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DIA Global Center

Nov 04, 2019 8:15 AM - Nov 05, 2019 4:45 PM

21 Dupont Circle NW, Suite 300, Washington, DC 20036

Safety Risk Communication for Medical Products

Learn how to enhance the effectiveness of safety risk communication in light of evolving regulatory expectations by attending this course.

Session 9: Who’s Responsible for Communicating Drug Safety Information?

Session Chair(s)

Meredith  Smith, PhD, MPA, FISPE

Meredith Smith, PhD, MPA, FISPE

Senior Director, Implementation Science Pillar Lead

Evidera, Inc, United States

    This session will examine the role of regulatory authorities, pharmaceutical companies, and healthcare professionals in drug safety communication and will include an introduction to drug product labeling and drug advertising regulations in the US.

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