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Communicating Drug Safety Information Using Social Media: FDA and Industry Perspectives
Program Code:
158
Date:
Monday, June 25, 2012
Time:
3:30 PM to 5:00 PM
EST
CHAIR
:
CDR Chew is Deputy Director of FDA’s Division of Drug Information and chair of the CDER Social Media team, administering the listserv and Twitter, and producing audio and video podcasts. She is also Director of FDA Regulatory Pharmaceutical Fellowship and a Commander in the US Public Health Service.
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PRESENTER
(S):
CDR Chew is Deputy Director of FDA’s Division of Drug Information and chair of the CDER Social Media team, administering the listserv and Twitter, and producing audio and video podcasts. She is also Director of FDA Regulatory Pharmaceutical Fellowship and a Commander in the US Public Health Service.
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Gregory Busse, FDA, United States
Sue James, GlaxoSmithKline, United States
Description
FDA relays the latest drug safety information through drug safety communications which are disseminated using social media tools. This session provides FDA and industry perspectives on the development, communication, dissemination, and impact of drug safety communications.
Learning Objectives:
Describe the development, dissemination, and impact of FDA Drug Safety Communications
Evaluate the reach and benefits of various social media tools
Differentiate between industry and FDA's reactions and efforts to communicate newly identified or potential drug risks to the public.