Global Comparator Studies

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Expedite Your Clinical Trials To Reduce Costs & Maximize Profit

The globalization of clinical trials has arrived. As you know, the increasing use of comparator studies means that you’re playing by a new set of rules. At this critical junction, you can either evolve in 2009 to stay ahead of the curve or choose to play catch-up and try to deal with the challenges as they arise.

The Global Congress on Comparator Studies gives you the unique opportunity to get ahead of the industry and establish your strategy for sourcing comparators and overcoming regulatory challenges in just two days. Imagine having a comprehensive blueprint for your comparator studies by the end of July?


2009 SPEAKING FACULTY INCLUDES:
Frank Reale
Associate Director
Worldwide Regulatory
Coordination and
Clinical Supplies Merck
Micheline Marshall
Director, Clinical Pharmacy Wyeth
Lorna Briddick
Global Clinical Supplies
Regional Lead, Latin America
Schering Plough Corporation
David Bernstein, Ph.D.
Principal Consultant
Bernstein CMC
Regulatory Consulting
Anthony Figazzotto
Acting Director, Global Supply Operations
GlaxoSmithKline
Lisa Ortega
Manager, Investigational Supply Planning & Logistics
Allergan

INTERACTIVE COMPARATOR WORKSHOP
“What can a clinical trial executive do to ensure their comparator studies in India are going to meet regulatory expectations?”
“When should I use single source? What if there are changes to the trial along the way?”
Regulatory Overview:
Exploring Regulatory Barriers and the Impact on Comparator Studies

Methods for Finding Common Ground:

Balancing Supply Concerns with Regulatory Requirements
GLOBAL CONGRESS BLOG

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