by Ursula Tschorn | Jul 5, 2015
The EMA and the EU Regulatory Network have founded an EU IDMP Task Force with the involvement of terminology organisations, software vendors and developers of medicinal products dictionaries or databases. The task force will be responsible for advising on the...
by Ursula Tschorn | May 24, 2015
ISO 11616 International Standard “Health informatics — Identification of Medicinal Products — Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information”. ISO 11616 is intended to assist...
by Ursula Tschorn | May 22, 2015
ISO 11240 – Units of Measurement What ISO 11240 does: specifies rules for the usage of units of measurement for IDMP specifies requirements for traceability to metrological standards establish reference code system for units provide structures and rules for...
by Ursula Tschorn | May 22, 2015
ISO 11615 establishes definitions and concepts required for the detailed description and unique identification of medicinal products. The scope of ISO 11615 ISO 11615 describes data elements and regulated medicinal product information during their entire life cycle...
by Ursula Tschorn | May 22, 2015
ISO 11239 IDMP Standard lists regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging. The ISO 11239 standard identifies for example injection solution, injection suspension, infusion solution (or a less...
