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Evidence
Generate EU MDR-ready documents in minutes — directly in your browser. One unified workspace for Post-Market Surveillance, Regulatory Affairs, and Clinical teams.
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Quantify & synthesize complaint + clinical data. Track your entire medical device portfolio in real time.
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Automated harmonization, compliance rules, and formatting — everything stays MDR-ready without effort.
Evidence
Your single source of truth. All clinical, regulatory, and PMS data in one secure, audit-ready platform.
Simple, Transparent Pricing
One price. No hidden fees. Cancel anytime.
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Individual
$TBD/month
$TBD / year (2 months free)
For consultants & solo professionals
- Unlimited document creation
- Full clinical data workspace
- Secure storage & version history
- Email support
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Organization
$TBD/month
$TBD / year (2+ months free)
For growing medtech teams
- Everything in Individual
- Multi-user workspace & permissions
- Shared environment
- Priority support
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Professional Services
$TBD/hour
Need a little (or a lot) of help?
- Custom template development
- Legacy data migration
- Onboarding & team training
- Use case consulting
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