The customer is a global, generic pharmaceutical company and was looking for Regulatory support in delivering baseline submissions to the Saudi Food and Drug Authority (SFDA). The project presented several challenges, such as tracking versions of frequently changed documents and stringent timelines for delivering the submissions. Freyr created a detailed tracker to track all the version changes and validate them. Freyr offered end-to-end publishing support and got swift approvals for the submissions with zero defects.

Do you wish to know how Freyr made timely baseline submissions to the SFDA by creating a detailed tracking system and validating the voluminous documents? Download the proven case.