| 2006D-0331 | Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors; Exception from Informed Consent Requirements for Emergency Research | |||||||||||||||||||||||
| FDA Comment Number : | EC10 | |||||||||||||||||||||||
| Submitter : | Ms. Elaine Daly | Date & Time: | 09/11/2006 10:09:13 | |||||||||||||||||||||
| Organization : | Ms. Elaine Daly | |||||||||||||||||||||||
| Category : | Individual Consumer | |||||||||||||||||||||||
| Issue Areas/Comments | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| It is inhumane to experiment on anyone without their consent. There should be something that would cover this added to the organ doaner card. | ||||||||||||||||||||||||