What happens when a consent form changes and participants need to re-consent?

Clinical trials evolve. New information may become available, protocols may change, or an updated consent form may need to be reviewed and signed by participants. Whatever the reason, 5thPort supports re-consent and version control throughout the study.

Study teams can manage approved consent versions, issue the appropriate version to participants, and track which version each participant received and completed. This makes it easier to manage changes across participants and study sites while maintaining a clear, traceable record of what changed, which version was used, and when.