Ethical and Regulatory Aspects of Clinical Research Lectures
Presentation Slides for 2008 course
NB: Instructions on how to print multiple slides on one sheet of paper from the pdfs below are available.
- What Makes Clinical Research Ethical? presented by Ezekiel Emanuel
- History, Scandals and Tragedies: Beecher, Tuskegee, Willowbrook and the Rest presented by Susan Lederer
- Do the Codes Apply to My Research? presented by Christine Grady
- Purpose and Function of IRBs: Successes and Current Challenges presented by Jerry Menikoff
- Coercion and Undue Inducement in Research presented by Alan Wertheimer
- Fair Subject Selection and Vulnerability presented by Dave Wendler
- Conflict of Interest and Clinical Re$earch presented by Cary Gross
- Ethics of Phase I Research presented by Ezekiel Emanuel
- Ethical Conflicts in Randomized Controlled Trials presented by Robert Truog
- Ethics of Placebo-Controlled Trials presented by Franklin Miller
- Ethical Issues in Research with Children presented by Lainie Friedman Ross
- Mock IRB presented by Christine Grady
- Evaluating Risks and Benefits of Clinical Research presented by David Wendler
- Research Involving Persons at Risk for Impaired Decisionmaking presented by Donald Rosenstein
- The Quality of Informed Consent: What do the data show? presented by Christine Grady
- Informed Consent presented by Seema Shah
- Exploitation in Clinical Research presented by Alan Wertheimer
- International Research: Trial Design Issues and Outsourcing presented by Reidar Lie
- International Research Ethics presented by Seema Shah
- Ethical Issues in the Use of Stored Samples presented by Sara Chandros Hull
- Ethical Issues in Genetics Research presented by Benjamin Wilfond
- Genetic Research in the Aka Pygmy people presented by Christine Grady
