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Current Regulatory Landscape Impacting Medical and Scientific Communications
Program Code:
388
Date:
Wednesday, June 26, 2013
Time:
4:00 PM to 5:30 PM
EST
CHAIR
:
Mary K Sendi,
PharmD (SCHNON), Director and Team Lead, Medical Information,
Pfizer Inc, United States
Mary is Regional Therapy Area Lead in Medical Information accountable for implementing MI global®ional strategies related to product support for Pfizer’s Immunology Inflammation Therapy Areas. Mary is responsible for MI Immunology Inflammation therapy area operations for Canada and US.
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SPEAKER
(S):
Jeff Francer is Assistant General Counsel of the Pharmaceutical Research and Manufacturers of America (PhRMA), where he provides advice and advocacy to the Association and its member companies on FDA regulatory and policy matters.
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Melissa L. Harris, PharmD (SPKNON), Executive Director, US Medical Information and Field Medical Operations, Bristol-Myers Squibb Company, United States
Stuart Sowder,
JD,PharmD,MBA (SPKNON), Vice President, External Medical Communications,
Pfizer Inc, United States
Stuart Sowder leads Pfizers Global External Medical Communications group. His work includes leadership for Medical Information, Field Based Medical, Publications, Investigator Initiatied Research, Medical Education, and all of Pfizer's Transparency initiatives.
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Description
This session will address how FDA regulatory guidance documents affect the pharmaceutical industry, impacting how externally-facing medical functions communicate medical and scientific information to health care professionals and consumers.
This session has been developed by the Medical Communications Community.