| 2006D-0331 | Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors; Exception from Informed Consent Requirements for Emergency Research | |||||||||||||||||||||||
| FDA Comment Number : | EC1 | |||||||||||||||||||||||
| Submitter : | Mr. Darryl Wellinghoff | Date & Time: | 09/05/2006 11:09:22 | |||||||||||||||||||||
| Organization : | Mr. Darryl Wellinghoff | |||||||||||||||||||||||
| Category : | Individual Consumer | |||||||||||||||||||||||
| Issue Areas/Comments | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| This is important research and I personally would be more than willing to participate given a life threatening emergency. However, I am sure some special interest groups will push back. If there is push back, this could be handled in the same way that organ donation is handled. Have "emergency research" participation as an option to every person with a drivers license or state issued identification card. | ||||||||||||||||||||||||