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Device Classification Wizard — Classify Your Medical Device Under EU MDR and FDA

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Book a 30-minute demo, or request a 14-day trial of the core QMS. Plans from EUR 49/month plus the Core QMS base, excl. VAT.

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MoniDoseQMS

The eQMS for medical device companies, with regulatory experts connected and a notified-body workspace (pilot programme open). 130+ modules, EU-hosted SaaS.

Monidose Oy (Y-tunnus: 3478744-6)

Turuntie 3, 37830 Akaa, Finland

info@monidoseqms.com

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Supports:ISO 13485EU MDRFDA QMSRISO 14971IEC 62304EU AI Act

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