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.