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Many regulatory software solutions have served their purpose, but as the industry evolves, so should your tools. Freyr SUBMIT PRO is designed to not just meet but exceed the expectations of modern regulatory affairs professionals, offering the most advanced features on the market today.

If you're using a platform that feels outdated or lacks the necessary support for future growth, it might be time to consider an upgrade. Freyr SUBMIT PRO provides the innovative tools you need to stay ahead, with a clear focus on efficiency, compliance, and ease of use.

Key FeaturesFreyr SUBMIT PROCompetitor Solutions
Integrated Document Management System

 

 

 

eCTD v4.0 (RPS) Readiness

 

 

 

Hyperlink Management

 

 

 

NeeS and ASEAN Support

 

 

 

Paper to Digital Migration

 

 

 

Training 

 

 

 

DLP Capablitites

 

 

 

Content Authoring templates

 

 

 

After Sales Service

 

 

 

User Friendly

 

 

 

Security

 

 

 

Tech Support

 

 

 

3350+ Users 
Enhancing Their Regulatory Journey 
With Freyr Digital.

TADs
Sigachi
Regulatory-Services
Pharma
Neo
Mingtai
Ligand
IVC
Fleming-labs
Bonifarm
Ambicare
Suven Pharma
Sun Pharma
Creative Pharma
Virupaksha
Tyche
Micro Labs Limited
Himalaya
Sparc
Otsuka
Cipla

The All-in-One Regulatory Solution That Your 
Existing Software Couldn't Deliver!

When Good Isn't Enough, Choose Great 
Why Freyr SUBMIT PRO Stands Out

Streamline your submissions with our integrated Document Management System (DMS), designed to handle everything from document storage to regulatory compliance with ease.

Freyr SUBMIT PRO includes an eValidator that aligns with the latest regulatory standards, ensuring your submissions are always compliant.

Keep your submissions flawless with our advanced link management features that ensure all links are accurate and functional.

Easily migrate from your existing software to Freyr SUBMIT PRO with our robust tools that automate and simplify the transition.

Freyr SUBMIT PRO supports a wide range of dossier formats, including NeeS and ASEAN, ensuring you can work with any format your submission requires.

Our platform includes thorough eCTD training to keep your team up-to-date, along with ongoing support to address any challenges you may face.
Make Your Regulatory Submissions Seamless

Regions We Cover

Freyr SUBMIT PRO supports global submissions in regions such as the Health Authority regulations in North America – US, Europe, Health Canada, Switzerland, Australia, Middle East, including GCC, Jordan, and Asia, including Thailand, South Africa, EAEU and ASEAN supporting a diverse range of submission templates and formats ensuring that your products meet regulatory requirements worldwide.

Extensive Training and Support

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What Our Clients Are Saying

 

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
 

Freyr Submit Pro software is user friendly and easy to use for submission of DMF to the Regulatory authorities like US, and EP.

Senior Manager Corporate QA & RA
Largest manufacturers of Microcrystalline Cellulose worldwide
 

We are using Freyr SUBMIT PRO 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