NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 11616 [CURRENT] 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 11240 | 2012-11 | Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of units of measurement More |
| ISO/TS 20443 | 2017-10 | 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 More |
| ISO/TS 20451 | 2017-10 | Health informatics - Identification of medicinal products - Implementation guidelines for ISO 11616 data elements and structures for the unique identification and exchange of regulated pharmaceutical product information More |
| DIN CEN ISO/TS 19844 ; DIN SPEC 13261:2017-12 | 2017-12 | Health informatics - Identification of medicinal products - Implementation guidelines for data elements and structures for the unique identification and exchange of regulated information on substances (ISO/TS 19844:2016); English version CEN ISO/TS 19844:2017, only on CD-ROM 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 21090 | 2011-06 | Health Informatics - Harmonized data types for information interchange (ISO 21090:2011); English version EN ISO 21090:2011, only on CD-ROM 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 |
| EGV 1394/2007 | 2007-11-13 | Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004 More |
