Zero Deficiency and Compliant IND Submissions to the USFDA

A U.S. based pharmaceutical product company was looking for assistance with filing IND applications to the USFDA. The client approached Freyr for support in filing quality submissions within given timelines. Freyr assisted the client to ensure compliant submissions for faster approval with zero error and warnings.

To know more about how Freyr managed to handle IND applications within stringent timelines, download the case study.

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