This International Standard specifies:<\/p>\n
the data elements, structures and relationships between the data elements required for the exchange of information, which uniquely and with certainty identify pharmaceutical dose forms, units of presentation, routes of administration and packaging items (containers, closures and administration devices) related to medicinal products;<\/p>\n<\/li>\n
a mechanism for the association of translations of a single concept into different languages, which is an integral part of the information exchange;<\/p>\n<\/li>\n
a mechanism for the versioning of the concepts in order to track their evolution;<\/p>\n<\/li>\n
rules to allow regional authorities to map existing regional terms to the terms created using this International Standard, in a harmonized and meaningful way.<\/p>\n<\/li>\n<\/ul>\n
In addition, to support the successful application of this International Standard, references to standards concerned with identification of medicinal products (IDMP) and messaging for medicinal product information are provided as required.<\/p>\n
| PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
|---|---|---|---|---|---|---|---|
| 6<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
| 7<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
| 9<\/td>\n | 1\tScope 2\tNormative references 3\tTerms, definitions and abbreviations 3.1\tTerms and definitions <\/td>\n<\/tr>\n | ||||||
| 13<\/td>\n | 3.2\tAbbreviations <\/td>\n<\/tr>\n | ||||||
| 14<\/td>\n | 4\tRequirements 4.1\tGeneral requirements for controlled vocabularies <\/td>\n<\/tr>\n | ||||||
| 15<\/td>\n | 4.2\tRequirements for use within the IDMP set of standards 5\tSchema 5.1\tGeneral <\/td>\n<\/tr>\n | ||||||
| 16<\/td>\n | 5.2\tConceptual models\u00a0\u2014 Supporting concepts <\/td>\n<\/tr>\n | ||||||
| 18<\/td>\n | 5.3\tConceptual models\u00a0\u2014 High-level concepts <\/td>\n<\/tr>\n | ||||||
| 25<\/td>\n | Annex\u00a0A \n(informative)<\/p>\n Examples of controlled vocabularies <\/td>\n<\/tr>\n | ||||||
| 31<\/td>\n | Annex\u00a0B \n(informative)<\/p>\n Examples of controlled vocabularies to describe medicinal products <\/td>\n<\/tr>\n | ||||||
| 36<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" 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<\/b><\/p>\n |