Sponsored session: Zyliq Effective Ways to Evaluate AI Tools for Regulatory Writing

Description

As AI tools proliferate in medical writing, organisations face critical decisions about which solutions to trust with their regulatory documentation. This practical seminar cuts through the hype to provide frameworks and scorecards for evaluating AI tools, addressing key concerns around security, sustainability, and implementation timelines. Mark Pittman (CRO, Zyliq) and Martin will explore the build-versus-buy decision, share lessons from real-world implementations, and equip delegates with essential questions to ask any AI vendor. Participants will gain actionable tools for assessment, including a pilot scorecard framework, helping them make informed decisions that balance innovation with compliance in their medical writing operations.​​​​​​​​​​​​​​​​