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We have written a free eCTD Validaiton and Viewer software for the entire world.
-This software allows you to view and validate eCTDs for almost all major territories of the world.
- The compiler is paid. Please contact us if you want to buy it.
Link to Free Viewer and Validator
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DISCOVER THE ATOMIC-ECTD ADVANTAGE
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Why settle for expensive, complex eCTD solutions when you can experience
professional-grade validation and viewing for FREE?
The Atomic-eCTD Viewer Lite gives you instant access to:
✓ Multi-Region Validation - Test your submissions against 11 regulatory
authorities (EU, US FDA, Canada, Japan, and more)
✓ Professional Reports - Generate validation reports in multiple formats
(TXT, CSV, HTML, PDF) that you can share with your team
✓ Interactive Viewer - Navigate your eCTD submissions with ease, track
document lifecycle, and preview PDFs instantly
✓ Zero Setup - No installation, no complexity. Just download and run.
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FROM VALIDATION TO COMPILATION: THE FULL ATOMIC-ECTD STORY
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The Lite Edition is Your First Step
Start with our FREE Lite edition to validate and view your eCTD submissions.
Experience the quality, accuracy, and ease-of-use that sets Atomic-eCTD apart.
When you're ready to create new sequences, upgrade to our FULL edition and unlock the complete eCTD lifecycle management solution.
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THE FULL EDITION: LOW-COST, HIGH-VALUE GLOBAL COMPILER
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Why Atomic-eCTD Full Edition is Your Best Investment:
1. AFFORDABLE PRICING
• Fraction of the cost of enterprise solutions
• No per-user licensing fees
• No annual subscription traps
• One-time purchase with lifetime updates
• Perfect for small to medium pharmaceutical companies
• Ideal for CROs and regulatory consultants
2. GLOBAL REACH
• Support for 11+ regulatory regions in ONE tool
• EU (EMA), US FDA, Health Canada, COFEPRIS (Mexico)
• SAHPRA (South Africa), SFDA (Saudi Arabia/GCC)
• TGA (Australia), FDA Thailand, JFDA (Jordan)
• ANVISA (Brazil), PMDA (Japan)
• No need to purchase separate tools for each region
• Consistent workflow across all territories
3. COMPLETE LIFECYCLE MANAGEMENT
• Create new sequences with intelligent wizards
• Validate against regional requirements
• View and navigate complex dossiers
• Track document lifecycle across sequences
• Export to multiple formats
• Database-driven for reliability and speed
4. FUTURE-PROOF TECHNOLOGY
• Built on modern, maintainable architecture
• Regular updates and improvements
• Active development roadmap
• Responsive support from developers
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THE eCTD V4 IMPERATIVE: BE READY FOR THE FUTURE
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The Regulatory Landscape is Changing - Are You Prepared?
eCTD v4 (Regulated Product Submission / RPS) is Coming:
• ALREADY MANDATORY in Japan (PMDA) since 2023
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