BS EN ISO 17523:2016规定了适用于电子处方的要求。信息技术 描述对所有电子处方都很重要的通用原则。本国际标准的范围仅限于电子处方的内容 它本身是由开处方的医疗保健专业人员发布并由医生接收的数字文档 配药保健专业人员。处方药品应通过 一个被授权的医疗专业人员，目的是给人类患者服用药物。另外 信息、角色和场景（如处方验证、给药、药物图表、EHR） 对于患者，护理和配药产品的报销不在本国际协议的范围内 标准，因为他们或多或少是特定国家或地区的，由于文化和文化的差异 在医疗立法中。但是，电子处方的要求和内容 司法管辖区的背景与这些情景有关系。电子产品 提供或交换的处方也不属于本国际标准的范围。本国际标准适用于医药产品的电子处方。虽然 其他种类的产品（如医疗器械、伤口护理产品）可以通过 电子处方，本国际标准中的要求针对药品 具有市场授权的产品和配制的药物制剂 在药房里。电子处方是授权医疗服务的信息对象 专业人士合法分发药品。本国际标准规定了一系列数据元素，这些数据元素可被视为 电子处方，取决于辖区或临床环境（初级保健、医院等）。 ).交叉引用:ISO 8601ISO 11238ISO 11239ISO 11240ISO 11615ISO 11616ISO 17090-1ISO/TS 16791ISO/TS 2220ISO/TS 27527ISO 639-2ISO 639-2ISO 639-3ISO 7498-2:1989ISO 21549-7ISO/IEC 2382:2015ISO/IEC 24760-1:20112011/24/EU2012/52/EU2001/83/EU购买本文件时提供的所有现行修订版均包含在购买本文件中。

BS EN ISO 17523:2016 specifies the requirements that apply to electronic prescriptions. It describes generic principles that are considered important for all electronic prescriptions.The scope of this International Standard is constrained to the content of the electronic prescription itself, the digital document which is issued by a prescribing healthcare professional and received by a dispensing healthcare professional. The prescribed medicinal product is to be dispensed through an authorized healthcare professional with the aim of being administered to a human patient. Other messages, roles and scenarios (e.g. validation of a prescription, administration, medication charts, EHR of the patient, reimbursement of care and dispensed products) are out of scope of this International Standard, because they are more or less country or region specific, due to differences in culture and in legislation of healthcare. However, requirements and content of electronic prescriptions within the context of jurisdictions have a relationship with these scenarios. The way in which electronic prescriptions are made available or exchanged also fall outside the scope of this International Standard.This International Standard is applicable to electronic prescriptions of medicinal products. Although other kinds of products (e.g. medical devices, wound care products) can be ordered by means of an electronic prescription, the requirements in this International Standard are aimed at medicinal products that have a market authorization and at pharmaceutical preparations which are compounded in a pharmacy. An electronic prescription is an information object that authorizes a healthcare professional to legally dispense a medicinal product.This International Standard specifies a list of data elements that can be considered as essential for electronic prescriptions, depending on jurisdiction or clinical setting (primary healthcare, hospital, etc.).Cross References:ISO 8601ISO 11238ISO 11239ISO 11240ISO 11615ISO 11616ISO 17090-1ISO/TS 16791ISO/TS 22220ISO/TS 27527ISO 639-2ISO 639-3ISO 7498-2:1989ISO 21549-7ISO/IEC 2382:2015ISO/IEC 24760-1:20112011/24/EU2012/52/EU2001/83/EUAll current amendments available at time of purchase are included with the purchase of this document.