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Boston Convention and Exhibition Center

2013年6月23日 (日) 午前 8:30 - 2013年6月27日 (木) 午後 12:45

415 Summer Street, , Boston, MA 02210 , USA

DIA 2013 49th Annual Meeting: Advancing Therapeutic Innovation and Regulatory Science

Current Developments in the Automated NDA Field Alert Reporting Project

Session Chair(s)

Mark W. Browning, JD

Mark W. Browning, JD

Consumer Safety Officer, OMPQ, Office of Compliance, CDER

FDA, United States

This session will discuss the phase 1 pilot for development of an automated form used to submit data from the manufacturer to the Office of Regulatory Affairs and Office of Manufacturing and Product Quality.

Learning Objective : Discuss the new Automated NDA Field Alert initiative of the Office of Regulatory Affairs, Drug Surveillance and Reporting and Risk Science Intelligence and Prioritization teams within the Office of Manufacturing and Product Quality.

Speaker(s)

Karen E. D'Orazio

New ORA/CDER Field Alert Reporting Initiative

Karen E. D'Orazio

FDA, United States

Pre-Approval Manager, Office of Regulatory Affairs

Hitesh A. Patel

Electronic NDA Field Alert Reports: Industry Perspective

Hitesh A. Patel

United States

Mark W. Browning, JD

New ORA/CDER Field Alert Reporting Initiative

Mark W. Browning, JD

FDA, United States

Consumer Safety Officer, OMPQ, Office of Compliance, CDER

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