R esearch in emergency care has been facilitated by an exception from the requirements for obtaining and documenting informed consent. This exception only applies to a strictly limited class of research, involving activities that may be carried out in human subjects who are in need of emergency therapy and for whom, because of the participants' medical condition, and the unavailability of legally authorized representatives of the subjects, no legally effective informed consent can be obtained. 1 These regulations (21 CFR 50.24 for Food and Drug Administration [FDA] regulated studies and/or a Secretarial Waiver in 45 CFR Part 46 for the Department of Health and Human Services sponsored, funded or conducted studies) were introduced in 1996, and have allowed many key clinical trialswhich would otherwise not have been possible-to proceed and to positively transform emergency care in the process. This article explores the issue of how representative community consultation (CC), a requirement for such studies, can and should be, with particular reference to the use of interactive mediabased activities. While focused on trauma trials, the issues addressed are equally applicable to other emergent conditions associated with loss of capacity, such as cardiac arrest, stroke, or status epilepticus. 2