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Clinical Trials (London, England)|August 3, 2017
Phase 1 healthy volunteer willingness to participate and enrollment preferencesStephanie C Chen, Ninet Sinaii, Gabriella Bedarida, et al.
Contemporary Clinical Trials|May 1, 2012
Randomization to standard and concise informed consent forms: development of evidence-based consent practicesMary E Enama, Zonghui Hu, Ingelise Gordon, et al.
Clinical Trials (London, England)|September 17, 2015
Considerations in the evaluation and determination of minimal risk in pragmatic clinical trialsJohn D Lantos, David Wendler, Edward Septimus, et al.
Critical Care Medicine|August 11, 2016
Targeted Consent for Research on Standard of Care Interventions in the Emergency SettingDavid Wendler, Neal W Dickert, Robert Silbergleit, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 20, 2006
Patients' decision-making process regarding participation in phase I oncology researchManish Agrawal, Christine Grady, Diane L Fairclough, et al.
AJOB Empirical Bioethics|June 11, 2019
Cancer Clinical Trial Patient-Participants' Perceptions about Provider Communication and Dropout IntentionsQiuping Zhou, Sarah J Ratcliffe, Christine Grady, et al.
Journal of Advanced Nursing|August 26, 2010
Everyday ethics: ethical issues and stress in nursing practiceConnie M Ulrich, Carol Taylor, Karen Soeken, et al.
Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health|January 15, 2013
Enrolling pregnant women: issues in clinical researchMary C Blehar, Catherine Spong, Christine Grady, et al.
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