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Case Studies in Expediting Biologic Development

Summary: Biologic drug development is complex, requiring broad capabilities and expertise to ensure the highest likelihood of regulatory approval and commercial success.  The journey from cell line development to clinical trial supply can result in unforeseen issues that delay timelines or require additional resources. These added costs and delays can be detrimental to both sponsor companies and patients.

The webinar covers these challenges and tools for risk mitigation during biologic development and manufacturing, including case studies on how strategic partnerships and effective communication can result in reduced scheduling delays during drug substance development and expedited timelines between drug product filling and clinical trial supply.

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