C07 电子计算机应用 标准查询与下载
共找到 1093 条与 电子计算机应用 相关的标准，共 73 页
Health informatics. Identification of medicinal products Data elements and structures for the unique identification and exchange of regulated information on substances
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11-30
- 实施
- 2012-11-30
This International Standard establishes definitions and concepts and describes data elements and their structural relationships, which are required for the unique identification and the detailed description of Medicinal Products. Taken together, the standards listed in the introduction define, characterize and uniquely identify regulated Medicinal Products for human use during their entire life cycle, i.e. from development to authorization, postmarketing and renewal or withdrawal from the market, where applicable. Furthermore, to support successful information exchange in relation to the unique identification and characterization of Medicinal Products, the use of other normative IDMP messaging standards is included, which are to be applied in the context of this International Standard.
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated medicinal product information
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
This International Standard specifies: — 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; — a mechanism for the association of translations of a single concept into different languages, which is an integral part of the information exchange; — a mechanism for the versioning of the concepts in order to track their evolution; — rules to allow regional authorities to map existing regional terms to the terms created using this International Standard, in a harmonized and meaningful way. 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.
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
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
Health informatics - Personal health device communication - Part 10420: Device specialization - Body composition analyzer
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
Health informatics - Personal health device communication - Part 10421: Device specialization - Peak expiratory flow monitor (peak flow)
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
Health informatics - Clinical knowledge resources - Metadata
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
This International Standard is intended to provide specific levels of information relevant to the identification of a medicinal product or group of medicinal products. It defines the data elements, structures and relationships between data elements that are required for the exchange of regulated information, in order to uniquely identify pharmaceutical products. This identification is to be applied throughout the product lifecycle to support pharmacovigilance, regulatory and other activities worldwide. In addition, this International Standard is essential to ensuring that pharmaceutical product information is assembled in a structured format with transmission between a diverse set of stakeholders. This ensures interoperability and compatibility for both the sender and the recipient. This International Standard is not intended to be a scientific classification for pharmaceutical products. Rather, it is a formal association of particular data elements categorized in prescribed combinations and uniquely identified when levelling degrees of information are incomplete. This allows for medicinal products to be unequivocally identified. References to other normative IDMP and messaging standards for pharmaceutical product information are included in Clause 2, to be applied in the context of this International Standard. Medicinal products for veterinary use are out of scope of this International Standard.
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated pharmaceutical product information
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
Health informatics - Point-of-care medical device communication - Part 30400: Interface profile - Cabled Ethernet
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
Health Informatics - Personal health device communication - Part 10472: Device specialization - Medication monitor
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
This International Standard: — specifies rules for the usage and coded representation of units of measurement for the purpose of exchanging information about quantitative medicinal product characteristics that require units of measurement (e.g. strength) in the human medicine domain; — establishes requirements for units in order to provide traceability to international metrological standards; — provides rules for the standardized and machine-readable documentation of quantitative composition and strength of medicinal products, specifically in the context of medicinal product identification; — defines the requirements for the representation of units of measurement in coded form; — provides structures and rules for mapping between different unit vocabularies and language translations to support the implementation of this International Standard, taking into account that existing systems, dictionaries and repositories use a variety of terms and codes for the representation of units. The scope of this International Standard is limited to the representation of units of measurement for data interchange between computer applications.
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of units of measurement
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on substances
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-11
- 实施
Health informatics. Electronic health record communication. Reference model
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-10-31
- 实施
- 2012-10-31
Health informatics. Categorial structure for terminological systems of surgical procedures
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-09-30
- 实施
- 2012-09-30
Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 2: Human pharmaceutical reporting requirements for ICSR (ISO 27953-2:2011); German and English version EN ISO 27953-2:2011, only on CD-ROM
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-09
- 实施
This International Standard specifies the minimal characteristics of a categorial structure for terminological systems of surgical procedures and the minimal domain constraints to support interoperability, comparability and the exchange of meaningful information on surgical procedures, independently of the language, insofar as the significant differences are specified by the system. Further characteristics or more detailed value sets can be used for specific purposes. NOTE 2 Categorial structures support interoperability by providing common frameworks within which to develop terminological systems that can be related to each other, and to analyse the properties of different terminological systems in order to derive relationships between them. This International Standard is applicable to terminological systems of surgical procedures in all surgical disciplines. It covers only the terminology part, as defined in ISO 1087-1:2000, of the terminological systems of surgical procedures. It is intended to be used by: — organizations involved with the development or maintenance of terminological systems for surgical procedures, namely for multipurpose terminological systems on a national or international level; — organizations developing and maintaining software tools that allow natural clinical language expressions analysis, generation and mapping to the main existing terminological systems of surgical procedures. This International Standard is intended to be used as an integrated part of computer-based applications and for electronic health care records. It is of limited value for manual use. This International Standard is not suitable for, nor intended for use by, individual clinicians or hospital administrators. It is not the purpose of this International Standard to standardize the end user terminological system or to conflict with the concept systems embedded in national practice and languages.
Health informatics - Categorial structure for terminological systems of surgical procedures
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-09
- 实施
Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 1: Framework for adverse event reporting (ISO 27953-1:2011); German and English version EN ISO 27953-1:2011, only on CD-ROM
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-09
- 实施
Health informatics - Capacity-based eHealth architecture roadmap - Part 1: Overview of national eHealth initiatives
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-08
- 实施
Knowledge management of health information standards
- ICS
- 35.240.80
- CCS
- C07
- 发布
- 2012-08
- 实施
Disease Control Basic Data Set_Part 12: Vaccination
- ICS
- 11.02
- CCS
- C07
- 发布
- 2012-07-19
- 实施
- 2012-12-01
