Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Automate core regulatory report documents across the CTD pyramid and dramatically accelerate submission timelines.
Event
📅 June 14–18, 2026 in Philadelphia, PA
📍 Pennsylvania Convention Center
Join Yseop at the DIA 2026 Global Annual Meeting, where regulatory, clinical, and technology leaders come together to shape the future of life sciences.
Meet with our team to discover how Yseop is helping organizations move beyond basic content generation toward regulatory grade AI that delivers scalable, compliant, and submission ready outputs across document workflows.
📅 Tuesday, June 16 | 12:25 PM – 12:55 PM
📍 Innovation Theater 1
👤 Presented by Jenni Pickett, PhD and Camille Sauder, Yseop
Content generation is easy. Delivering outputs that are accurate, traceable, and consistent enough for regulatory submission across diverse document types is not.
As teams expand beyond CSR automation into protocol, CMC, and pharmacovigilance workflows, many AI solutions struggle to adapt, creating challenges around compliance, scalability, and usability.
In this session, Yseop will explore what regulatory grade AI looks like in practice. Through real workflow examples, attendees will see how configurable, agentic systems embed compliance and validation behind the scenes while adapting to specific business needs, enabling scalable, submission ready outputs without compromising control.
Let’s start automating your data to narratives today!