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Saturday, January 19, 2008


Free Webinar: China Clinical Supply Logistics

Co-Hosted by World Courier and Merck

Tuesday, February 12, 2007 | 10 - 11 am (EST)

China has long been considered a potential clinical trials mecca due to its massive patient population, cost-effective investigator sites and an expanding presence of qualified contract research organizations. However, regulatory hurdles, logistical complexities and governmental instability has historically discouraged much focus on China from the pharmaceutical and biotech sectors.

Times have changed! Currently an unprecedented number of new studies are being planned and conducted in China. Nevertheless, many challenges still exist and must be overcome in order to ensure clinical trial investments are not negated by regulatory burdens.

This webinar will provide an overview of:

Yes Important Feature The clinical trial approval process in China
Yes Important Feature Import procedures for investigational drugs
Yes Important FeatureUnique logistical and cold chain challenges

Our knowledgeable speakers have years of regulatory and logistical experience in emerging countries, including China.


Frank Reale
Associate Director
Worldwide Regulatory Coordination & Clinical Supplies

Merck Research Laboratories

Mike Sweeney
Global Director of Strategic Development
World Courier, Inc.

To register for this free webinar Click Here.

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