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Session Chair(s)
Maria Wishart
Medical Director, Global Patient Safety
Astrazeneca, United Kingdom
Learning Objective : Learn how mobility can facilitate ADR reporting. Learn how pharmaceutical companies can achieve live monitoring of ADRs related to their marketed products. Learn how pharmaceutical companies can achieve a closer interaction with patients regarding ADR reporting.
Speaker(s)
Adverse Drug Reaction (ADR) reporting via mobile devices
Maiken Hedegaard, MPHARM
NNIT A/S, Denmark
Life Science IT Consultant
Social Media and Pharmacovigilance: Socialvigilance
Nabarun Dasgupta, PHD, MPH
Epidemico, Inc. , United States
Chief Science Officer
Online patient reporting of adverse events: a case study
Monica Elisabet Plöen, RPH
CTC Clinical Trail Consultant AB, Sweden
Safety Officer & Medical Coder