
Edition 2022-02

Standards [CURRENT]

DIN EN ISO 11238

Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on substances (ISO 11238:2018); German version EN ISO 11238:2018
Edition 2018-11

Standards [CURRENT]

DIN EN ISO 11240

Health informatics - Identification of medicinal products - Data elements and structures for unique identification and exchange of units of measurement (ISO 11240:2012); German version EN ISO 11240:2012
Edition 2013-03

Standards [CURRENT]

DIN EN ISO 27953-2

Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 2: Human pharmaceutical reporting requirements for ICSR (ISO 27953-2:2011); German and English version EN ISO 27953-2:2011, only on CD-ROM
Edition 2012-09

Standards [CURRENT]

DIN EN ISO 27269

Health informatics - International patient summary (ISO 27269:2021); German version EN ISO 27269:2022
Edition 2022-08

Draft standard [New]

DIN EN ISO 17523

Health informatics - Requirements for electronic prescriptions (ISO/DIS 17523:2024); English version prEN ISO 17523:2024
Edition 2024-08

Standards [CURRENT]

DIN EN ISO 13606-3

Health informatics - Electronic health record communication - Part 3: Reference archetypes and term lists (ISO 13606-3:2019); English version EN ISO 13606-3:2019
Edition 2019-11

Draft standard [New]

DIN EN ISO 13940

Health informatics - System of concepts to support continuity of care (ISO/DIS 13940:2024); English version prEN ISO 13940:2024
Edition 2024-08

Standards [CURRENT]

DIN EN ISO 27953-1

Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 1: Framework for adverse event reporting (ISO 27953-1:2011); German and English version EN ISO 27953-1:2011, only on CD-ROM
Edition 2012-09

Standards [CURRENT]

DIN EN ISO 12417-1

Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015); German version EN ISO 12417-1:2015
Edition 2016-02

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