Inaugural Group Meeting for Adverse Events in Clinical Trials. TMRP
Date: 10th May 15:00 - 17:00 BST
The Adverse Events in Clinical Trials Working Group is a sub-group of the TMRP Outcomes Working Group and we are having our inaugural meeting on 10th May 15:00 - 17:00 BST
If you are a researcher working in the area of adverse events (AEs) in clinical trials or have an interest in this field you may be interested to attend.
Objectives of the Adverse Events in Clinical Trials Working Group:
i. Motivate an interest for research on adverse events in RCTs
ii. Identify and bring together researchers interested in improving the collection, analysis, selection, and reporting of adverse events in RCTs.
iii. Identify research priorities for the assessment of adverse events in RCTs.
iv. Undertake new research activity for prioritised areas
In our first meeting we will be getting to know one another and we will be planning out a series of educational articles to help improve practice for the collection and analysis of adverse events.
We will also hear talks from:
Diana Papaioannou, Senior Research Fellow and Assistant Director at Sheffield Clinical Trials Research Unit, University of Sheffield
Kaspar Rufibach - Expert Statistical Scientist, Methods, Collaboration and Outreach Group, Roche Basel
If you are interested in joining and contributing to this working group please come along to our inaugural meeting to learn more. Please email Rachel Phillips [log in to unmask]<mailto:[log in to unmask]> for further details.
Rachel Phillips
Senior Lecturer in Medical Statistics
Pragmatic Clinical Trials Unit
Centre for Evaluation & Methods
Wolfson Institute of Population Health
Queen Mary University of London
Typical working pattern:
Monday/Wednesday/Thursday/Friday(am): Pragmatic Clinical Trials Unit, Queen Mary University of London
Tuesday/Friday(pm): Imperial Clinical Trials Unit, Imperial College London
You may leave the list at any time by sending the command
SIGNOFF allstat
to [log in to unmask], leaving the subject line blank.
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