Active standard | Published: 19/10/2017

ISO/TS 20443:2017

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
(Informatique de santé — Identification des médicaments — Lignes directrices pour l’implémentation des éléments de données et structures ISO 11615 pour l’identification unique et l’échange d’informations réglementées sur les médicaments)

Available languages: English

Available design: electronic design (pdf), Print design

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Detail information

Designation: ISO/TS 20443:2017

Publication date: 19/10/2017

Pages: 202

Country: International technical standard

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Anotation

Description / Abstract: ISO/TS 20443:2017 defines concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products. Taken together, all ISO IDMP standards (ISO 11615, ISO 11616, ISO 11238, ISO 11239 and ISO 11240) define, characterise, and uniquely identify regulated Medicinal Products for human use from approval, to post-marketing and renewal or withdrawal from the market, where applicable. Furthermore, to support successful information exchange in relation to the unique identification and characterisation of Medicinal Products, the normative use of HL7 common product model (CPM) and structured product labeling (SPL) messaging is described. References to the use of other relevant standards for Medicinal Product information are included in ISO/TS 20443:2017 to support successful information exchange.

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