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Virtual Event

2021 年 06 月 27 日 10:00 上午 - 2021 年 07 月 01 日 4:30 下午

Horsham, PA 19044

DIA 2021 Global Annual Meeting

Role of Clinical Pharmacology Guidances and Policies in Enhancing Drug Development

Session Chair(s)

Anuradha  Ramamoorthy, PHARMD, PHD

Anuradha Ramamoorthy, PHARMD, PHD

Policy Lead, OCP, OTS, CDER

FDA, United States

Clinical pharmacology informs dose selection, dose optimization, and therapeutic individualization. Effective clinical pharmacology guidances and policies support an efficient drug development process and consistent regulatory evaluation.

Learning Objective : Describe the value of clinical pharmacology guidances and policies in drug development;Recognize the lifecycle approach supporting the development and implementation of clinical pharmacology guidances; Discuss the role of regulatory research and other stakeholder input in the development of clinical pharmacology guidances and policies.

Speaker(s)

Rajanikanth  Madabushi, PHD

Role of Guidance and Policy in Advancing Clinical Pharmacology

Rajanikanth Madabushi, PHD

FDA, United States

Associated Director for Guidance and Scientific Policy, OCP, OTS, CDER

Samantha  Roberts, PHD

Advancing Clinical Pharmacology Through Regulatory Policy and Partnership

Samantha Roberts, PHD

AstraZeneca, United States

Senior Director, Regulatory Intelligence

Kathleen M. Giacomini, PHD

Academia Update

Kathleen M. Giacomini, PHD

University of California San Francisco, United States

Dean, School of Pharmacy, Professor and Principal Investigator

David  Boulton, PHD

Panelist

David Boulton, PHD

AstraZeneca, United States

Clinical Pharmacology and Quantitative Pharmacology Head of Post Marketing

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