Fast Track Phase 1 studies: Shortening timelines to 1 month

20 October 2016
Available Seats:

The attendee will be able to:
1.) Determine no less than two (2) ways to shorten Phase 1 studies through increased efficiencies in clinical supplies management
2.) Explain the reason why shortening phase I trials has become such a high priority in drug development
3.) Differentiate between standard Phase I clinical trial requirements and Fast Track Phase I clinical trial requirements

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