Skip to main content
I’m Curious-Show Me
×
Sign Up for a Live Demo
×
Talk to Us
×
Products
Toggle submenu
freya fusion Suite
AI-Enabled Regulatory Cloud
Freyr Digital Suite
Legacy Regulatory Software
Freya Fusion Menu Block
freya.intelligence
freya.register
freya.submit
freya.docs
freya.automate
freya.content
freya.RTQ
freya Chatbot
freya.label
Latest Blog
AI for global compliance: FDA, EMA, PMDA
Freyr Digital Menu Block
Freyr SUBMIT PRO
Freyr rDMS
Freyr SPL-SPM
Latest Blog
AI for global compliance: FDA, EMA, PMDA
freya fusion Suite
freya.intelligence
freya.register
freya.submit
freya.docs
freya.automate
freya.content
freya.RTQ
freya Chatbot
freya.label
Freyr Digital Suite
Freyr SUBMIT PRO
Freyr rDMS
Freyr SPL-SPM
Solutions
Toggle submenu
By Regulatory Functions
By Industry
Function Menu Block
Submission Management
Registration Management
Regulatory Intelligence
Document Management
Content Management
Labeling Management
Latest Blog
AI for global compliance: FDA, EMA, PMDA
Industries Menu Block
Medicinal Products
Medical Devices
Consumer
Global Regulatory Intelligence
Latest Blog
AI for global compliance: FDA, EMA, PMDA
Function
Submission Management
Registration Management
Regulatory Intelligence
Document Management
Content Management
Labeling Management
Industries
Medicinal Products
Medical Devices
Consumer
Global Regulatory Intelligence
Insights
Toggle submenu
Blogs
Brochures
Case Studies
Infographics
Success Stories
Webinars
What is ...?
White Papers
Podcasts
Company
Toggle submenu
About Us
Contact Us
Why freya fusion
Press Releases
Careers
Testimonials
PartnerUp
Trust Center
Compliance & Security
Book a Live Demo
Breadcrumb
Home
ECTD Submissions
eCTD Submissions
April 18, 2025
Key Updates on TGA’s eCTD 4.0 Rollout
April 11, 2025
Global Regulatory Harmonization Efforts in 2025
March 7, 2025
EMA’s Roadmap for eCTD 4.0 - Key Updates and Insights
February 6, 2025
The Future of Regulatory Submissions: Trends to Watch in 2025
January 31, 2025
Best Practices for Implementing an eCTD Submission Software
January 16, 2025
USFDA's eCTD 4.0 Update: Key Takeaways
December 10, 2024
The Strategic Advantage of Partnering with the Right eCTD Solution
March 16, 2023
eCTD: The Future of Regulatory Submissions - Leaving NeeS in the Past
February 17, 2023
Paperless Regulatory Submissions in China - A Big Market Opportunity
February 6, 2023
How to Choose the Right eCTD Submissions Vendor: A Comprehensive Guide
January 13, 2023
eCTD Submissions Planning & Tracking: A Key to Successful Submissions
November 29, 2022
Getting Ready for Adoption of eCTD 4.0
Pagination
View More