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Assyro:Accelerate Drug Submissions , Reduce Risk, and Cut Costly Rework with an AI Regulatory Copilot

Draft 3× Faster. Validate in Half the Time. Submit Without Rework. Your AI regulatory copilot with clause-level intelligence, real-time eCTD validation, and audit-ready trails for drugs and biologics

Assyro

Assyro AI is an AI-powered regulatory copilot designed to transform how pharmaceutical and biotech companies prepare and submit regulatory documentation. By combining advanced drafting assistance, real-time eCTD/RPS validation, and deep regulatory intelligence, Assyro helps teams accelerate submission timelines, minimize compliance risk, and reduce costly rework. Its platform delivers clause-level guidance and audit-ready trails tailored for drugs and biologics, enabling regulatory, publishing, and compliance leaders to draft faster, validate more efficiently, and submit with confidence.

Assyro gives regulatory teams a secure, AI-native way to move from manual, error-prone submission workflows to faster, data-driven operations that are always inspection ready. By combining clause-level regulatory intelligence with high-speed, local eCTD validation and transparent audit trails, it helps pharma and biotech organizations accelerate approvals, reduce compliance risk, and scale global submissions without adding headcount.