CMC Regulatory Workshop @ filings and how they relate to IP (WS10)

Date:
29 April 2019
Time:
-
Available Seats:
24

The CMC section of the IND contains information that has a direct influence on clinical trial supplies and failure to prepare IP that follows the requirements listed in that section can cause significant impact to a clinical trial.  This session will discuss the CMC information contained in a clinical trial regulatory filing and how it should be monitored to avoid issues wth clinical supplies.

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