Webinars
DCL Learning Series
Upcoming Webinars
The DCL Learning Series covers topics that relate to content and data conversion with an instructional twist. DCL speaks with industry experts and brings meaningful presentations and conversation direct to your screen. Topics include research integrity, DITA, S1000D, Section 508 and accessibility, XML standards, PubMed, artificial intelligence, and much more.
Our webinar calendar is constantly updated. Click the link to receive alerts for upcoming webinars.
KEYWORDS:
pharmaceutical, pharma, dossier development, FDA submissions, regulatory compliance, artificial intelligence, content management, automated content generation, common technical document, Data Conversion Laboratory, Content Rules, Inc.
SPEAKERS:
David Turner, Consultant and Head of Partner Relations, Data Conversion Laboratory
Regina Lynn Preciado, Senior Director of Content Strategy, Content Rules
Modernizing Pharma Dossier Development with AI and Structure
Wed, Apr 23, 2025 12:00 PM - 1:00 PM EDT
Accuracy, Efficiency, and Compliance from Source to Submission
Innovative pharma companies are proving that AI solutions can accelerate dossier development and submission management - while preserving quality and accuracy. The keys to their success?
1. Consistent, accurate source content enabling excellent AI-generated derivatives
2. Optimized workflows ensuring data integrity, regulatory compliance, and operational efficiency
3. Intuitive content ecosystems empowering AI assistants and content automation
Dive deeply into the content management ecosystem of the future in this fun and interactive webinar to see how authoring practices shape the results of AI solutions implemented throughout your company. Learn where to focus efforts on automated content generation throughout the common technical document (CTD). Discover how a new way of working, enabled by technology, helps your team achieve its number one goal: to get safe, effective medicines to patients sooner.
If you’re a pharma professional managing complex documentation, register for this session to equip yourself with knowledge and tools to modernize regulatory processes, streamline operations, and stay ahead in a rapidly evolving digital landscape.
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