NA 176

DIN Standards Committee Health Technologies

DIN EN ISO 21090 [CURRENT] referenced in following documents:

Document number Edition Title
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 CEN ISO/TS 20451 ; DIN SPEC 13264:2018-11 2018-11 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 (ISO/TS 20451:2017); English version CEN ISO/TS 20451:2018 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 21549-2 2014-06 Health informatics - Patient healthcard data - Part 2: Common objects (ISO 21549-2:2014); English version EN ISO 21549-2:2014 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