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The top documents tagged [subjects participation]
French Nutrition and Health Survey 2006 - 2007 (Etude Nationale Nutrition Santé ENNS 2006 – 2007) French Institute for Public Health Surveillance
221 views
New IRB Policies Reporting Unanticipated Problems & Adverse Events Data & Safety Monitoring Susan Burner Bankowski, M.S., J.D. Chair, OHSU IRB
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COMMON PROBLEMS IN INFORMED CONSENT Jeri R. Barney, JD, MS Michele Antisdel, MBA/CCRP HRPP Compliance ManagerIRB Regulatory Analyst Human Research Protection
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Ny Presbyterian Quality Symposium
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Cox Regression
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Medical Billing Compliance Clinical Trial Billing Audits at Yale: Processes and Findings November 10, 2011
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INFORMED CONSENT: PROCESS, DOCUMENTATION, ALTERATION AND WAIVERS Suzanne Sparrow
217 views
Research Ethics The American Psychological Association Guidelines Protecting the Welfare of Animal Subjects Fraud in Science Plagiarism Ethical Reports
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Columbia University Medical Center Research Billing Compliance presented by Office for Billing Compliance Research Billing Compliance presented by Office
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1 Writing Better Consent Forms Rick Wagner Associate Director Human Research Protection Program
[email protected]
218 views
Agenda Objective: 1.To understand the ethical obligations of researchers with human subjects. 2.To understand the questionable history of human subjects
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Informed Consent UTHSC Institutional Review Board (IRB)
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