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ISO 1087-1:2000
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Terminology work Vocabulary Part 1: Theory and application |
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DIN EN ISO 11616:2016-09 (Draft)
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HEALTH INFORMATICS - IDENTIFICATION OF MEDICINAL PRODUCTS - DATA ELEMENTS AND STRUCTURES FOR THE UNIQUE IDENTIFICATION AND EXCHANGE OF REGULATED PHARMACEUTICAL PRODUCT INFORMATION (ISO 11616:2017) |
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DIN EN ISO 11615:2016-09 (Draft)
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HEALTH INFORMATICS - IDENTIFICATION OF MEDICINAL PRODUCTS - DATA ELEMENTS AND STRUCTURES FOR THE UNIQUE IDENTIFICATION AND EXCHANGE OF REGULATED MEDICINAL PRODUCT INFORMATION (ISO 11615:2017) |
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EN 1614 : 2006
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HEALTH INFORMATICS - REPRESENTATION OF DEDICATED KINDS OF PROPERTY IN LABORATORY MEDICINE |
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ISO 11615:2017
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Health informatics — Identification of medicinal products — Data elements and structures for the unique identification and exchange of regulated medicinal product information |
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ISO/IEC 9834-1:2012
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Information technology — Procedures for the operation of object identifier registration authorities — Part 1: General procedures and top arcs of the international object identifier tree |
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ISO/HL7 27953-2:2011
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Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 2: Human pharmaceutical reporting requirements for ICSR |
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ISO/HL7 27951:2009
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Health informatics Common terminology services, release 1 |
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ISO 21090:2011
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Health informatics — Harmonized data types for information interchange |
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ISO/IEC Guide 99:2007
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International vocabulary of metrology Basic and general concepts and associated terms (VIM) |
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ENV 13607:2000
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HEALTH INFORMATICS - MESSAGES FOR THE EXCHANGE OF INFORMATION ON MEDICINE PRESCRIPTIONS |
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ISO 11238:2012
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Health informatics Identification of medicinal products Data elements and structures for the unique identification and exchange of regulated information on substances |
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ISO 11616:2017
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Health informatics — Identification of medicinal products — Data elements and structures for unique identification and exchange of regulated pharmaceutical product information |
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ENV 12610 : DRAFT 1997
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MEDICAL INFORMATICS - MEDICINAL PRODUCT IDENTIFICATION |
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DIN EN ISO 27953-1:2012-09
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HEALTH INFORMATICS - INDIVIDUAL CASE SAFETY REPORTS (ICSRS) IN PHARMACOVIGILANCE - PART 1: FRAMEWORK FOR ADVERSE EVENT REPORTING (ISO 27953-1:2011) |
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DIN EN ISO 9000:2015-11
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QUALITY MANAGEMENT SYSTEMS - FUNDAMENTALS AND VOCABULARY (ISO 9000:2015) |
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ISO 9000:2015
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Quality management systems — Fundamentals and vocabulary |
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ISO/HL7 27953-1:2011
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Health informatics — Individual case safety reports (ICSRs) in pharmacovigilance — Part 1: Framework for adverse event reporting |
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DIN EN ISO 11239:2013-03
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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 11239:2012) |
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DIN EN ISO 11238:2013-03
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HEALTH INFORMATICS - IDENTIFICATION OF MEDICINAL PRODUCTS - DATA ELEMENTS AND STRUCTURES FOR THE UNIQUE IDENTIFICATION AND EXCHANGE OF REGULATED INFORMATION ON SUBSTANCES (ISO 11238:2012) |
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EN 14463:2007
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Health informatics - A syntax to represent the content of medical classification systems - ClaML |
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DIN EN ISO 27953-2:2012-09
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HEALTH INFORMATICS - INDIVIDUAL CASE SAFETY REPORTS (ICSRS) IN PHARMACOVIGILANCE - PART 2: HUMAN PHARMACEUTICAL REPORTING REQUIREMENTS FOR ICSR (ISO 27953-2:2011) |
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EN 12435 : 2006
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HEALTH INFORMATICS - EXPRESSION OF RESULTS OF MEASUREMENTS IN HEALTH SCIENCES |
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DIN EN ISO 21090:2011-06
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HEALTH INFORMATICS - HARMONIZED DATA TYPES FOR INFORMATION INTERCHANGE |
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ISO 11239:2012
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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 |