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Session Chair(s)
Jeffrey N. Stuart, PHD
Associate Vice President, Global Regulatory Affairs
Merck Sharp & Dohme LLC , United States
Learning Objective : Describe innovative co-development policies emerging for the most promising precision medicines; Analyze policy alternatives that enhance proper use of precision medicine and companion diagnostic combinations.
Speaker(s)
Navigating the Regulatory Pathway for Drug/Companion Diagnostic Co-Development in Precision Medicine
Kenneth G. Butz, MS
PPD, United States
Director, Regulatory Affairs
FDA Perspective
Christopher Leptak, MD, PHD
Greenleaf Health, Inc., United States
Executive Vice President, Drug and Biological Products
Opportunities and Barriers to Clinical Implimentation of Genomics in Oncology
Eric Padron, MD
H. Lee Moffitt Cancer Center and Research Institute, United States
Assistant Member, Section Head, Genomics and Personalized Medicine
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