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.
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