Jaime Lazovski, Marcelo Losso, Benjamin Krohmal, Ezekiel J. Emanuel, Christine Grady, David Wendler | Journal of Empirical Research on Human Research Ethics | September 2009 | Source: NCBI-PubMed Abstract Systematic data on the impact that longitudinal clinical trials have on… 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
Adriana Petryna | Princeton University Press | 2009 The phenomenal growth of global pharmaceutical sales and the quest for innovation are driving an unprecedented search for human test subjects, particularly in middle- and low-income countries. Our hope for medical progress… Continue reading
Richard S. Saver | Western New England Law Review | Volume 31, Issue 2 | 2009 Medical research subjects increasingly are demanding (and litigating about) continued access to investigational technology after the clinical trial has concluded. The Article undertakes a… Continue reading
Thatte U. M., Bavdekar S. B. | Journal of Post Graduate Medicine | October – December 2008 | Source: NCBI-PubMed Abstract India is considered as a preferred site for conducting global clinical trials. Existence of a large treatment-naïve population, availability… Continue reading
Doris Shroeder | RECIIS – Elec. J. Commun. Inf. Innov. Health. Rio de Janeiro, v.2, Sup. 1, p.Sup.63-Sup.73, Dec., 2008 In its essence, post-trial obligations describe a duty by research sponsors to provide a successfully tested drug to research participants… Continue reading
