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Reaping the Bounty of Publicly Available Clinical Trial Consent Forms
Public access to clinical trial consent forms, beyond those individuals involved in reviewing, conducting, or participating in a trial, has been notoriously poor, resulting in missed opportunities for empirical analysis and improvement, among other benefits. However, recent changes to the Common Rul...
Uloženo v:
| Vydáno v: | IRB |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5985974/ https://ncbi.nlm.nih.gov/pubmed/29881132 |
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