Blogs

Recent Blog

2 min read
Health Canada's July 2025 XML PM Mandate Explained
April 25, 2025
Freyr SPL - SPM

Key Updates on TGA’s eCTD 4.0 Rollout
April 18, 2025
Freyr SUBMIT PRO

3 min read
Global Regulatory Harmonization Efforts in 2025
April 11, 2025
Freyr SUBMIT PRO

3 min read
Navigating FDA’s New Accelerated Approval Guidance
March 28, 2025
Freyr Digital

3 min read

1 min read
May 31, 2023
Freyr Digital,
Freyr Artwork 360
Importance of Getting Artwork Right-First-Time: A Guide to Artwork Management
2 min read
May 12, 2023
Freyr Digital,
Freyr SUBMIT PRO
Navigating Regulatory Submission Hurdles:
Tips for Small & Midsize Life Sciences Businesses
2 min read
April 20, 2023
Freyr Digital,
Freyr SUBMIT PRO
Revamp Your FDA Compliance Game with a Submission Software: Here's How!
2 min read
April 7, 2023
Freyr Digital,
Freyr SUBMIT PRO
Mastering eCTD Submissions: Best Practices for Streamlined Regulatory Approval
1 min read
March 16, 2023
Freyr Digital,
Freyr SUBMIT PRO
eCTD: The Future of Regulatory Submissions - Leaving NeeS in the Past
1 min read
February 23, 2023
Freyr Digital,
Freyr SUBMIT PRO
Submission Excellence: Get New Products to Market Faster
2 min read
February 17, 2023
Freyr Digital,
Freyr SUBMIT PRO
Paperless Regulatory Submissions in China - A Big Market Opportunity
3 min read
February 6, 2023
Freyr Digital,
Freyr SUBMIT PRO
How to Choose the Right eCTD Submissions Vendor: A Comprehensive Guide
2 min read
January 13, 2023
Freyr Digital,
Freyr Submit Track
eCTD Submissions Planning & Tracking: A Key to Successful Submissions
2 min read
January 4, 2023
Freyr Digital,
Freyr SUBMIT PRO
Automation: A Helping Hand While Transitioning to eCTD 4.0
5 min read
December 23, 2022
Freyr Digital,
Freyr SUBMIT PRO
eCTD and CTD Filing Procedures for the US and Canada – Challenges & How to Avoid Them?
3 min read
November 29, 2022
Freyr Digital,
Freyr SUBMIT PRO
Getting Ready for Adoption of eCTD 4.0