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AI That Works Where You Work

From submission teams to CRO partners, Amia builds AI that fits your regulatory workflow.

Pharma & Biotech

Specialized services for R&D, regulatory affairs, and medical writing teams.

medical devices

AI-Powered Automation for 510(k), PMA, and DHF Submissions Accelerate FDA Clearance with Confidence.

Diagnostics

Generate Analytical and Clinical Validation Reports for 510(k) and PMA with AI Precision

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Featured Case Studies

How MedNova reduced New Drug Application (NDA) submission prep time by 40%?
How can Mednova generate your Clinical Study Reports in days—not months—usi...
Accelerate IND/NDA Submissions with AI Agents.

Customize

How We Customize
by Industry

Regulatory-aware

Domain-trained LLMs with ICH and FDA language baked in

Versatile

Deployed on secure cloud or On-Prem environments

Accelerated

Pilots launched in <30 days with minimal IT lift

Not sure which solution fits your team?