The client was a Hungarian research and development pharmaceutical company and was looking for Regulatory support in the filing of response and making amendments to the original submissions made to the USFDA and Health Canada. The project came with several challenges like tracking versions of frequently changed documents and stringent timelines. Freyr validated the documents and helped in granular Document Level Publishing (DLP). The experienced resources at Freyr were able to create a tracker that helped the client in the LCM activities.
Decode how Freyr was able to meet all the deadlines set by the client and ensured zero defects in the submissions by maintaining a complaint Regulatory pathway. Download the proven case.