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Mercure Amsterdam City Hotel

2024年5月29日 (水) 午前 8:00 - 2024年5月30日 (木) 午後 4:30

Joan Muyskenweg 10, 1096 CJ Amsterdam, Netherlands

Pharmacovigilance Strategies Workshop

Collaborate and Innovate for Patient-Centric Safety.

Session 5: RWE And Data Insights

Session Chair(s)

Esther  De Vries, MS, MSc

Esther De Vries, MS, MSc

Assessor Pharmacovigilance

MEB, Netherlands

James  Whitehead, MBA, MSc

James Whitehead, MBA, MSc

Former Senior Director Device & Digital Safety - AstraZeneca

Visiting Lecturer - Pharmacovigilance MSc Course, University of Hertfordshire, United Kingdom

The sources that inform pharmacovigilance actions continues to expand. One broad source is Real-World Data (RWD), which is data relating to patient health status and/or the delivery of health care routinely collected from a variety of sources. It becomes Real-World Evidence (RWE) when analysed and utilised as clinical evidence about a medical product's usage and potential benefits or risks. RWE compliments the data collected from other sources like clinical studies to enable the generation of a more holistic picture. To quote the EMA, “In pharmacovigilance, it has become mainstay to use routinely collected data about a patient’s health status or the delivery of healthcare from a variety of sources other than traditional clinical trials to support decision-making”

This session will focus on the insight that pharmacovigilance can derive from the growing sources of data before diving into case studies on the utilisation of RWD and RWE.

Speaker(s)

Andrej  Segec, MPharm, MS

DARWIN Project - Data Analysis and Real World Interrogation Network

Andrej Segec, MPharm, MS

European Medicines Agency, Netherlands

Scientific Administrator

Lutz  Nährlich

Registry Holder

Lutz Nährlich

Justus-Liebig-University Giessen, Germany

Departement of Pediatrics

Mark  Perrott, PhD

With additional participation of:

Mark Perrott, PhD

Axian Consulting Ltd., United Kingdom

Managing Partner

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