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Last Updated: October 3, 2026
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CDER's Deputy Center Director for Clinical Science Robert J. Temple, M.D., shares case studies and FDA perspectives on why ... Cynthia F. Kleppinger from CDER's Office of Scientific Investigations describes what a Jean Mulinde from CDER's Office of Scientific Investigations describes the casic characteristics of clinical trials of Short video interview series episode 5 of 14 CDER's Director of the Division of Generic Drug Bioequivalence Evaluation Seongeun (Julia) Cho discusses bioequivalence ... CDER's Director of Division of Clinical Compliance Evaluation Ni A. Khin, M.D. defines good clinical practice ( These presentations examined the global status of clinical trials and new trial designs, focusing on sponsor oversight ... Discover the importance of Source Kassa Ayalew from CDER's Division of Clinical Compliance Evaluation (DCCE) discusses medical product approval and ...
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