Successful Filing of DMF and Amendments in the USA

An India based leading manufacturer and exporter of pharmaceutical excipient was looking for filing DMF application and amendments as per the USFDA guidelines. Freyr provided the client assistance with submission of high quality DMF application within stipulated timelines with zero errors and warnings.

Decode the case study to understand how Freyr managed to accelerate the submissions for swift approvals with 100% accuracy.

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