The client was a USA-based multinational healthcare company who was looking for Regulatory support in filing MAA and baseline submissions to the USFDA. The project presented several challenges such as stringent timelines for filing high-quality submissions, tracking versions of frequently changed documents, and end-to-end publishing activities. Freyr’s talent pool was able to ensure timely submissions with zero errors and created a submissions e-roadmap for the future. The publishing activities were also carried out within the timelines with 100% accuracy rates.
Learn how Freyr worked against time and was able to make multiple submissions to the USFDA while taking care of end-to-end publishing activities for the client. Download the proven case.
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