Successful DMF submissions Within One Week With 70% Cost Benefits

A South Korea based, global Pharma company, was filing information on APIs to the agency as cross reference to NDA and ANDA submissions. The DMF submissions required were for North America, Latin America and Canada. The major bottleneck to get through this project was to acquire sound knowledge on CA eCTD M1 specifications.

Download this case to get details on Freyr’s global delivery model for successful DMF submissions within one week. 

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