A French multinational pharmaceutical and healthcare company was looking for Regulatory support in submitting a response to a US FDA query. The project presented several challenges, such as:

  • Taking care of end-to-end publishing activities in defined timelines
  • Validating large volumes of documents using Agency-approved tools

Freyr’s team coordinated with the client and ensured transparency all around. A dedicated team of resources was able to file the submission successfully and ensure 100% quality, thus giving a competitive edge to the client.

For a detailed understanding of how Freyr's team met the client’s expectations and ensured that their business objectives were accomplished without any delays, download the proven case.