Lanean...
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...
Gorde:
| Argitaratua izan da: | Nat Rev Cardiol |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2015
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| Gaiak: | |
| Sarrera elektronikoa: | 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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