ProductUpdated on 26 February 2025
What we do?
About
meddevo helps you cut your regulatory burden by more than 50% by automating technical documentation and digitalizing regulatory affairs processes. All in one ...
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
Organisation
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