Section 16.101
|
Definitions |
Section 16.102
|
Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency |
Section 16.103
|
IRB membership |
Section 16.107
|
IRB functions and operations |
Section 16.108
|
IRB review of research |
Section 16.109
|
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor |
Section 16.110
|
Criteria for IRB approval of research |
Section 16.111
|
Review by institution |
Section 16.112
|
Suspension or termination of IRB approval of research |
Section 16.113
|
Cooperative research |
Section 16.114
|
IRB records |
Section 16.115
|
General requirements for informed consent |
Section 16.116
|
Documentation of informed consent |
Section 16.117
|
Applications and proposals lacking definite plans for involvement of human subjects |
Section 16.118
|
Research undertaken without the intention of involving human subjects |
Section 16.119
|
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or |
Section 16.120
|
Use of Federal funds |
Section 16.122
|
Early termination of research support: Evaluation of applications and proposals |
Section 16.123
|
Conditions |
Section 16.124
|
Incorporation by reference |