Freyr SUBMIT PRO

Be Proactive. Be Productive. Be a Pro in Submissions.

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Freyr SUBMIT PRO Be Proactive. Be Productive. Be a Pro in Submissions.

In the world of global regulatory submissions, precision isn’t optional, it’s everything. Freyr SUBMIT PRO empowers your team to handle complex submissions with ease, speed, and confidence. Whether you're managing a single regional submission or orchestrating a global rollout, this tool transforms your team into submission pros.

Client Insights
Clients rated Freyr’s Quality of Service Deliverables an average score of
4/5
Client Insights
Customer Query Response received an average score of
4.5/5

What is Freyr SUBMIT PRO

Freyr SUBMIT PRO is a next-generation submission management software designed to streamline, simplify, and supercharge your regulatory workflows. Built specifically for pharmaceutical regulatory affairs teams, it combines automation, intuitive design, and industry-best practices to ensure your submissions are always compliant, always on time, and always professional.
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Faster Submission Timelines
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Fewer Submission Errors
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Lower Operational Costs
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Successful Global Submissions
Zero
Recalls in the Last Decade
Freyr Submit Pro Image

Why Choose Freyr SUBMIT PRO

Proactive Compliance
Stay ahead of changing regulatory requirements with built-in templates for FDA, EMA, TGA, and more.
Pro-Level Validation
Eliminate errors with an integrated eCTD validator and viewer - no third-party tools required.
Proven Automation
Cut manual effort with sequence cloning, application cloning, and smart metadata handling.
Pro Performance Dashboard
Track every submission in real-time with an intuitive dashboard packed with actionable insights.
Pro Anywhere, Anytime
Access Freyr SUBMIT PRO from anywhere in the world with just a browser and credentials using a secure and cloud-hosted platform.

Spotlight Features That Put the 'Pro' in 
SUBMIT PRO

Global Health Authority Templates

Ready-to-use templates for seamless submissions across regions.

AI-Enabled Automation

Intelligent workflows that predict errors before they happen.

Built-in eCTD Viewer & Validator

One platform, zero reliance on third-party tools.

Seamless Integrations

Connect effortlessly with DMS platforms like Veeva Vault and Documentum.

Audit-Ready Tracking

Detailed version history and robust metadata controls.

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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Built for Every Pro
in Your Team

Whether you're a small team aiming for precision or a global giant scaling compliance workflows, Freyr SUBMIT PRO adapts to your needs.

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Regulatory Publishers

Fast, error-free submission creation and validation.

Compliance Teams

Peace of mind with built-in checks and compliance reporting.

IT Teams

Hassle-free integrations, cloud security, and zero installation worries.


Ready to Submit Like a Pro?

When It Comes to Regulatory Submissions, Be the Pro You Were Meant to Be.

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