##  [Compliant IND Submissions to the USFDA with Quick TAT](/index%2Ephp/case-studies/compliant-ind-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)

 

 ![Compliant IND Submissions to the USFDA with Quick TAT]()

A U.S. based company with specialization in anti-infective drugs was looking for Regulatory support in filing IND application. The challenge was to accelerate the delivery time of the applications as the timeline were stringent. Freyr assisted the client with the submission of IND applications within the stipulated short timeline while maintaining the quality of the applications.

Download the case study to decode how Freyr managed to deliver compliant and error-free IND applications with 100% accuracy.



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