Jun 30
Why Re-Consent Is Essential in Clinical Trials
Clinical trials don't remain static. As studies progress, new findings or protocol updates may require participants to review fresh information before deciding whether to continue. This process, known as re-consent, helps protect participant rights while promoting transparency and ethical research practices. It ensures everyone stays informed about changes that may affect their participation. If you'd like to understand how re-consent supports safer and more responsible clinical research, DecenTrialz offers a comprehensive guide that explains the process in detail.
