The National Institute for Health Research (NIHR), Clinical Research Network | 2012 | Source: The Guardian Volunteers involved with clinical trials are not human guinea pigs, but patients taking an active role in their healthcare, aiming to improve the quality… Continue reading
Ludman, E. J., Fullerton, S. M., Spangler, L., Trinidad, S. B., Fujii, M. M., Jarvik, G. P.,Burke, W. | Journal of Empirical Research on Human Research Ethics | September 2010 | NIH Public Access No consensus exists about when researchers… Continue reading
Singer, E., & Couper, M. P. | Journal of Empirical Research on Human Research Ethics | September 2010 | NIH Public Access For several years, we have experimented with various ways of communicating disclosure risk and harm to respondents in… Continue reading
Bhansali S., Shafiq N., Malhotra S., Pandhi P., Singh I., Venkateshan S. P., Siddhu S., Sharma Y. P., Talwar K. K. | Contemporary Clinical Trials | 2009 | NCBI-PubMed | Abstract The comprehension of informed consent is an integral part… Continue reading
David Wendler, Christine Grady | Bioethics | Vol. 22, Issue 4 | 31 July 2008 To give valid informed consent to participate in clinical research, potential participants should understand the risks, potential benefits, procedures, and alternatives. Potential participants also should… Continue reading
Ben Campbell | 2008 | Source: Dartmouth Ethics Institute | In the last decade, biomedical research conducted by researchers from developed countries in developing countries has been a topic of significant controversy. One serious concern is that research participants in… Continue reading
