A UK based pharmaceutical company was looking for Regulatory support for submission of original NDA application to the USFDA. The scope of the project was to understand and meet the Regulatory requirements of the Agency and align with them. Freyr assisted the client with the submissions by providing 24x7 Regulatory support in quick TAT.
Download the case study to decode how Freyr provided end-to-end publishing services and managed to increase the cost benefits up by 70%.
Fill the form below to download the Case Study
