Freyr Digital Suite

Let’s talk about how Freyr Digital can accelerate your compliance, reduce risk, and drive strategic growth.

Discover Freyr Digital

Simplifying complex regulatory functions with software for life sciences companies - powered by 15+ years of hands-on regulatory services excellence.

0
of manual publishing efforts automated
0
time saved by publishers
0
reduction in artwork operation costs
0
cost savings on regulatory submissions
0
Users in 20+ countries
0
life sciences customers, from biotech to consumer health
0
total submission managed

Key Challenges & Our Solutions

Challenges
Freyr Digital Solutions
Lack of version control and audit-readiness in document management.
With Freyr rDMS you can effortlessly manage documents, control versions, track statuses, and maintain full audit trails — all in one place.
Manual, time-intensive eCTD submissions are prone to errors.
With Freyr SUBMIT PRO you can efficiently create, validate, and manage eCTD submissions.
Formatting complexities and validation requirements.
With Freyr SPL-SPM you can validate SPL files automatically with built-in checks that ensure full compliance with FDA formats and health authority guidelines.

Why Choose Freyr Digital

Proven Regulatory Heritage
Built on over a decade of hands-on global consulting experience and more than 100,000 submissions managed, our solutions embed industry best practices every step of the way.
Global Reach & Proven Adoption
Trusted by 200+ customers, 3,350+ users across 20+ countries, our solutions have been battle-tested in diverse regulatory environments.
Customer-Driven Customization
Our highly configurable workflows put your processes first, so you get a platform that adapts to your needs, not the other way around.
Flexible Deployment & Integration
Deploy on-premises, in your cloud, or hybrid-with an API-first architecture and legacy connectors to slot seamlessly into your enterprise ecosystem.

Core Modules & Top Features

Freyr SUBMIT PRO

Streamline your eCTD Submissions

  • Inbuilt eCTD validator & viewer
  • Supports all major eCTD templates
  • Deploy on-premises or in the cloud

Read More

Freyr rDMS

Enterprise-Grade Document Management

  • Version control & audit-ready traceability
  • Role-based access & advanced search
  • Collaborative authoring workflows

Read More

Freyr SPL-SPM

SPL (FDA) & SPM (HC) Content Management

  • Interactive dashboards & workflow management
  • Automated validation & submission
  • Advanced text comparison tools

Read More

Freyr Digital Helps…

01
Streamline Your eCTD Submissions
Streamlining submissions has never been easier. With our electronic Common Technical Document (eCTD) software, you can effortlessly assemble and submit your regulatory paperwork electronically, minimize manual errors, maintain adherence to electronic submission standards, and enhance the efficiency of your submission workflow.
02
Optimize Document Management
+
03
Streamline Your SPL-SPM Labeling & Monograph Management
+
04
Deliver Modular, Scalable Solutions
+
05
Deliver Solutions Purpose-Built for Life Sciences
+

Ready to Transform Your Regulatory Operations?

Request a Demo

How Does freya.docs Compare

Feature

  • Response Time
  • Ticket Cost
  • Support Model
  • Workflow flexibility
  • Deployment Options
  • Integration
  • Custom Reports & Dashboards
  • Compliance Certifications

  • 15 minutes
  • Free
  • Three-degree prioritization
  • Customer-driven, highly configurable
  • Cloud/On-Prem/Hybrid
  • API-first, legacy connectors
  • Included
  • ISO 27001, 21 CFR Part 11, GDPR-ready 

Other Providers

  • 24 hours
  • Charged per ticket
  • Ad-hoc, no prioritization
  • Tool-centric, fixed workflows
  • Usually single option
  • Limited or costly integrations
  • Premium add-ons
  • Varies; often extra charge