DIN CEN ISO/TS 16791 references following documents:
| Document number | Edition | Title |
|---|---|---|
| ISO 11615 | 2017-10 | Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information More |
| ISO/TS 19256 | 2016-06 | Health informatics - Requirements for medicinal product dictionary systems for health care More |
| DIN CEN ISO/TS 19256 ; DIN SPEC 13236:2017-06 | 2017-06 | Health informatics - Requirements for medicinal product dictionary systems for health care (ISO/TS 19256:2016); English version CEN ISO/TS 19256:2017 More |
| DIN CEN ISO/TS 19293 ; DIN SPEC 13239:2018-08 | 2018-08 | Health Informatics - Requirements for a record of the dispense of a medicinal product (ISO/TS 19293:2018); English version CEN ISO/TS 19293:2018 More |
| DIN CEN ISO/TS 20443 ; DIN SPEC 13263:2018-11 | 2018-11 | Health informatics - Identification of medicinal products - Implementation guidelines for ISO 11615 data elements and structures for the unique identification and exchange of regulated medicinal product information (ISO/TS 20443:2017); English version CEN ISO/TS 20443:2018 More |
| DIN EN ISO 11238 | 2018-11 | 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 More |
| DIN EN ISO 11240 | 2013-03 | 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 More |
| DIN EN ISO 11616 | 2018-04 | Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information (ISO 11616:2017); German version EN ISO 11616:2017 More |
| DIN EN ISO 27953-1 | 2012-09 | 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 More |
| DIN EN ISO 27953-2 | 2012-09 | 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 More |
