Ethical Issues in Clincial Trials, February 2000
Speaker's Outlines
•Donald Berry, Randomized Trials: When are they Ethical? When should they be stopped? When should they be repeated?
•Susan Ellenberg, The What, Why, and How of Clinical Trial Data Monitoring Committees •Harry Marks, Where Do Ethics Com From? The Role of Discipline and Institutions
•Charles Weijer, Clinical Equipoise and the Design of Randomized Clinical Trials •Tom Beauchamp, The nature of Informed Consent
•Jeremy Sugarman, Informed Consent in Special Populations
•Robert Levine, Recent Developments in the Ethics of Multinational Clinical Trials •Harold Kincaid, Outline of the Issues
Bibilography on Ethical Issues in Human Subject Research
•Belmont Report •Nuremberg Code •Helsinki Documentation •Federal Regulations •IRB Guidebook
A complete video including handouts of the conference, Ethical Issues in Clinical Trials is available for only $75. Send name, address, and check payable to UAB to: Harold Kincaid HB 423 900 13th Street South Birmingham, AL 35294-1260.
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