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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 10 - Energy |
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Chapter I - Nuclear Regulatory Commission |
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Part 35 - Medical Use of Byproduct Material |
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Subpart A - General Information |
| § 35.1 - Purpose and scope. |
| § 35.2 - Definitions. |
| § 35.5 - Maintenance of records. |
| § 35.6 - Provisions for the protection of human research subjects. |
| § 35.7 - FDA, other Federal, and State requirements. |
| § 35.8 - Information collection requirements: OMB approval. |
| § 35.10 - Implementation. |
| § 35.11 - License required. |
| § 35.12 - Application for license, amendment, or renewal. |
| § 35.13 - License amendments. |
| § 35.14 - Notifications. |
| § 35.15 - Exemptions regarding Type A specific licenses of broad scope. |
| § 35.18 - License issuance. |
| § 35.19 - Specific exemptions. |