ClinicalTrialsgov Part 2 Definitions Laws and Regulations

>> YOUR LINK HERE: ___ http://youtube.com/watch?v=FiU89KN86nk

Part two of a three-part webinar series, FDA provides a general overview of relevant definitions, laws, and regulations for complying with ClinicalTrials.gov registration and results information submission requirements. • Speakers: • Jan Hewett, J.D. • Regulatory Counsel • Policy Office (PO) • Office of Scientific Investigations (OSI) • Office of Compliance (OC) • Center for Drug Evaluation and Research (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 2022 Playlist - • 2022 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

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