Data monitoring committees (DMCs) play a critical role in ensuring the ethical conduct of clinical trials. Data monitoring committee charters set out the role and processes for data monitoring committees in monitoring clinical trials; however, little is known about the information that DMC charters contain. In this webinar, we will share results of an exploratory analysis of DMC charters, drawing out ethically and practically pertinent issues. These will be considered in light of findings from our broader project on ethical challenges faced by DMCs.
Presenters

Dr Lisa Eckstein is the CT:IQ Director and Ethics Specialist for Bellberry Ltd. She is an adjunct Senior Lecturer in the Faculty of Law at the University of Tasmania, where her research focuses on the regulation of clinical trials, genomic privacy, and consent.
Prof Seema Shah
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