This practical session showcases a clear and realistic approach for evaluating and implementing AI solutions in the pharma/device regulatory space.
You’ll learn how to set expectations with both end users and leadership, identify and prioritize the right internal use cases, and apply objective criteria to assess vendors and applications.
We’ll also highlight how AI is being put to work in Regulatory today, including examples such as responding to Health Authority questions (e.g., RTQs) and managing Health Authority letters and correspondence, along with a look at what’s coming next.
