Successful IND and NDA Submission to the USFDA

A U.S. based specialty pharmaceutical company was looking for Regulatory support in filing IND and NDA applications under strict timelines. The client was facing challenges with the submission of applications along with keeping track of all the revisions and their replacement in the eCTD format.

Through this case study, gain insights on how Freyr managed to file the applications without any errors and with 100% efficiency.

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