Fast-tracked Drug Development in Just 37 Weeks

A Rapid & Robust IND-enabling Package

Learn how Evotec's INDiGO^® solution allowed a small US biotech to rapidly and efficiently achieve regulatory submission of their key asset in just 37 weeks.

Key points in our case study:

• A robust regulatory data package was delivered ahead of schedule and within budget
• Evotec’s integrated approach ensured rapid decision-making and careful risk management
• Thanks to the application of the team’s scientific knowledge and regulatory awareness, the asset was quickly approved and entered clinical development

How can you ensure a rapid and robust IND-enabling package that minimizes risk and delivers results in the shortest possible timeframe?

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