A US-based leading pharma company that manufactures multiple excipients had to convert 17 DMF into eCTD format and further submit them to USFDA. The client approached Freyr for conversion of the DMF to eCTD and requested earlier delivery than the proposed timeline. Although Freyr face some business challenges but was able to successfully convert all the 17 DMF into eCTD and submitted them to the USFDA.

Read the case to know what technical inputs Freyr provided to the client for successful submission.

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