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The Swedish Medical Products Agency's rules of procedure.

作者信息

Andersson Forsman Catarina

机构信息

Swedish Medical Products Agency, SE -751 03, Uppsala, Sweden.

出版信息

Health Res Policy Syst. 2018 Nov 15;16(1):100. doi: 10.1186/s12961-018-0372-3.

DOI:10.1186/s12961-018-0372-3
PMID:30428898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6237002/
Abstract
摘要

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引用本文的文献

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Decisions in health technology assessment: should we speak with one voice?卫生技术评估决策:我们是否应该同声同气?
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Regulatory scientists' work has important ramifications for public health and should be open to public scrutiny.监管科学家的工作对公共健康有重要影响,应该接受公众的审查。
Health Res Policy Syst. 2018 Nov 15;16(1):98. doi: 10.1186/s12961-018-0371-4.

本文引用的文献

1
Why European and United States drug regulators are not speaking with one voice on anti-influenza drugs: regulatory review methodologies and the importance of 'deep' product reviews.为什么欧洲和美国的药品监管机构在抗流感药物问题上不能发出一致的声音:监管审查方法和“深入”产品审查的重要性。
Health Res Policy Syst. 2017 Nov 9;15(1):93. doi: 10.1186/s12961-017-0259-8.