STN P CEN ISO/TS 21405
| Name: | STN P CEN ISO/TS 21405 |
| Validity: | Valid |
| Number of pages: | 44 |
| Language: |
EN
|
| Paper: | 18,90€ |
| Electronic version |
a) Only read (without ability to print and copy)
17,01€ b) Without ability to print, with ability to copy (printscreen) 18,90€ c) With ability to print and copy (printscreen) 24,57€ |
| Slovak title | Zdravotnícka informatika. Identifikácia liekov. Metodika a rámec na vývoj a vyjadrenie ontológie IDMP (ISO/TS 21405: 2026) |
| English title | Health informatics - Identification of medicinal products - Methodology and framework for the development and representation of IDMP ontology (ISO/TS 21405:2026) |
| Release Date: | 01. 08. 2026 |
| Date of withdrawal: | |
| ICS: | 35.240.80 |
| Sorting character/National clasification code | 84 8139 |
| Level of incorporation: | idt CEN ISO/TS 21405:2026, idt ISO/TS 21405:2026 |
| Official Journal | 07/26 |
| Amendments | |
| Replaced by: | |
| Repleces: | |
| Note in Official Journal: | Táto predbežná slovenská technická norma je určená na overenie. Prípadné pripomienky pošlite do apríla 2028 Úradu pre normalizáciu, metrológiu a skúšobníctvo Slovenskej republiky. |
| Subject of the standard: | This document describes a standardized methodology and framework for the development and representation of an ontology that supports a global, open-source approach to implementing the ISO standards on the identification of medicinal products (IDMP) (ISO 11615, ISO/TS 20443, ISO/TS 20451, ISO 11238; ISO/TS 19844, ISO 11239, ISO/TS 20440, and ISO 11240). Realization of the full potential of IDMP requires fully self-describing data. For this purpose, this document describes a methodology and framework that complements the existing conceptual and logical models in the ISO documents on IDMP with an IDMP ontology that enables deep, semantic interoperability based on findable, accessible, interoperable and reusable (FAIR) data principles. This methodology and framework enhance the usage of the IDMP data model as the foundation of medicinal product identification and will ultimately enable collaboration towards drug safety and overall operational efficiency. This document also describes a methodology for the ... |
| Preview: | Náhľad normy (PDF) |