Accelerate Regulatory Writing with Gen-AI Without Prompt Engineering
About this webinar
Generative AI (Gen-AI) is rapidly changing the way regulatory documents are created, but adopting AI into the regulatory writing process can introduce a new challenge: prompt engineering. Instead of spending time developing and refining prompts, learning how to communicate with AI and troubleshooting inconsistent outputs, regulatory medical writers can focus on applying scientific expertise, shaping the message and exercising critical judgment for conclusions.
This webinar will explore an approach to Gen-AI for regulatory writing, designed to bring Gen-AI directly into the medical writer’s existing workflow without requiring writers to divert critical time to become prompt engineers. Attendees will see how to generate regulatory content based on the underlying relationships between source content and the document being created, helping accelerate the regulatory writing process from a prompt-driven activity to a faster, more intuitive and content-driven workflow. A key component of this approach is content-based mapping, which leverage relationships between source materials and regulatory documents to support appropriate content reuse.
The featured speaker will also demonstrate how this approach works directly within Microsoft Word, allowing writers to leverage AI capabilities within a familiar authoring and review experience. This integration is designed to minimize workflow disruption while supporting greater efficiency, consistency and reuse.
Whether an organization is “experimenting” with Gen-AI or still evaluating how AI can fit into the regulatory writing process, this webinar will demonstrate what becomes possible when a Gen-AI works around the writer’s workflow, not the writer around the AI.
Register for this webinar to learn how regulatory writing can use Gen-AI to reduce prompt engineering, accelerate document development and keep writers in control of scientific judgment and content review.
Who should attend
- Regulatory Medical Writers
- Any level – Medical Writer
- Clinical Operations leadership
- Clinical Trial Digital Transformation professionals
- Clinical Trial Innovation professionals
- Regulatory Strategy professionals
What you will learn
- Generate regulatory content without requiring writers to engineer complex prompts
- Connect source content to regulatory documents through content-based mapping
- Work directly within Microsoft Word
- Reduce CSR first-draft times by 70%
- Create consistency and accelerating regulatory submissions
- Keep regulatory medical writers at the center of scientific judgment and content review while reducing manual document creation
Featured Speakers
Mark Pittman
Mark’s career began in software development, where he spent more than a decade building solutions for some of the world’s largest companies. That experience provided him with both a deep technical foundation and a front-row seat to witnessing how innovation can transform industries. His full immersion into life science technology came with the chance to apply AI and machine learning to one of the most critical areas of clinical research: Regulatory Writing.
For Mark, this was more than just a career shift; it was an opportunity to make a meaningful impact. He brings an empathetic perspective to the thousands of medical writers who have spent years creating regulatory documents through painstaking manual effort. Mark thrives on listening to their challenges, exploring what slows them down and demonstrating how closed-loop GenAI tools, like ZYLIQ, can change their day-to-day work.
Partner for this event
ZyliQ.AI
ZYLIQ is an industry leading platform for leveraging Gen-AI for Regulatory Writing. Emerging from 30 years of CRO experience and software development, ZYLIQ is the perfect blend of both creating software for CSRs, PLSs, Narratives and more. ZYLIQ’s unique blend of Gen-AI and AI libraries has created the most effective tools, helping writers save 70% of their creation time.