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Walter E. Washington Convention Center

2015 年 06 月 14 日 2:30 下午 - 2015 年 06 月 18 日 6:45 下午

801 Mount Vernon Place, NW, , Washington, DC 20001-3614 , USA

DIA 2015 51st Annual Meeting: Develop. Innovate. Advance.

Full conference and one-day registrants will have access to presentation PDFs through Friday, December 18, 2015 <A href="http://www.diaglobal.org/Flagship-Meetings/DIA-Annual-Meeting/Meeting-Program/ePac-Presentations-Access.aspx">Review Presentations </A>

Social Media: Opportunities and Challenges in Pharmacovigilance and Clinical Research

Session Chair(s)

Martin  Harvey Allchurch, LLM

Martin Harvey Allchurch, LLM

Head of International Affairs

European Medicines Agency, Netherlands

This session will discuss the potential of social media as a new data source in the early detection of safety issues related to medicines. Social media usage has increased substantially within the last five years, including the creation, sharing or exchange of information on health-related topics and has already shown promise in the management of disease outbreaks, for example. Therefore, the expectation is that the use of data from a real-world, large-scale population of consumers and patients will result in more comprehensive and timely information about the safe use of medicines. However, this new data source also brings a number of challenges such as compliance with data privacy requirements, ethical aspects or risks in compromising clinical research results, which will be further outlined. Lessons learned from MedWatcher Social as well as the approach towards social media analytics currently being researched in the context of the Innovative Medicines Initiative (IMI) WEB-Recognising Adverse Drug Reactions (RADR) project will be discussed.

Learning Objective : Discuss social media analytics for the purpose of detecting new safety issues and medical insights in relation to medicines based on MedWatcher Social platform; Describe the impact of the use of social media by clinical study participants on clinical research; Discuss the WEB-Recognising Adverse Drug Reactions (RADR) project; Describe data privacy implications and ethical and societal aspects in relation to the use of social media analytics for the purpose of pharmacovigilance.

Speaker(s)

Alexis Reisin Miller, JD

Social Media: Impact on Clinical Studies

Alexis Reisin Miller, JD

Merck & Co., Inc., United States

Head, Global Regulatory Policy

Carrie E. Pierce, MBA, MPH

Digital Drug Safety

Carrie E. Pierce, MBA, MPH

Epidemico, United States

Senior Project Manager

Martin  Harvey Allchurch, LLM

Social Media Analytics

Martin Harvey Allchurch, LLM

European Medicines Agency, Netherlands

Head of International Affairs

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