Home » Checklist Guides IRBs Through Informed Consent in CER Trials
Checklist Guides IRBs Through Informed Consent in CER Trials
October 24, 2013
Comparative-effectiveness research (CER) poses unique ethical dilemmas and potential risks not encountered in more traditional clinical studies, a group of leading bioethicists says. To help IRBs and investigators fully convey those risks to patients, they’ve prepared a checklist to follow when obtaining informed consent.