Simplify Compliance for Medical Devices with the Power of AI
Schnell AI redefines regulatory compliance with agentic AI workflows, powering the next era of healthcare innovation.
The Problem
$500k
40 hours/week
40 hours/week
Medical device companies spend, on average, $500K to maintain regulatory compliance.
40 hours/week
40 hours/week
40 hours/week
Technical teams spend at least 40 hours per week manually compiling audit-ready documentation.
8 Months
40 hours/week
8 Months
The average time taken to file a pre-market submission (FDA 510(k), De Novo, Pre-market clearance) is 8 months.
Our Solution
Agentic Automation
On-premise Processing
Agentic Automation
Our AI Agents autonomously synthesize digital assets into audit-ready, compliant documentation, redefining regulatory workflows.
90% Time Reduction
On-premise Processing
Agentic Automation
Our solution saves more than 90% time required to maintain compliance.
On-premise Processing
On-premise Processing
On-premise Processing
All the data is processed locally or on-premise, maintaining data security and integrity.
How it Works
Our Partners
Contact Us
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