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EMPIRICAL EVALUATION OF THE NEED FOR ‘ON-GOING CONSENT’ IN CLINICAL RESEARCH
OBJECTIVE: Some commentators argue that informed consent for clinical research should be an on-going process, which begins, rather than ends, with participants’ initial consent. Lacking, however, are empirical data on whether there is a need for ‘on-going consent’. DESIGN: Two self-administered surv...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2995831/ https://ncbi.nlm.nih.gov/pubmed/21076272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/QAD.0b013e328340fec7 |
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