The client was a leading USA-based pharmaceutical company who was looking for Regulatory support in filing promotional labeling, amendments, meeting requests for the FDA, and DMF submission. The project came with multiple challenges, such as tracking versions of frequently changed documents, supporting end-to-end publishing activities, and filing the DMF submission within stringent timelines. Freyr provided full-time resources, ensured transparency throughout the publishing process, and filed a valid DMF submission with zero errors. Freyr’s talent pool was able to help the client meet their business objectives in the specified period.
Know more about how Freyr was able to make a timely DMF original submission and offered support in end-to-end publishing activities with zero warnings. Download the proven case.