Thursday, January 21, 2010
2:00 PM - 3:00 PM EST
About the webinar:
As the biotech and pharma industries come out of the current downturn, sponsors will increasingly look for lower coast, high quality cost solutions to their clinical data needs. Combine this with the ever decreasing availability and high cost of clinical trial patients in the US, and we find we must look to the emerging markets for our patients. Setting up studies in far flung places presents significant challenges to the sponsor and can put him in unfamiliar waters. This webinar will discuss ways in which sponsors might safely explore these markets to generate the clinical data they need efficiently and ethically.
What you will learn:
• Understanding the nuances of the changing regulatory environments in offshore clinical trials to better manage trial risks
• Know your environment: an up-to-date picture of standards in India and China and other regions
• Matching trials to the right country: evaluating trial requirements with different regulatory and environmental factors
• Choosing CRO’s that have credible and substantiated experience in trials with key groups
Presented by:
Jacquie Mardell
Sr Director Clinical Operations
Metabolex
Register here.
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