Innovation to Impact: Drug Development, AI, and Regulatory Strategy
Click here to watch a video of this episode. [https://www.youtube.com/watch?v=N9nwB4TY-sw] In drug development, go/no-go decisions concentrate translational risk and expose real consequences. When AI or digital biomarkers influence that call, decision-grade evidence in a regulated environment is not optional. This episode sits in the moment every executive recognizes: the slide is on the screen and someone asks, “Do we advance?” Here’s the tension. We love the word validated, but what happens when the next dataset disagrees? We introduce a practical discipline we call the decision warranty: clear scope, clear evidence chain, clear boundaries, and explicit triggers for pause, rerun, or escalation. Someone has to own that call. Takeaway: if you cannot write the stop triggers and the decision owner on one page, do not let the tool move the decision. * (00:00) - Forward Looking Themes for 2025 * (01:00) - Reproducibility Crisis and Foundational Biology * (02:00) - Digital Measures and Preventive Health * (03:00) - Multimodal AI and Foundation Models * (06:00) - Closed Loop Data Generation and Innovation * (09:00) - Decision Making as a Core Capability * (13:00) - Human in the Loop and Accountability * (16:00) - Micro Physiological Endpoints and Decision Use Limits * (21:00) - Democratizing Data and Model Access * (24:00) - Biology as Foundation for Modeling Systems * (28:00) - Opportunity, Effort, and Due Diligence If you liked this episode, steal the monthly cheat sheet at Innovation2Impact Newsletter [https://innovationimpact.beehiiv.com/](we do the digging, you keep the credit).
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