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Discover how a leading Japan-based pharmaceutical company transformed its global regulatory publishing and submissions with Freyr’s end-to-end solutions. Facing challenges such as complex submission formats, tight deadlines, and multi-region compliance requirements, the client turned to Freyr to enhance accuracy, efficiency, and scalability.
With Freyr’s automation-first approach, dedicated publishing experts, and 24/7 global delivery support, the company achieved 40% automation, 50% reduction in manual effort, and zero-delivered defects across 35+ countries. Leveraging integrated tools and streamlined workflows, Freyr enabled over 15,000 successful submissions to global health authorities including PMDA, FDA, and EMA.
The result — faster submissions, consistent compliance, and sustainable operational excellence.
Download the case study to see how Freyr helped a global pharma leader simplify publishing, accelerate timelines, and achieve flawless submissions.
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