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- IMMPACT-XVIII Slide Presentations
- 1. A regulatory perspective on threats to the integrity of analgesic clinical trial efficacy data
- Sharon Hertz, MD
- 2. Clinical trial quality: what is it, and what approaches can optimize it?
- Nathaniel Katz, MD
- 3. Pain reporting: patient training, compliance, and monitoring
- Mark Jensen, PhD
- 4. Fabrication and concealment by clinical trial participants
- Eric Devine, PhD
- 5. Combating participant misbehavior in analgesic clinical trials
- Robert Dworkin, PhD
- 6. Evaluating and enhancing adherence to medications
- Bernard Vrijens, PhD
- 7. A regulatory perspective on electronic data capture
- Sarrit Kovacs, PhD
- 8. Site selection, training, and surveillance
- Richard Malamut, MD
- 9. Central statistical monitoring
- Amy Kirkwood, MSc
- 10. Data quality issues in the design and analysis of clinical trials: an FDA perspective
- Paul Schuette, PhD
- 11. An academic perspective on clinical trial quality
- John Markman, MD
- 12. Industry and CRO perspectives on clinical trial quality
- David Hewitt, MD