Proven Gen-AI Innovation for Safety Narratives and ICFs
About this webinar
Regulatory medical writers face increasing pressure to deliver high-quality safety narratives and informed consent forms (ICFs) faster, without compromising accuracy, consistency or regulatory expectations. Traditional authoring workflows remain highly manual, repetitive and time-intensive.
This webinar introduces a new generation of Gen-AI-enabled authoring technology purpose-built to accelerate the creation of clinical trial safety narratives and ICFs. Attendees will see how Gen-AI can move beyond generic drafting assistance to support rapid, structured and compliant narrative generation, while preserving writer control and auditability.
Through real-world examples, the featured speaker will show how this innovation significantly reduces turnaround times by automating data interpretation, standardizing narrative logic and eliminating redundant manual steps, allowing writers to focus on medical judgment and quality review rather than first-draft assembly.
Register for this webinar to learn how Gen AI supports safety narratives and ICFs with speed, control and compliance-aligned workflows.
Who should attend
- Pharma and CRO’s
- Regulatory Medical Writers/leadership
- Clinical Operation Leadership
- Trial transparency
- Clinical Trial Innovation
What you will learn
- How specific, secure, closed-loop Gen-AI can effectively accelerate safety narrative and ICF authoring
- Where speed gains are achieved without sacrificing regulatory rigor
- Why secure, closed-loop gen-AI is a must for regulatory writing
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
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.
