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European Medicines Agency

Nov 14, 2017 8:00 AM - Nov 14, 2017 4:45 PM

30 Churchill Place, Canary Wharf, London, E14 5EU, United Kingdom

EMA Information Day on Measuring the Impact of Pharmacovigilance Activities

How to measure pharmacovigilance activities to be effective and efficient? At this EMA Info Day you will learn about the revised PRAC strategy for measuring the effectiveness of the EU pharmacovigilance activities.

SESSION 3: METHODOLOGIES FOR IMPACT EVALUATION

Session Chair(s)

Bruce  Guthrie

Bruce Guthrie

NHS Research Scotland Primary Care Research Champion

University of Dundee, United Kingdom

Mona  Vestergaard Laursen, MPharm

Mona Vestergaard Laursen, MPharm

Senior Advisor, Data Analytics Centre

Danish Medicines Agency, Denmark

This session focuses on the validated methods for evaluating the impact of regulatory actions in terms of public health outcomes and what can we learn from case examples.

Speaker(s)

Christine  Hallgreen, DrSc, PhD

Methodological approaches to assessing risk minimisation interventions – study design, target population, data source, and outcome measures

Christine Hallgreen, DrSc, PhD

University of Copenhagen, Denmark

Associate Professor

Daniel  Morales, MD, PhD, MRCP

Time series regression as analytical approach – case examples

Daniel Morales, MD, PhD, MRCP

University of Dundee, United Kingdom

Member PRAC, Pharmacovigilance and Epidemiology Department

Nawab  Qizilbash, MD, PhD, MRCP, MSc

Outcome measures to evaluate the effectiveness of risk minimisation in EU PAS studies: A quantitative review

Nawab Qizilbash, MD, PhD, MRCP, MSc

OXON Epidemiology, Spain

Head

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