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Content in this video provided updates and cutting-edge insight on novel artificial intelligence (AI), clinical trial designs and innovative strategies, safety data in clinical trials, combination products, electronic submissions and more. Subject matter experts provided insight on FDA’s perspectives, adoption of regulatory guidelines, opportunities for stakeholders to engage with CDER and best practices. Timestamps 01:55 – Selective Safety Data Collection in Clinical Trials 29:59 – Q&A Session 44:45 – Enhancing Clinical Trial Innovation 01:10:29 – Q&A Session Speakers: Mary T. Thanh Hai, MD Deputy Director for Clinical Office of New Drugs (OND) Center for Drug Evaluation and Research (CDER) | FDA Kevin Bugin, PhD, MS, RAC Deputy Director OND | CDER | FDA Learn more at: https://www.fda.gov/drugs/news-events... ----------------------- FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in understanding the regulatory aspects of human drug products & clinical research. Upcoming Training - https://www.fda.gov/cdersbia SBIA Listserv - https://public.govdelivery.com/accoun... SBIA 2024 Playlist - • 2024 CDER Small Business and Industry... SBIA LinkedIn - / cder-small-business-and-industry-assistance SBIA Training Resources - https://www.fda.gov/cdersbialearn Twitter - / fda_drug_info Email - [email protected] Phone - (301) 796-6707 I (866) 405-5367