Webinar: The CTD to eCTD Transition Playbook: Formatting Source Documents for Regulatory Success
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Transitioning from CTD to eCTD is a major milestone for any region. The secret to a seamless shift doesn't lie in the final publishing software. It starts long before that, right inside your source documents.
If you are operating in a region that is currently planning, piloting, or navigating the transition to eCTD, this webinar is your blueprint.
Whether you are a health authority shaping new submission guidelines or an industry professional preparing your pipeline for upcoming mandates, the key to success is early document readiness. We have seen too many times how poor formatting leads to costly delays, frustrating rework, and technical rejections. That is why we invite you to our complimentary session, where you receive a free “playbook” that serves as your guide to a successful eCTD submission!
Join us to discover how to future-proof your authoring habits today to position you perfectly for the regulatory requirements of tomorrow. We will break down the technical rules, bust common myths, and show you exactly how to make your documents "eCTD-ready" from day one.
Date: 07 October 2026
Time: 16:00 - 17:00 CEST
Participation is free of charge. Every participant receives a Certificate of Attendance.
Not sure if you can make it live? Register now to receive the recording!
Agenda Highlights:
- The Transition Landscape: Setting the stage for a collaborative shift between industry and regulatory agencies.
- Mythbusting & Technical Traps: A strategic look at the most common formatting pitfalls—from granularity to navigation—and how to avoid them.
- The ROI of Document Readiness: Why proactive formatting is your strongest asset to accelerate approvals and reduce agency queries.
- Mastering the Authoring Lifecycle: Translating rigid technical eCTD rules into sustainable, everyday authoring habits.
This session is exclusively designed for stakeholders in regions where eCTD is on the horizon or in the early stages of implementation:
- Health Authorities & Regulators looking to understand industry challenges and define smooth transitional processes.
- Regulatory Affairs & Submission Teams preparing their dossiers for upcoming regional eCTD mandates.
- Medical & Regulatory Writers who want to master eCTD-compliant formatting standards.
- Local Affiliates adapting global documents for transitioning markets.
Don’t wait until eCTD is fully mandated to change your authoring habits. Master the transition now and set your teams up for regulatory success!
Your Speakers:
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Sylvie Colin Senior Business Consultant and Publishing Services Lead |
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Frank Dickert |