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Online

Mar 11, 2014 12:00 PM - Mar 13, 2014 2:00 PM

Development of a Clinical Study Report

Speakers

Diptee A. Gajjar, PhD

Diptee A. Gajjar, PhD

Intercontinental Regulatory Strategy Lead, Bristol-Myers Squibb Company, United States

Dr. Gajjar has over 20 years of research experience in pharmaceutical sciences; 16 years in pharmaceutical industry with expertise in scientific and regulatory writing. She began her career as a Clinical Pharmacologist for Janssen Pharmaceutica, a Johnson & Johnson affiliate. Thereafter, she joined the clinical pharmacology group at Bristol-Myers Squibb Co. and transitioned into medical writing. Since this time, she has led production of dossier for many regulatory submissions globally across multiple therapeutic areas.

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