| 2006D-0331 | Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors; Exception from Informed Consent Requirements for Emergency Research | |||||||||||||||||||||||
| FDA Comment Number : | EC4 | |||||||||||||||||||||||
| Submitter : | Mr. William Martin | Date & Time: | 09/11/2006 10:09:40 | |||||||||||||||||||||
| Organization : | Citizen of The United States | |||||||||||||||||||||||
| Category : | Individual Consumer | |||||||||||||||||||||||
| Issue Areas/Comments | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| GENERAL | ||||||||||||||||||||||||
| This proposed change in "INFORMED CONSENT",via no INFORMED CONSENT, is NAZI-LIKE.Medical Nazism.Does the United States Government forsee a time ,probably soon,when they will need to forcefully subject invalid citizens,and probably then other citizens,to strange experimental treatments and procedures?Will every medical facility have a "MENGELE DOC"? Maybe some of these horror movies are about to come to life."What beast slinks toward Bethlehem" W.M.
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