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Trust and transparency in clinical trials of medical devices

Regulatory approval of high-risk cardiovascular devices is on the basis of clinical studies submitted with a premarket approval application. Failure to publish many of these studies in peer-reviewed literature, and major discrepancies between premarket approval submissions and those studies that are...

詳細記述

保存先:
書誌詳細
出版年:Nat Rev Cardiol
主要な著者: Kramer, Daniel B., Cutlip, Donald E.
フォーマット: Artigo
言語:Inglês
出版事項: 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4698975/
https://ncbi.nlm.nih.gov/pubmed/26194550
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nrcardio.2015.112
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