A research-oriented pharmaceutical product development company based in India needed assistance with NeeS to eCTD conversions. Having faced numerous operational and technical challenges with the process of migrating and managing Regulatory dossiers, the client reached out to Freyr for a solution. Through integrating Freyr’s Regulatory software support and collaborating with specialized compliance team, the organization was able to streamline their end-to-end Regulatory operations including Document and Submission Level Publishing activities.

Download the proven case to learn how Freyr met the Regulatory criteria besides converting the documents within the timeframe.