Investigator Initiated Trials: Challenges in Supporting

20 October 2016
Available Seats:

The attendee will be able to:
(1) Identify at least two (2) regulatory hurdles that must be overcome when conducting global IITs
(2) List two (2) things that a clinical supplies project manager must keep track of and control when conducting IITs
(3) Compare and contrast the clinical supplies requirements between standard clinical trials and IITs

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