Section 246-240-001. Purpose and scope.

Section 246-240-004. Other federal and state requirements.

Section 246-240-007. Provisions for the protection of human research subjects.

Section 246-240-010. Definitions, abbreviations, and acronyms.

Section 246-240-013. Maintenance of records.

Section 246-240-016. License required.

Section 246-240-019. Application for license, amendment, or renewal.

Section 246-240-022. License amendments.

Section 246-240-025. Notifications.

Section 246-240-028. Exemptions regarding Type A specific licenses of broad scope.

Section 246-240-031. License issuance and specific exemptions.

Section 246-240-051. Authority and responsibilities for the radiation protection program.

Section 246-240-054. Radiation protection program changes.

Section 246-240-057. Supervision.

Section 246-240-060. Written directives.

Section 246-240-063. Procedures for administrations requiring a written directive.

Section 246-240-066. Suppliers for sealed sources or devices for medical use.

Section 246-240-069. Training for radiation safety officer.

Section 246-240-072. Training for an authorized medical physicist.

Section 246-240-075. Training for an authorized nuclear pharmacist.

Section 246-240-078. Training for experienced radiation safety officer, teletherapy or medical physicist, authorized user, and nuclear pharmacist.

Section 246-240-081. Recentness of training.

Section 246-240-101. Possession, use, and calibration of instruments used to measure the activity of unsealed radioactive material.

Section 246-240-104. Calibration of survey instruments.

Section 246-240-107. Determination of dosages of unsealed radioactive material for medical use.

Section 246-240-110. Authorization for calibration, transmission, and reference sources.

Section 246-240-113. Requirements for possession of sealed sources and brachytherapy sources.

Section 246-240-116. Labeling of vials and syringes.

Section 246-240-119. Surveys of ambient radiation exposure rate.

Section 246-240-122. Release of individuals containing unsealed radioactive material or implants containing radioactive material.

Section 246-240-125. Provision of mobile medical service.

Section 246-240-128. Decay-in-storage.

Section 246-240-151. Use of unsealed radioactive material for uptake, dilution, and excretion studies for which a written directive is not required.

Section 246-240-154. Training for uptake, dilution, and excretion studies.

Section 246-240-157. Use of unsealed radioactive material for imaging and localization studies for which a written directive is not required.

Section 246-240-160. Permissible molybdenum-99 concentration.

Section 246-240-163. Training for imaging and localization studies.

Section 246-240-201. Use of unsealed radioactive material for which a written directive is required.

Section 246-240-204. Safety instruction.

Section 246-240-207. Safety precautions.

Section 246-240-210. Training for use of unsealed radioactive material for which a written directive is required.

Section 246-240-213. Training for the oral administration of sodium iodide I-131 requiring a written directive in quantities less than or equal to 1.22 gigabecquerels (33 millicuries).

Section 246-240-216. Training for the oral administration of sodium iodide I-131 requiring a written directive in quantities greater than 1.22 gigabecquerels (33 millicuries).

Section 246-240-219. Training for the parenteral administration of unsealed radioactive material requiring a written directive.

Section 246-240-251. Use of sources for manual brachytherapy.

Section 246-240-254. Surveys after source implant and removal.

Section 246-240-260. Brachytherapy source accountability.

Section 246-240-263. Safety instruction.

Section 246-240-266. Safety precautions.

Section 246-240-269. Calibration measurements of brachytherapy sources.

Section 246-240-272. Decay of strontium-90 sources for ophthalmic treatments.

Section 246-240-275. Therapy-related computer systems.

Section 246-240-278. Training for use of manual brachytherapy sources.

Section 246-240-281. Training for ophthalmic use of strontium-90.

Section 246-240-301. Use of sealed sources for diagnosis.

Section 246-240-304. Training for use of sealed sources for diagnosis.

Section 246-240-351. Use of a sealed source in a remote afterloader unit, teletherapy unit, or gamma stereotactic radiosurgery unit.

Section 246-240-354. Surveys of patients and human research subjects treated with a remote afterloader unit.

Section 246-240-357. Installation, maintenance, adjustment, and repair.

Section 246-240-360. Safety procedures and instructions for remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

Section 246-240-363. Safety precautions for remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

Section 246-240-366. Dosimetry equipment.

Section 246-240-369. Full calibration measurements on teletherapy units.

Section 246-240-372. Full calibration measurements on remote afterloader units.

Section 246-240-375. Full calibration measurements on gamma stereotactic radiosurgery units.

Section 246-240-378. Periodic spot-checks for teletherapy units.

Section 246-240-381. Periodic spot-checks for remote afterloader units.

Section 246-240-384. Periodic spot-checks for gamma stereotactic radiosurgery units.

Section 246-240-387. Additional technical requirements for mobile remote afterloader units.

Section 246-240-390. Radiation surveys.

Section 246-240-393. Five-year inspection for teletherapy and gamma stereotactic radiosurgery units.

Section 246-240-396. Therapy-related computer systems.

Section 246-240-399. Training for use of remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

Section 246-240-501. Other medical uses of radioactive material or radiation from radioactive material.

Section 246-240-551. Records of authority and responsibilities for radiation protection programs.

Section 246-240-554. Records of radiation protection program changes.

Section 246-240-557. Records of written directives.

Section 246-240-560. Records for procedures for administrations requiring a written directive.

Section 246-240-563. Records of calibrations of instruments used to measure the activity of unsealed radioactive material.

Section 246-240-566. Records of radiation survey instrument calibrations.

Section 246-240-569. Records of dosages of unsealed radioactive material for medical use.

Section 246-240-572. Records of leak tests and inventory of sealed sources and brachytherapy sources.

Section 246-240-575. Records of surveys for ambient radiation exposure rate.

Section 246-240-578. Records of the release of individuals containing unsealed radioactive material or implants containing radioactive material.

Section 246-240-581. Records of mobile medical services.

Section 246-240-584. Records of decay-in-storage.

Section 246-240-587. Records of molybdenum-99, strontium-82, and strontium-85 concentrations.

Section 246-240-590. Records of safety instruction.

Section 246-240-593. Records of surveys after source implant and removal.

Section 246-240-596. Records of brachytherapy source accountability.

Section 246-240-599. Records of calibration measurements of brachytherapy sources.

Section 246-240-602. Records of decay of strontium-90 sources for ophthalmic treatments.

Section 246-240-605. Records of installation, maintenance, adjustment, and repair of remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

Section 246-240-608. Records of safety procedures.

Section 246-240-611. Records of dosimetry equipment used with remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

Section 246-240-614. Records of teletherapy, remote afterloader, and gamma stereotactic radiosurgery full calibrations.

Section 246-240-617. Records of periodic spot-checks for teletherapy units.

Section 246-240-620. Records of periodic spot-checks for remote afterloader units.

Section 246-240-623. Records of periodic spot-checks for gamma stereotactic radiosurgery units.

Section 246-240-626. Records of additional technical requirements for mobile remote afterloader units.

Section 246-240-629. Records of surveys of therapeutic treatment units.

Section 246-240-632. Records of five-year inspection for teletherapy and gamma stereotactic radiosurgery units.

Section 246-240-651. Report and notification of a medical event.

Section 246-240-654. Report and notification of a dose to an embryo/fetus or a nursing child.

Section 246-240-657. Report of a leaking source.