Preparation, and Submission of IND

Freyr assisted a US-based client in submitting its IND to the United States Food and Drug Administration (US FDA) for its specialized product.

The company lacked experience and had a limited understanding of filing a proper IND application for its product. With adequate support from Freyr, the IND was reviewed, expert advice was provided on the gaps, and the IND was submitted.

Download the proven case to learn how Freyr’s RA team assisted in filing IND for a US-based company.

Fill the form below to download the Case Study