##  [Successful Type III DMF Compilation and eCTD Submission to USFDA](/index%2ephp/case-studies/successful-type-iii-dmf-compilation-and-ectd-submission-to-usfda) 

- [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)

 

 ![Successful Type III DMF Compilation and eCTD Submission to USFDA]()

A US Based custom and standard glass products manufacturing company was looking for Regulatory assistance for compilation and submission of Type III DMF in eCTD format, as per the USFDA regulations. The objective was to make the submissions on time as the client was novice to the eCTD format.

Download the case to know how Freyr managed to complete the eCTD submissions in the given stipulated timeline to the USFDA.



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