10 CFR Subpart A - Subpart A—Exempt Concentrations and Items
- § 32.11 Introduction of byproduct material in exempt concentrations into products or materials, and transfer of ownership or possession: Requirements for license.
- § 32.12 Same: Records and material transfer reports.
- § 32.13 Same: Prohibition of introduction.
- § 32.14 Certain items containing byproduct material; requirements for license to apply or initially transfer.
- § 32.15 Same: Quality assurance, prohibition of transfer, and labeling.
- § 32.16 Certain items containing byproduct material: Records and reports of transfer.
- § 32.18 Manufacture, distribution and transfer of exempt quantities of byproduct material: Requirements for license.
- § 32.19 Same: Conditions of licenses.
- § 32.20 Same: Records and material transfer reports.
- § 32.21 Radioactive drug: Manufacture, preparation, or transfer for commercial distribution of capsules containing carbon-14 urea each for “in vivo” diagnostic use for humans to persons exempt from licensing; Requirements for a license.
- § 32.21a Same: Conditions of license.
- § 32.22 Self-luminous products containing tritium, krypton-85 or promethium-147: Requirements for license to manufacture, process, produce, or initially transfer.
- § 32.23 Same: Safety criteria.
- § 32.24 Same: Table of organ doses.
- § 32.25 Conditions of licenses issued under § 32.22: Quality control, labeling, and reports of transfer.
- § 32.26 Gas and aerosol detectors containing byproduct material: Requirements for license to manufacture, process, produce, or initially transfer.
- § 32.27 Same: Safety criteria.
- § 32.28 Same: Table of organ doses.
- § 32.29 Conditions of licenses issued under § 32.26: Quality control, labeling, and reports of transfer.
- § 32.30 Certain industrial devices containing byproduct material: Requirements for license to manufacture, process, produce, or initially transfer.
- § 32.31 Certain industrial devices containing byproduct material: Safety criteria.
- § 32.32 Conditions of licenses issued under § 32.30: Quality control, labeling, and reports of transfer.