Title 10

PART 35 SUBPART A

Subpart A - General Information

• Atomic Energy Act of 1954, secs. 81, 161, 181, 182, 183, 223, 234, 274 (42 U.S.C. 2111, 2201, 2231, 2232, 2233, 2273, 2282, 2021); Energy Reorganization Act of 1974, secs. 201, 206 (42 U.S.C. 5841, 5846); 44 U.S.C. 3504 note.
• 67 FR 20370, Apr. 24, 2002, unless otherwise noted.

10:1.0.1.1.25.1.94.1	SECTION 35.1	35.1 Purpose and scope.
10:1.0.1.1.25.1.94.2	SECTION 35.2	35.2 Definitions.
10:1.0.1.1.25.1.94.3	SECTION 35.5	35.5 Maintenance of records.
10:1.0.1.1.25.1.94.4	SECTION 35.6	35.6 Provisions for the protection of human research subjects.
10:1.0.1.1.25.1.94.5	SECTION 35.7	35.7 FDA, other Federal, and State requirements.
10:1.0.1.1.25.1.94.6	SECTION 35.8	35.8 Information collection requirements: OMB approval.
10:1.0.1.1.25.1.94.7	SECTION 35.10	35.10 Implementation.
10:1.0.1.1.25.1.94.8	SECTION 35.11	35.11 License required.
10:1.0.1.1.25.1.94.9	SECTION 35.12	35.12 Application for license, amendment, or renewal.
10:1.0.1.1.25.1.94.10	SECTION 35.13	35.13 License amendments.
10:1.0.1.1.25.1.94.11	SECTION 35.14	35.14 Notifications.
10:1.0.1.1.25.1.94.12	SECTION 35.15	35.15 Exemptions regarding Type A specific licenses of broad scope.
10:1.0.1.1.25.1.94.13	SECTION 35.18	35.18 License issuance.
10:1.0.1.1.25.1.94.14	SECTION 35.19	35.19 Specific exemptions.

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