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Covance to Present at the Drug Information Association's 45th Annual Meeting
Date:6/16/2009

| Speaker: Ross Rothmeier, senior director, EDC portfolio, clinical development services

June 23, 2009:

  • "Corrective Action and Preventive Action Program for Clinical Trial Programs"

8:00 a.m. | Session Chair: Bruce Wagman, MBA, RN, RAC, vice president, regulatory affairs and quality assurance, clinical development services

  • "Routine Monitoring Visits: Pragmatic Approaches to Reduce Prep Time by More Than 50%"

9:30 a.m. | Poster Presentation: Ann Flandermeyer, BSN, PhD, MSN, RN, project management and clinical operations

  • "Early Exposure to the Science of Safety Through Clinical Research in a CRO Setting for Future Medical Professionals"

9:30 a.m. | Poster Presentation: Jackie Miller-Giles, MT (ASCP), MS, global clinical pharmacology

  • "Nonclinical Support for First-in-Human Clinical Trials"

2:00 p.m. | Speaker: Paul Baldrick, PhD, head of department, pharmaceutical regulatory affairs

  • "Defining Quality in Clinical Trials (2nd Annual Update)"

2:00 p.m. | Session Chair: John Poland, PhD, senior director, regulatory policy, UK, clinical development services

  • "Changes in the WHO Review of Psychoactive Substances for International Control"

4:00 p.m. | Session Chair: Edgar Adams, ScD, MS, executive director, epidemiology, periapproval services

  • "Site Preferences for EDC - A Comparison of European and North American Perspectives"

4:00 p.m. | Session Chai
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SOURCE Covance Inc.
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