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Seaport Hotel

Aug 12, 2019 7:45 AM - Aug 14, 2019 4:00 PM

One Seaport Lane, Boston, MA 02210

Drug Safety and Pharmacovigilance Across the Product Lifecycle

Build a solid foundation in the key concepts of drug safety and pharmacovigilance throughout the medical product development lifecycle. Learn how to comply with regulatory requirements.

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Session 7: Clinical Trial Safety Regulations – EU Clinical Trial Safety Reporting

Session Chair(s)

Jill W. Buckley, PharmD

Jill W. Buckley, PharmD

Adjunct Assistant Professor

Rutgers, the State University of New Jersey, United States

This session will cover the safety reporting requirements in the EU for clinical trials as well as selected other countries.

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