Principal Consultant and President
CP Pathways LLC
Doug Mead is Principal Consultant at CP Pathways LLC, focused on regulatory submissions and strategy related to combination product submissions. Previously, he was Senior Director, Global Regulatory Affairs, Medical Devices and Combination Products, for Janssen Research & Development LLC, and, for 13 years, was responsible for establishing and implementing the worldwide regulatory strategy for the development of drug delivery systems and drug-device combination products. These included a variety of injector and infusion systems, microcatheters, and nasal spray devices. Before joining Janssen, he held positions at a regulatory law firm, a pharmaceutical company specializing in drug delivery, various surgical instrument companies, and a medical device testing laboratory. He has an M.S. Degree in Biomedical Engineering from Drexel University and over 35 years of experience in the medical device, pharmaceutical, and combination products industries.
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Drug-Led Combination Products - Submission Guidance and Contents
Wednesday, October 4, 2023
8:00 AM – 9:15 AM EDT