Trusted by 3,350+ Users


















Quick Comparison
Feature | freya fusion | Other Providers |
---|---|---|
Response Time | 15 minutes | 24 hours |
Ticket Cost | Free | Charged per ticket |
Support Model | Three-degree prioritization | Ad-hoc, no prioritization |
Workflow Flexibility | Customer-driven, highly configurable | Tool-centric, fixed workflows |
Deployment Options | Cloud/On-Prem/Hybrid | Usually single option |
Integration | API-first, legacy connectors | Limited or costly integrations |
Custom Reports & Dashboards | Included | Premium add-ons |
Compliance Certifications | ISO 27001, 21 CFR Part 11, GDPR-ready | Varies; often extra charge |
The Challenge: Why You’re Frustrated
Our last vendor took 24 hours to respond,
charged for every ticket, and forced us into rigid workflows.
Waiting up to 24 hours for a support reply leads to critical delays in submissions and approvals.
Every fix incurs extra fees—inflate your budget unpredictably.
You’re forced to adapt to their system — instead of using a platform that adapts to your needs and processes.
Our Three-Degree Support Model
We believe support shouldn’t be an afterthought — or a chargeable service.
Freyr offers always-included premium support, built to serve life-science teams under pressure.
Auto-Escalation & Triage:
Tickets auto-route to the right expert within 15 minutes.
Dedicated Account Manager:
Personalized oversight, weekly check-ins, rapid root-cause identification.
Continuous Improvement Loop:
Post-ticket analysis, feedback integration, and platform enhancements.
Flexible Pricing Plans with no hidden costs
Whether you’re a small business or a large enterprise, we have a plan that fits your budget. No hidden fees, just transparent pricing that meets your needs.
Our Solutions
Explore our suite of regulatory tools - purpose built to accelerate compliance, minimize manual effort, and give you unmatched control.
Accelerated Regulatory Submissions with AI: Plan, compile, validate, and track global submissions end-to-end in a single, cloud-native platform-ensuring consistency, confidence, and complete control throughout the submission lifecycle.
Purpose-Built Regulatory Document Management: A 21 CFR Part 11- and GxP-compliant cloud-native DMS that delivers secure signatures, audit trails, validated workflows, and metadata-driven automation for inspection-ready, end-to-end content management.
Global Registration & Lifecycle Intelligence: Centralize tracking of products, applications, licenses, and lifecycle events across all markets-automatically monitor renewals, variations, and approvals in one streamlined, customizable system.