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Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information - Amendment 1
Edition 2022-09-21

Standards [CURRENT]

BS EN ISO 11615+A1

Health informatics. Identification of medicinal products. Data elements and structures for the unique identification and exchange of regulated medicinal product information
Edition 2018-01-09

Standards [CURRENT]

PD CEN ISO/TS 20443

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
Edition 2018-05-24

Verordnung über die Mindestanforderungen an die Informationen in elektronischen Programmen für die Verordnung von Arzneimitteln durch Vertragsärzte und über die Veröffentlichung der Beschlüsse des Gemeinsamen Bundesausschusses (Elektronische Arzneimittelinformationen-Verordnung - EAMIV)
Edition 2019-08-01

Erste Verordnung zur Änderung der Elektronische Arzneimittelinformationen-Verordnung
Edition 2023-04-19

Technical rule [CURRENT]

DIN-Fachbericht CEN/TR 15753

Packaging - Package leaflets for medicinal products - Braille and other formats for visually impaired people; German version CEN/TR 15753:2008
Edition 2008-08

Standards [CURRENT]

DIN EN ISO 11616

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
Edition 2018-04

Standards [CURRENT]

DIN EN ISO 17523

Health informatics - Requirements for electronic prescriptions (ISO 17523:2016); German version EN ISO 17523:2016
Edition 2016-12

Standards [CURRENT]

DIN EN ISO 21976

Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018); German version EN ISO 21976:2020
Edition 2020-12

Standards [CURRENT]

DIN EN ISO 11239

Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (ISO 11239:2023); German version EN ISO 11239:2023
Edition 2023-10

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