A Swiss multinational pharmaceutical approached Freyr for assistance with submitting detailed information in NeeS and eCTD format in multiple region. The challenge was to understand the Regulatory requirements of multiple regions and comply with them while submitting multiple high-quality INDs, ANDAs, MAAs, and NDAs. Freyr managed to support the client by deploying a 24x7 support system to ensure successful submissions with increased cost benefits.

Download the case study to know how Freyr supported the client with 8000+ submissions.