Everything You Need To Know About Investigational New Drug Applications (INDs)

Get the infographic that answers the top 5 frequently asked questions about investigational new drug applications (INDs).

Drug developers looking to bring their therapies into human clinical testing in the United States must file an IND with the United States Food & Drug Administration (FDA). But why?

Veristat regulatory experts have compiled the answers to these top 5 questions they get asked often:   

  1. What is the purpose of the IND?

  2. What are the 3 Types of INDs?

  3. What is the format of an IND?

  4. What the FDA really cares about in your IND?

  5. How does the FDA approve the IND?
Get the infographic that answers these 5 questions by completing the form on this page's right-hand side.