Trial mobile version Guidances- combined files 6_27_14 - page 14

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This is a resource provided by the National Science Foundation that explains the federal
regulations for the protection of human subjects, in an easy-to understand question and answer
format. The questions are organized in the following categories:
The Common Rule and Sub-Parts
Social Science and the Common Rule
Exempt and Expedited Review and Informed Consent
Problems and Advice on Dealing with Them
Confidentiality-Privacy
Ethnography
This document defines ‘engagement’, and the applicable regulations for institutions and programs
receiving funding from the U.S. Department of Education.
This is an informational resource specifically for Institutional Review Boards, created by the U.S.
Food and Drug Administration (FDA). Included is FDA policy regarding IRB Organization,
Membership, Informed Consent and Record-keeping. There is also contact information for FDA
offices.
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