A Story of Transformation in Regulatory Submissions
Managing complex lifecycle submissions across multiple regions is no small feat. Tight deadlines, compliance pressures, and high stakes leave little room for error.
One global pharmaceutical leader faced these same challenges. Instead of reacting to every roadblock, they chose to be proactive—and partnered with Freyr SUBMIT PRO.
The Results? A Benchmark in Regulatory Excellence:
Seamlessly Imported and Validated Over 30 Sequences
Reduced manual intervention and submission bottlenecks.
Accelerated Submission Timelines by 10%
Freed up valuable team hours for strategic tasks.
Reduced Errors by 20%
Intelligent validation workflows minimized compliance risks.
Global Compliance Confidence
Aligned submissions with USFDA, EMA, MHRA, and other regulatory bodies.
Today, they’re not just meeting deadlines—they’re setting new standards for regulatory submission excellence.
Your team deserves the tools and technology
to excel in every submission.
Take the first step towards seamless, error-free, and
compliant submissions.
Trusted by Global Pharma Leaders
Who Submit Like Pros
Freyr SUBMIT PRO is the choice of industry-leading pharmaceutical enterprises,
helping them redefine regulatory success.
Our Clients Include:
Proven Results, Tangible Impact
25+
Presence Across 25+ Countries
100,0000+
Submissions Managed
450+
Regulatory Experts
3,350+
Active Users Globally