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Is an Investigational New Drug Application (IND) in your future? It’s an important development and regulatory milestone that requires thoughtful planning and expertise. It represents your opportunity to present the data and documents that support further investigation of your product in human trials.
- What is an IND?
- What's in an IND?
- How can you prepare for your first IND?
Your submissions to the FDA and all interactions with FDA review teams require thoughtful planning. Whether you have internal resources or are working with outsourcing partners, your "team" needs to be prepared to communicate efficiently and effectively.
This interactive program is designed for individuals and small teams who are or will be planning their first IND.
Join Dr. Lisa Jenkins VanLuvanee and the Facet Life Sciences team as we lead you down the home stretch, with valuable insights and practical experience to get you started.
Lunch will be provided for all attendees. Register above.
Facet is hosting another Lunch-N-Learn in June!
Topic: IND Stage Regulatory and Patent Analysis