General Information

  1. Law
  2. CFR 10
  3. Energy
  4. Nuclear Regulatory Commission
  5. Medical Use of Byproduct Material
  6. General Information

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Section
35.1

Purpose and scope.

Section
35.2

Definitions.

Section
35.5

Maintenance of records.

Section
35.6

Provisions for the protection of human research subjects.

Section
35.7

FDA, other Federal, and State requirements.

Section
35.8

Information collection requirements: OMB approval.

Section
35.10

Implementation.

Section
35.11

License required.

Section
35.12

Application for license, amendment, or renewal.

Section
35.13

License amendments.

Section
35.14

Notifications.

Section
35.15

Exemptions regarding Type A specific licenses of broad scope.

Section
35.18

License issuance.

Section
35.19

Specific exemptions.