Reforming the regulations governing research with human subjects.
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[1] Michael K Paasche-Orlow,et al. Readability standards for informed-consent forms as compared with actual readability. , 2003, The New England journal of medicine.
[2] P. Appelbaum,et al. The evolution of consent forms for research: a quarter century of changes. , 2010, IRB.
[3] Laura Lyman Rodriguez,et al. Responsible Research: A Systems Approach to Protecting Research Participants , 2003 .
[4] C. Grady,et al. Oversight of Human Participants Research: Identifying Problems To Evaluate Reform Proposals , 2004, Annals of Internal Medicine.
[5] P. Ubel,et al. Pruning the regulatory tree , 2009, Nature.
[6] Roger T. Anderson,et al. Variations among Institutional Review Board reviews in a multisite health services research study. , 2005, Health services research.
[7] Seema K. Shah,et al. How do institutional review boards apply the federal risk and benefit standards for pediatric research? , 2004, JAMA.
[8] J. Stockman. Funding of US Biomedical Research, 2003-2008 , 2011 .
[9] S. Hull,et al. Variability among institutional review boards’ decisions within the context of a multicenter trial , 2001, Critical care medicine.