Wednesday, September 28, 2016 - Wednesday, November 16, 2016
Ethical and Regulatory Aspects of Clinical Research is a course offered by the Department of Bioethics at the NIH Clinical Center to anyone interested or involved in the ethics of clinical research with human subjects. Participants represent multiple disciplines including research teams, IRB members, physicians, psychologists, nurses, social workers, administrative staff, students, and others. Course Objectives By the end of this course, participants are able to: Utilize a systematic framework for evaluating the ethics of a clinical research protocol; Apply appropriate codes, regulations, and other documents governing the ethical conduct of human subject research to their own research; discuss controversial issues relating to human subject research, including Phase 1 research, randomization, children in research, international research, etc.; identify the critical elements of informed consent and strategies for implementing informed consent for clinical research; Describe the purpose, function, and challenges of IRBs; Appreciate the experience of human subjects who have participated in research protocols. The 2016 course will meet: Wednesdays, 8:30 - 11:30 AM. September 28 - November 16, 2016. For course materials, videocasts, past lectures, and more information, please visit http://www.bioethics.nih.gov/courses/index.shtml.
Wednesday, September 28, 2016 - Wednesday, November 16, 2016 8:30 AM - 11:30 AMEastern Time
National Institutes of HealthBldg 10, Lipsett Amphitheater10 Center DriveBethesda, Maryland 20892USA
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