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Use of altered informed consent in pragmatic clinical research
There are situations in which the requirement to obtain conventional written informed consent can impose significant or even insurmountable barriers to conducting pragmatic clinical research, including some comparative effectiveness studies and cluster-randomized trials. Although certain federal reg...
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| Vydáno v: | Clin Trials |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4688909/ https://ncbi.nlm.nih.gov/pubmed/26374677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1740774515597688 |
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