First Page | Document Content | |
---|---|---|
![]() Date: 2005-10-11 13:44:31Medical ethics Design of experiments Pharmacology Research ethics Institutional review board Human subject research Consent Ethical problems using children in clinical trials Informed consent Ethics Clinical research Research | Add to Reading List |
![]() | Summary Table on Subpart D, 45 CFR 46 and 21 CFR 50: Additional DHHS Protections for Children Involved as Subjects in Research; Additional Safeguards for Children in Clinical Investigations (FDA) (Rev, 11/06, 1/07DocID: 17ZWA - View Document |
![]() | Subpart D Additional Protections for Children Involved as Subjects in Research Source: 48 FR 9818, March 8, 1983, unless otherwise noted. §To what do these regulations apply? (a) This subpart applies to all reseaDocID: 17AVf - View Document |
![]() | MDH_IRB FORM 2(A)2012: REVIEW CHECKLISTReview Checklist STUDY PROTOCOL INFORMATIONDocID: 16j9D - View Document |
![]() | A Medical Guide for Youth in Foster Care Got questions?DocID: HU82 - View Document |
![]() | Investigator Checklist for Research Involving Children PROTOCOL TITLE:DocID: FcWV - View Document |