Pricing built for regulated teams
Transparent, scalable pricing designed for medical device organizations. Start small, grow confidently, and keep compliance airtight at every stage.
Includes everything needed to standardize label data and ship faster.
- Unlimited projects, products, and label components
- Regulatory templates and symbol library access
- Version control with audit-ready change history
- CSV/PDF exports for downstream systems
- Email support with 1 business day response
Engage our team for compliance validation, security reviews, and integration scope.
Talk to Sales- Dedicated success and compliance onboarding
- Custom workflows, approvals, and RBAC
- Priority support and SLA options
- Security reviews, SSO, and audit support
- Integrations tailored to your tech stack
Optimized for medical device organizations
Use Uprevit to unify label data, approvals, and compliance evidence in one controlled workspace. Reduce regulatory risk while accelerating release cycles.
Built for FDA UDI, EU MDR, and global labeling rollouts.
Assemble label evidence, approvals, and audit trails in one workspace.
UDI Label Pack
EU MDR · FDA UDI
Symbols Library
ISO 15223-1
Change Review
Audit trail · QMS
Incorporate Uprevit in your QMS for audit-ready labeling documentation and traceability.
Pricing questions, answered
Clear, direct answers for regulated teams evaluating Uprevit pricing.
Align every label with global compliance in weeks, not months
See how Uprevit compresses labeling timelines while keeping regulatory confidence high across departments and geographies.