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现行 ISO/TR 18728:2025
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Health informatics — Global medicinal product and ingredient and batch registration as part of identification of medicinal products (IDMP) 健康信息学-作为药品鉴定(IDMP)一部分的全球药品和成分及批次注册
发布日期: 2025-12-12
本文档展示了通过利用药品验证或认证系统(或两者兼而有之)、可追溯性工具、安全通信技术解决方案等来监控医疗保健供应链中实施的供应链的现有实践。 本文件还讨论了扩展药品识别(IDMP)以提供药品、成分和批次的全球标识符的潜在好处。它还讨论了全球注册系统的潜在途径。

This document showcases existing practices to monitor supply chains as implemented in the healthcare supply chains, by making use of medicines verification or authentication systems, or both, traceability tools, safe communication technology solutions, and more.

This document also discusses the potential benefits of expanding the identification of medicinal products (IDMP) to provide global identifiers for medicinal products, ingredients and batches. It also addresses potential pathways to a global registration system.

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归口单位: ISO/TC 215
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