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Last Updated: October 3, 2026
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Jean Mulinde from CDER's Office of Scientific Investigations describes the casic characteristics of clinical trials of Cynthia F. Kleppinger from CDER's Office of Scientific Investigations describes what a CDER's Deputy Center Director for Clinical Science Robert J. Temple, M.D., shares case studies and FDA perspectives on why ... This webinar is of special interest for clinical trial Welcome to this lecture on Clinical Trial Execution and Good Clinical Practice, part of the comprehensive course Clinical Trials ... The premise behind RBQM is that monitoring In this video you will learn concepts on CDER's Director of Division of Clinical Compliance Evaluation Ni A. Khin, M.D. defines good clinical practice ( Welcome to this educational lecture on The new ICH E6(R3) is here, bringing significant changes to clinical trial conduct. For Clinical The FDA, EMA, and ICH Guidance has suggested more emphasis on centralized oversight of trials and less on onsite visits. Air date: Sunday, January 30, 2022, 12PM
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