Re-consent

In Running the trial

Re-consent is obtaining a participant's agreement again after important new information appears or the trial changes in a way that could affect their willingness to continue. Typical triggers are a new safety finding, a substantial protocol amendment, or a longer follow-up period. It uses the newly approved version of the consent form.

Turn the vocabulary into a career

The free CRLN Career Finder maps your background to a clinical-research role and builds a step-by-step roadmap. No cost, no card.

Educational reference only. Where regional rules differ, follow the regulation and the written procedures that apply where you work.