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Automate your Technical Documentation

Regulatory End-to-End Process. From Data to Submission.
Single Source of Truth, no Redundancies, Re-Useable Data
Intelligent Documents and Auto-Updates
Automated Submission structures: EU-MDR, FDA, etc.
Monitoring of Data, Documents and Submissions
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Sync your Quality with eTD

Run Changes, CAPA, Complaints and Custom Processes directly in the system.
Gain maximum Insight due to full eQMS and eTD sync.
Decrease process time and administrative burden to a minimum.
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Take a look at the most sophisticated solution developed specifically for medical devices.
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