Tyler is the Senior Director of Regulatory Affairs at Pfizer, where he leads U. S. FDA strategy for late-stage and marketed pharmaceuticals. With a Master of Science from Columbia University, he specializes in NDA submissions and post-market lifecycle management, focusing on mitigating risk and ensuring regulatory clarity for complex therapies.
He has a keen interest in how the Regulatory Affairs function is evolving from a downstream role to being central to innovation in the pharmaceutical industry.
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