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Evidence-first regulatory research
Built for consulting firms, Complizen turns weeks of regulatory research into minutes — with every answer traceable back to its sources. Faster outputs, without sacrificing proof.
Minimize busywork,
Maximize outcomes
Manual research, and fragmented tools delays client impact. Here's how Complizen changes that.
Measurable impact for your team
Independent consultants and large firms alike are saving time, improving accuracy, and delivering more with Complizen.
Data security by design
Built with security at every layer, from infrastructure to application, ensuring your sensitive medical device data remains protected.
Private AI
Customer data is never used to train AI models — your information remains yours.
Compliance By Design
Our platform is architected with regulatory best practices (SOC2) at the core.
End-to-end encryption
All customer data is encrypted in transit and at rest with industry-standard AES-256.
Audit Ready
Every action is logged for traceability and compliance support.
“What used to take weeks of digging now takes minutes with Complizen.”
Leah Gustke
RA/QA Specialist | Exodus New Ventures
Resources to accelerate your journey
Expert insights, practical guides, and industry best practices from our team of regulatory professionals.
12+
hours saved weekly
Time teams save on regulatory research.
96%
pro-code accuracy
AI-driven classification validated against FDA records.
80%
faster predicate search
Relevant predicates identified and compared in minutes.
3x
more client capacity
Deliver more projects with the same team size.
Frequently Asked Questions
Answers on how Complizen helps you get clarity and speed to market.
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