February 19, 2019
Date: Feb 19, 2019
Duration: 20 Min
Sponsored by Catalent
This webcast features: Kristen DeVito, Global Director, Clinical Supply Services, Catalent Pharma Solutions
Biologic clinical trials can be complex with many factors to consider. Understanding your specific needs and developing a plan early on during drug development can reduce delays and missteps during clinical trials. This presentation will discuss:
How protocol design can impact clinical supply strategy
Which clinical supply variables are most likely to be on the critical path
Proactive steps to ensure continuity of supply and reduce the risk of study delays and budget overruns
Watch the recorded webcast below.
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