Freyr rDMS

Transform Document Management into a Strategic Advantage

Freyr rDMS Transform Document Management into a Strategic Advantage

Regulatory document management shouldn’t feel like an uphill battle. With Freyr rDMS, your team gets an intelligent platform designed to simplify workflows, enhance collaboration, and guarantee compliance. From document creation to global submissions, every step becomes smoother, faster, and smarter.

Accelerate Timelines, Amplify Outcomes

Time is critical in regulatory affairs. With Freyr rDMS, you’ll get documents out the door faster without sacrificing quality or compliance.

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Faster Approval Cycles
Error-Free
Document History
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Compliance Confidence
Global
Collaboration Across Team

Streamline Every Step,
Eliminate Every Bottleneck

Managing thousands of regulatory documents across regions and health authorities can quickly turn chaotic. Freyr rDMS eliminates inefficiencies by centralizing your documents, automating approvals, and ensuring every file meets regulatory standards before submission.

Centralized Access

All your regulatory documents, one secure platform.

Smart Workflows

Automate routine tasks and reduce manual errors.

Compliance by Design

Built-in validation tools keep you audit-ready at all times.

Collaborate Without Compromise, Anywhere, Anytime

Regulatory work doesn’t stop at office hours or office walls. Freyr rDMS ensures seamless collaboration across teams, regions, and time zones with tools designed for flexibility and precision.

Real-Time Collaboration

Review, comment, and approve documents simultaneously.

 

Secure Cloud Access

Work securely from anywhere with AWS-backed hosting.

 

Version Control Made Easy

Track every change with full visibility into document history.

 

Stay Audit-Ready, Stay Ahead of the Curve

Audits shouldn’t be stressful, they should be seamless. With Freyr rDMS, every document is tracked, validated, and ready for inspection.

Detailed Audit Trails

Complete transparency across every document action.

Flexibility in Import

Easily import pre-defined templates, ensuring seamless use and standardization.

Metadata Management

Tag and track documents for instant retrieval.

What Our Clients Say

Thank you, team, for your efforts in supporting several key launches over the last few months. Launches play a critical role in the growth of our business. Thank you to the entire team for your efforts and support in making our launches successful.

Director
Canada-based Global Generic Pharmaceutical Company

We use Freyr Submit Pro of Freyr Digital and find it user friendly. Also, their back-up team is very helpful in resolving technical problems. We get solutions at the earliest without affecting our submission timelines.

Product Development & Licensing Manager
A Leading Pharmaceutical Product and Service Provider

We are using Freyr’s products/services since 2016. It is very user-friendly and time to time updating as per Regulatory requirements and for software improvisation. Customer Support from Freyr is Very Satisfactory.

Deputy General Manager Regulatory Affairs
Leading Indian Pharma Company
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Empower Your Teams with Smarter 
Tools and Greater Confidence

When your team is equipped with the right tools, great things happen. Freyr rDMS is designed with teams in mind, ensuring everyone, from regulatory professionals to IT managers, can perform their best.

Regulatory Affairs Professionals

Simplify workflows and reduce time spent on approvals.

Compliance Experts

Ensure every document meets global health authority requirements.

IT Teams

Enjoy seamless integrations and zero installation headaches.


Your Next Submission Starts Here!

It’s time to leave behind fragmented systems, manual errors, and compliance headaches. With Freyr rDMS, every document contributes to your team’s success story.

Request a Demo