ГОСТР ИСО 11239—2014
Библиография
[1] ISO 11238, Health informatics — Identification of medicinal products — Data elements and
structures for the unique identification and exchange of regulated information on substances
[2] ISO 11240, Health informatics — Identification of medicinal products — Data elements and
structures for the unique identification and exchange of units of measurement
[3] ISO 11615, Health informatics — Identification of medicinal products — Data elements and
structures for the unique identification and exchange of regulated medicinal product information
[4J ISO 11616, Health informatics — Identification of medicinal products — Data elements and
structures for the unique identification and exchange of regulated pharmaceutical product information
[5] ENV 12610:1997, Medical informatics — Medicinal product information
[6] ENV 13607:2000, Health informatics — Messages for the exchange of information on medicine
prescriptions
[7] HL7 Version 2 Standard, Common Terminology Services (CTS) HL7 Draft Standard for Trial Use
DSTU Release 2.14 October 2009, HL7 Inc.
[8] HL7 Core Principles and Properties of HL7 Version 3 Models
[9] International Conference on Harmonisation of Technical Requirements for Registration of
Pharmaceuticals for Human Use Draft Consensus Guideline — Data Elements and Standards for Drug
Dictionaries — M5 Revision 4. 2 February 2007
[10]European Directive 65/65/EEC, Approximation of provisions laid down by law, regulation or
administrative action relating to medicinal products, January 26,1965
[11]European Directive 92/27/EEC, Labelling of medicinal products for human use and on package
leaflets. March 31,1992
[12] CDISC Controlled Terminology, National Cancer Institute Enterprise Vocabulary Services
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