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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...
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| 發表在: | Nat Rev Cardiol |
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| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2015
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| 主題: | |
| 在線閱讀: | 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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