##  [Zero Deficiency Submissions to the USFDA with Quick TAT](/index%2ephp/case-studies/zero-deficiency-submissions-to-the-usfda-with-quick-tat) 

- [Medicinal Products](/index%2ephp/case-studies-main-categories/medicinal-products)
- [Publishing and Submission](/index%2ephp/case-studies-main-categories/publishing-and-submission)





[US FDA](/index%2ephp/case-studies-heath-authority/us-fda)

 

 ![Zero Deficiency Submissions to the USFDA with Quick TAT]()

A China based pharmaceutical company was aiming to file compliant DMF application as per the guidelines of the USFDA. The client was facing challenges in understanding the requirements of the Agency along with tracking all the revisions. The company approached Freyr for assistance with the submissions.

Download the case study and decode how Freyr provided the client with zero deficient and timely submissions.



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