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

r: Eunice Franklin-Becker, MPH, senior project manager, registries and observational studies, periapproval services

  • "First-In-Human Trial Designs: How Much is Too Much?"

4:00 p.m. | Session Chair: Mary Westrick, PhD, global vice president and general manager, clinical pharmacology

June 24, 2009:

  • "Six Sigma: How to Leverage 'A Great Idea' in the Complex Reality of Clinical Trials"

8:30 a.m. | Session Chair: Tim G. Strauss, MA, executive director, business process improvement, clinical development services

  • "Outsourced Data Management: How to Align Performance Expectations"

10:30 a.m. | Session Chair: Mark Anderson, senior director, data management, clinical development services

  • "Site Activation: How to Get Beyond the Classic Pitfalls"

1:30 p.m. | Speaker: Heather Almonte, MBA, RAC, senior manager, site activation, clinical development services

  • "An Overview of Challenges and Strategies to Make Remote Investigator Training a Reality"

3:30 p.m. | Speaker: Christina Werremeyer, project manager, periapproval services

  • "Latin America: Leveraging Regional Strengths While Proactively Ensuring Quality"

3:30 p.m. | Session Chair: Katie Margules, PharmD, MSc, senior director, clinical development services, Latin America

June 25, 2009:

  • "Proactive Management of Project Financials: Understand Scope of Work, Cost to Complete, and Scope Change"

8:30 a.m. | Ses
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SOURCE Covance Inc.
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