|
Section 26.101
|
Definitions |
|
Section 26.102
|
Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency |
|
Section 26.103
|
IRB membership |
|
Section 26.107
|
IRB functions and operations |
|
Section 26.108
|
IRB review of research |
|
Section 26.109
|
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor |
|
Section 26.110
|
Criteria for IRB approval of research |
|
Section 26.111
|
Review by institution |
|
Section 26.112
|
Suspension or termination of IRB approval of research |
|
Section 26.113
|
Cooperative research |
|
Section 26.114
|
IRB records |
|
Section 26.115
|
General requirements for informed consent |
|
Section 26.116
|
Documentation of informed consent |
|
Section 26.117
|
Applications and proposals lacking definite plans for involvement of human subjects |
|
Section 26.118
|
Research undertaken without the intention of involving human subjects |
|
Section 26.119
|
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department |
|
Section 26.120
|
Use of Federal funds |
|
Section 26.122
|
Early termination of research support: Evaluation of applications and proposals |
|
Section 26.123
|
Conditions |
|
Section 26.124
|
To what does this subpart apply? |
|
Section 26.201
|
Definitions |
|
Section 26.202
|
Prohibition of research conducted or supported by EPA involving intentional exposure of any human subject who is a |
|
Section 26.203
|
To what does this subpart apply? |
|
Section 26.301
|
Definitions |
|
Section 26.302
|
Duties of IRBs in connection with observational research involving pregnant women and fetuses |
|
Section 26.303
|
Additional protections for pregnant women and fetuses involved in observational research |
|
Section 26.304
|
Protections applicable, after delivery, to the placenta, the dead fetus, or fetal material |
|
Section 26.305
|
To what does this subpart apply? |
|
Section 26.401
|
Definitions |
|
Section 26.402
|
IRB duties |
|
Section 26.403
|
Observational research not involving greater than minimal risk |
|
Section 26.404
|
Observational research involving greater than minimal risk but presenting the prospect of direct benefit to the |
|
Section 26.405
|
Requirements for permission by parents or guardians and for assent by children |
|
Section 26.406
|
To what does this subpart apply? |
|
Section 26.1101
|
Definitions |
|
Section 26.1102
|
IRB membership |
|
Section 26.1107
|
IRB functions and operations |
|
Section 26.1108
|
IRB review of research |
|
Section 26.1109
|
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor |
|
Section 26.1110
|
Criteria for IRB approval of research |
|
Section 26.1111
|
Review by institution |
|
Section 26.1112
|
Suspension or termination of IRB approval of research |
|
Section 26.1113
|
Cooperative research |
|
Section 26.1114
|
IRB records |
|
Section 26.1115
|
General requirements for informed consent |
|
Section 26.1116
|
Documentation of informed consent |
|
Section 26.1117
|
Early termination of research |
|
Section 26.1123
|
Prior submission of proposed human research for EPA review |
|
Section 26.1125
|
To what does this subpart apply? |
|
Section 26.1201
|
Definitions |
|
Section 26.1202
|
Prohibition of research involving intentional exposure of any human subject who is a pregnant woman (and therefore her fetus), |
|
Section 26.1203
|
To what does this subpart apply? |
|
Section 26.1301
|
Definitions |
|
Section 26.1302
|
Submission of information pertaining to ethical conduct of completed human research |
|
Section 26.1303
|
To what does this subpart apply? |
|
Section 26.1501
|
Lesser administrative actions |
|
Section 26.1502
|
Disqualification of an IRB or an institution |
|
Section 26.1503
|
Public disclosure of information regarding revocation |
|
Section 26.1504
|
Reinstatement of an IRB or an institution |
|
Section 26.1505
|
Debarment |
|
Section 26.1506
|
Actions alternative or additional to disqualification |
|
Section 26.1507
|
To what does this subpart apply? |
|
Section 26.1601
|
Definitions |
|
Section 26.1602
|
EPA review of proposed human research |
|
Section 26.1603
|
EPA review of completed human research |
|
Section 26.1604
|
Operation of the Human Studies Review Board |
|
Section 26.1605
|
Human Studies Review Board review of proposed human research |
|
Section 26.1606
|
Human Studies Review Board review of completed human research |
|
Section 26.1607
|
To what does this subpart apply? |
|
Section 26.1701
|
Definitions |
|
Section 26.1702
|
Prohibitions applying to all research subject to this subpart |
|
Section 26.1703
|
Prohibition of reliance on unethical human research with non-pregnant, non-nursing adults |
|
Section 26.1704
|
Prohibition of reliance on unethical human research with non-pregnant, non-nursing adults initiated after April 7, 2006 |
|
Section 26.1705
|
Criteria and procedure for decisions to protect public health by relying on otherwise unacceptable research |
|
Section 26.1706
|
Basis and purpose |