A U.S. based company specialized in glass vials/ampoules was looking for Regulatory assistance for submission of DMF application. The challenge was to file the DMF application along with handling a large volume of documents in a definite period. Freyr, with a dedicated team of full-time resources, assisted the client with timely submission of the application.
To know more about how Freyr managed to handle DMF submissions for the USFDA, download the case study.
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