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
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