See it on your own device in 10 minutes
Open the guided demo or book a walkthrough with our team.
Guided demo
A 12-step journey: company QMS backbone, first product dossier, gap closure and audit-ready exports.
Strong device description, partial risk & GSPR, draft IFU and Quality Manual — with deliberate gaps in biocompatibility, EO residual & sterilization validation, shelf-life, PMS/PMCF and 2 open CAPAs.
- 12 guided steps across QMS, technical file, consultant and exports
- Pre-loaded Yılmaz Bio scenario with deliberate gaps to explore
- Mark steps complete as you walk through the workflow
- Uses the same modules as production — not a separate mock UI
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