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Go to market faster. Handle more submissions. Reduce rework.
Complizen equips large medtech organizations with a single, evidence-first platform that speeds time-to-market and strengthens every regulatory decision.
Cut through regulatory overload
Medtech teams lose critical time chasing documents, reconciling guidance changes, and repeating research across programs. Complizen centralizes FDA sources and delivers instant, cited answers, so your teams cut delays, strengthen submissions, and move devices forward faster.
Accelerating regulatory teams
Faster answers, stronger submissions, and fewer delays — Complizen equips enterprise regulatory teams to deliver results at scale.
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.”
Nathan Glass
CEO | Medlaunch
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.
5
minute onbaording
Teams get started instantly, with no complex setup.
Frequently Asked Questions
Answers on how Complizen helps you get clarity and speed to market.
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