DIA 2012 Collaborate to Innovate
48th Annual Meeting
June 24-28, 2012
Philadelphia, PA
June 24-28, 2012
Philadelphia, PA
Pennsylvania Convention Center
What questions are on your mind regarding Social Media? Feel free to post a comment on your concerns or successes below.-W
Social media creates challenges and opportunities for the promotion and safety of drugs and other medical products. FDA and industry are working to optimize truthful product information and ways to gather adverse event data utilizing this resource
Tracks: Advertising & Promotion|Regulatory Affairs|Medical Communications
Presentation(s) & Speaker(s):
FDA Perspective
Thomas W. Abrams, MBA,RPh, Director, Office of Prescription Drug Promotion, CDER
FDA
Panelist
Gerald J. Dal Pan, MD, Acting Director, Office of Surveillance and Epidemiology, CDER
FDA
Industry Perspective
Paul James Savidge, JD,MBA, Vice President and Associate General Counsel
Bristol-Myers Squibb Company
Elizabeth E. Garrard, PharmD,RPh, Chief Safety Officer
Drug Safety Alliance, Inc.
FDA Perspective
Thomas W. Abrams, MBA,RPh, Director, Office of Prescription Drug Promotion, CDER
FDA
Panelist
Gerald J. Dal Pan, MD, Acting Director, Office of Surveillance and Epidemiology, CDER
FDA
Industry Perspective
Paul James Savidge, JD,MBA, Vice President and Associate General Counsel
Bristol-Myers Squibb Company
Elizabeth E. Garrard, PharmD,RPh, Chief Safety Officer
Drug Safety Alliance, Inc.
This session will focus on the specific types of social media currently being used by pharmaceutical companies with discussion on their successes and challenges. In addition, discussions on AE identification and collection while emphasizing the need for practices and guidance on the use of social media.
Tracks: Clinical Research|Medical Communications|Advertising & Promotion
Presentation(s) & Speaker(s):
Embracing and Incorporating New Technology (eg. Social media, iPad) into a Modern Pharmacovigilance System
Gregory J. Fiore, MD, President
SSI Strategy
Safety and Social Media: Returning the Intention to Report: Adding the Human Factor Back to High Tech
Michael A. Ibara, PharmD, Head of Safety Innovation
Pfizer Inc
Gregory J. Fiore, MD, President
SSI Strategy
Safety and Social Media: Returning the Intention to Report: Adding the Human Factor Back to High Tech
Michael A. Ibara, PharmD, Head of Safety Innovation
Pfizer Inc
Social media has huge potential as a new set of tools to drive patient recruitment. How do you use it and what happens when you do? In this symposium, we will offer both successes and lessons learned from trying social media as a recruitment strategy.
Tracks: Advertising & Promotion
Presentation(s) & Speaker(s):
Is Social Media the New Technology for Helping Patients Find Clinical Trials?
Richard Mayewski, Global Trial Optimization Specialist
Merck & Co., Inc.
Finding the “ePatient” for Your Clinical Trial
Rodney William Butt, MBA,MSc,MT, Principal Consultant, Clinical Operations
Hamilton Medical Consultants Group, Canada
When Social Media Undermines Clinical Trial Performance
Elizabeth A Moench, President and Chief Executive Officer
MediciGlobal
Richard Mayewski, Global Trial Optimization Specialist
Merck & Co., Inc.
Finding the “ePatient” for Your Clinical Trial
Rodney William Butt, MBA,MSc,MT, Principal Consultant, Clinical Operations
Hamilton Medical Consultants Group, Canada
When Social Media Undermines Clinical Trial Performance
Elizabeth A Moench, President and Chief Executive Officer
MediciGlobal
Title: Communicating Drug Safety Information Using Social Media: FDA and Industry Perspectives
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.
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.
Tracks: Medical Communications|Clinical Safety/Pharmacovigilance|Regulatory Affairs
Presentation(s) & Speaker(s):
Communicating Drug Safety Information: FDA Perspective
Catherine Yu Chew, PharmD, Acting Deputy Director, Division of Drug Information, CDER
FDA
Communicating Drug Safety Information :FDA Perspectives
Gregory Busse, PhD, Senior Writer/Editor, Team Lead for Drug Safety Communications, CDER
FDA
Communicating Drug Safety Information: Industry Perspective
Sue E. James, Vice President, Global Regulatory and Quality, Consumer Healthcare
GlaxoSmithKline
Catherine Yu Chew, PharmD, Acting Deputy Director, Division of Drug Information, CDER
FDA
Communicating Drug Safety Information :FDA Perspectives
Gregory Busse, PhD, Senior Writer/Editor, Team Lead for Drug Safety Communications, CDER
FDA
Communicating Drug Safety Information: Industry Perspective
Sue E. James, Vice President, Global Regulatory and Quality, Consumer Healthcare
GlaxoSmithKline
Title: Social Media 2.0: The Power of Online Rare Disease Communities to Connect and Engage ePatients
Relevant case studies will be presented to demonstrate how online patient communities and social media are revolutionizing how patients gain access to disease and treatment information.
Tracks: Advertising & Promotion|Clinical Research
Presentation(s) & Speaker(s):
RareConnect: A Global Social Network for Rare Disease Communities and Patients
Mary Dunkle, Vice President of Communications
National Organization For Rare Disorders (NORD)
The Power of Patient-driven Research and Rare Disease Online Communities: The SCAD Ladies and Beyond
Brian Loew, CEO
Inspire
Biopharma and Social Media: A Case Study
Eric Grinstead, Senior Vice President, Commercial Operations
Synageva Biopharma Corporation
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