Managing Informed Consent Samples from Clinical Trials

A set of best practices for the definition, tracking and management of allowable use attributes associated with samples collected in protocol based clinical trials

Sample-level consent management is a critical component of clinical trials, especially follow-on and translational research. Best practice recommendations suggest that sponsors should  use a configurable system to define a flexible and manageable  set of attributes at the study, country, and site levels that can be applied to all samples collected over the duration of the trial. 

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