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

4 min read
March 7, 2025
Freyr Digital,
Freyr SUBMIT PRO
EMA’s Roadmap for eCTD 4.0 - Key Updates and Insights
4 min read
February 19, 2025
Freyr Digital,
Freyr SUBMIT PRO
The AI Advantage in Health Authority Queries Management
3 min read
February 6, 2025
Freyr Digital,
Freyr SUBMIT PRO
The Future of Regulatory Submissions: Trends to Watch in 2025
3 min read
January 31, 2025
Freyr Digital,
Freyr SUBMIT PRO
Best Practices for Implementing an eCTD Submission Software
4 min read
January 23, 2025
Freyr Digital,
Freyr rDMS
Mitigating Regulatory Risk with a Robust Document Management System
5 min read
January 16, 2025
Freyr Digital,
Freyr SUBMIT PRO
USFDA's eCTD 4.0 Update: Key Takeaways
2 min read
January 10, 2025
Freyr Digital,
Freyr SPAR
The Future of RIMS Software: Trends and Innovations
3 min read
January 8, 2025
Freyr Digital
Understanding USFDA Form 483: Everything You Need to Know
6 min read
December 23, 2024
Freyr Digital
Generative UI: Revolutionizing User Interfaces with Real-Time Adaptability
3 min read
December 20, 2024
Freyr Digital
Are You Prepared for the Next Regulatory Audit?
3 min read
December 10, 2024
Freyr Digital,
Freyr SUBMIT PRO
The Strategic Advantage of Partnering with the Right eCTD Solution
2 min read
December 6, 2024
Freyr Digital,
Freyr rDMS
Mastering Global Regulatory Document Management: Challenges, Solutions, and Transformative Strategies