Why Industry-Wide Standards Matter In Fulfilling the Intent of DSCSA

Christiane Wirrig, PhD, David Kessler
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引用次数: 0

Abstract

Speakers discuss the importance of standardization in order to digitalize the U.S. pharmaceutical supply chain as motivated by the Drug Supply Chain Security Act (DSCSA). Key topics What is DSCSA? What does FDA’s Stabilization Period mean? Why do technology standards matter and how are they being implemented, i.e. interoperability through standards? Focus on standardization, due diligence in the context of DSCSA-regulated digitally managed pharma supply chain 2023 readiness in relation to stabilization period until 2024 Inspections will keep happening ATP is mandatory, authentication & authorization Data security
为什么全行业标准对实现 DSCSA 的意图至关重要?
演讲者讨论了标准化的重要性,以便在药品供应链安全法案(DSCSA)的推动下实现美国药品供应链的数字化。什么是DSCSA?FDA的稳定期意味着什么?为什么技术标准很重要,它们是如何实现的,即通过标准实现互操作性?在dscsa监管的数字化管理制药供应链2023年准备就绪的背景下,专注于标准化,尽职调查,直至2024年的稳定期,检查将继续进行ATP是强制性的,认证和授权数据安全
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来源期刊
CiteScore
2.40
自引率
0.00%
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0
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