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Resources :: Regulations :: Subpart A

Subpart A: Basic HHS Policy for Protection of Human Research Subjects

Sec.

 

46.101

To what does this policy apply?

46.102

Definitions.

46.103

Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency.

46.104-
46.106

[Reserved]

46.107

IRB membership.

46.108

IRB functions and operations.

46.109

IRB review of research.

46.110

Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.

46.111

Criteria for IRB approval of research.

46.112

Review by institution.

46.113

Suspension or termination of IRB approval of research.

46.114

Cooperative research.

46.115

IRB records.

46.116

General requirements for informed consent.

46.117

Documentation of informed consent.

46.118

Applications and proposals lacking definite plans for involvement of human subjects.

46.119

Research undertaken without the intention of involving human subjects.

46.120

Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency.

46.121

[Reserved]

46.122

Use of Federal funds.

46.123

Early termination of research support: Evaluation of applications and proposals.

46.124

Conditions.

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