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Evaluation of Compliance With Legal Requirements Under the FDA Amendments Act of 2007 for Timely Registration of Clinical Trials, Data Verification, Delayed Reporting, and Trial Document Submission
This cross-sectional study evaluates clinical trials’ rates of compliance with the legal requirements of the US Food and Drug Administration’s Amendments Act of 2007 for timely registration of clinical trials, data verification, delayed reporting, and trial document submission.
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| Publicado no: | JAMA Intern Med |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Medical Association
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8145152/ https://ncbi.nlm.nih.gov/pubmed/34028509 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamainternmed.2021.2036 |
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