DS/ISO/TR 18728:2025
Current
Current
The latest, up-to-date edition.
Health informatics – Global medicinal product and ingredient and batch registration as part of identification of medicinal products (IDMP)
Published date
17-12-2025
Publisher
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This document showcases existing practices to monitor supply chains as implemented in the healthcare supply chains, by making use of medicines verification or authentication systems, or both, traceability tools, safe communication technology solutions, and more.
| Committee |
DS/S-273
|
| DocumentType |
Technical Report
|
| ProductNote |
This standard is also refer to " ISO 22532"
|
| PublisherName |
Danish Standards
|
| Status |
Current
|
| Standards | Relationship |
| ISO/TR 18728:2025 | Identical |
| ISO/IEC 15459-4:2014 | Information technology — Automatic identification and data capture techniques — Unique identification — Part 4: Individual products and product packages |
| 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 |
| ISO/IEC 19988:2024 | Information technology — GS1 Core Business Vocabulary (CBV) |
| ISO 11615:2017 | Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated medicinal product information |
| ISO 11239:2023 | 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 11240:2012 | Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of units of measurement |
| ISO 11616:2017 | Health informatics — Identification of medicinal products — Data elements and structures for unique identification and exchange of regulated pharmaceutical product information |
| ISO/TS 16791:2020 | Health informatics — Requirements for international machine-readable coding of medicinal product package identifiers |
| ISO 11238:2018 | Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated information on substances |
| ISO/TR 14872:2025 | Health informatics — Identification of medicinal products — Core principles for maintenance of identifiers and terms |
| ISO/TS 19844:2018 | Health informatics — Identification of medicinal products (IDMP) — Implementation guidelines for ISO 11238 for data elements and structures for the unique identification and exchange of regulated information on substances |
| ISO/IEC 19987:2024 | Information technology — EPC Information Services (EPCIS) |
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