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Category:10 CFR 35
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Pages in category "10 CFR 35"
The following 109 pages are in this category, out of 109 total.
1
- 10 CFR 35.1, Purpose and Scope
- 10 CFR 35.10, Implementation
- 10 CFR 35.100, Use of Unsealed Byproduct Material for Uptake, Dilution, and Excretion Studies for Which a Written Directive Is Not Required
- 10 CFR 35.1000, Other Medical Uses of Byproduct Material Or Radiation From Byproduct Material
- 10 CFR 35.11, License Required
- 10 CFR 35.12, Application for License, Amendment, Or Renewal
- 10 CFR 35.13, License Amendments
- 10 CFR 35.14, Notifications
- 10 CFR 35.15, Exemptions Regarding Type a Specific Licenses of Broad Scope
- 10 CFR 35.18, License Issuance
- 10 CFR 35.19, Specific Exemptions
- 10 CFR 35.190, Training for Uptake, Dilution, and Excretion Studies
- 10 CFR 35.2, Definitions
- 10 CFR 35.200, Use of Unsealed Byproduct Material for Imaging and Localization Studies for Which a Written Directive Is Not Required
- 10 CFR 35.2024, Records of Authority and Responsibilities for Radiation Protection Programs
- 10 CFR 35.2026, Records of Radiation Protection Program Changes
- 10 CFR 35.204, Permissible Molybdenum-99, Strontium-82, and Strontium-85 Concentrations
- 10 CFR 35.2040, Records of Written Directives
- 10 CFR 35.2041, Records for Procedures for Administrations Requiring a Written Directive
- 10 CFR 35.2060, Records of Calibrations of Instruments Used to Measure the Activity of Unsealed Byproduct Material
- 10 CFR 35.2061, Records of Radiation Survey Instrument Calibrations
- 10 CFR 35.2063, Records of Dosages of Unsealed Byproduct Material for Medical Use
- 10 CFR 35.2067, Records of Leaks Tests and Inventory of Sealed Sources and Brachytherapy Sources
- 10 CFR 35.2070, Records of Surveys for Ambient Radiation Exposure Rate
- 10 CFR 35.2075, Records of the Release of Individuals Containing Unsealed Byproduct Material Or Implants Containing Byproduct Material
- 10 CFR 35.2080, Records of Mobile Medical Services
- 10 CFR 35.2092, Records of Decay-In-Storage
- 10 CFR 35.2204, Records of Molybdenum-99, Strontium-82, and Strontium-85 Concentrations
- 10 CFR 35.2310, Records of Safety Instruction
- 10 CFR 35.24, Authority and Responsibilities for the Radiation Protection Program
- 10 CFR 35.2404, Records of Surveys After Source Implant and Removal
- 10 CFR 35.2406, Records of Brachytherapy Source Accountability
- 10 CFR 35.2432, Records of Calibration Measurements of Brachytherapy Sources
- 10 CFR 35.2433, Records of Decay of Strontium-90 Sources for Ophthalmic Treatments
- 10 CFR 35.26, Radiation Protection Program Changes
- 10 CFR 35.2605, Records of Installation, Maintenance, Adjustment, and Repair of Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.2610, Records of Safety Procedures
- 10 CFR 35.2630, Records of Dosimetry Equipment Used With Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.2632, Records of Teletherapy, Remote Afterloader, and Gamma Stereotactic Radiosurgery Full Calibrations
- 10 CFR 35.2642, Records of Periodic Spot-Checks for Teletherapy Units
- 10 CFR 35.2643, Records of Periodic Spot-Checks for Remote Afterloader Units
- 10 CFR 35.2645, Records of Periodic Spot-Checks for Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.2647, Records of Additional Technical Requirements for Mobile Remote Afterloader Units
- 10 CFR 35.2652, Records of Surveys of Therapeutic Treatment Units
- 10 CFR 35.2655, Records of 5-Year Inspection for Teletherapy and Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.27, Supervision
- 10 CFR 35.290, Training for Imaging and Localization Studies
- 10 CFR 35.300, Use of Unsealed Byproduct Material for Which a Written Directive Is Required
- 10 CFR 35.3045, Report and Notification of a Medical Event
- 10 CFR 35.3047, Report and Notification of a Dose to an Embryo/Fetus Or a Nursing Child
- 10 CFR 35.3067, Report of a Leaking Source
- 10 CFR 35.310, Safety Instruction
- 10 CFR 35.315, Safety Precautions
- 10 CFR 35.390, Training for Use of Unsealed Byproduct Material for Which a Written Directive Is Required
- 10 CFR 35.392, 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)
- 10 CFR 35.394, Training for the Oral Administration of Sodium Iodide I-131 Requiring a Written Directive In Quantities Greater Than 1.22 Gigabecquerels (33 Millicuries)
- 10 CFR 35.40, Written Directives
- 10 CFR 35.400, Use of Sources for Manual Brachytherapy
- 10 CFR 35.4001, Violations
- 10 CFR 35.4002, Criminal Penalties
- 10 CFR 35.404, Surveys After Source Implant and Removal
- 10 CFR 35.406, Brachytherapy Sources Accountability
- 10 CFR 35.41, Procedures for Administrations Requiring a Written Directive
- 10 CFR 35.410, Safety Instruction
- 10 CFR 35.415, Safety Precautions
- 10 CFR 35.432, Calibration Measurements of Brachytherapy Sources
- 10 CFR 35.433, Decay of Strontium-90 Sources for Ophthalmic Treatments
- 10 CFR 35.457, Therapy-Related Computer Systems
- 10 CFR 35.49, Suppliers for Sealed Sources Or Devices for Medical Use
- 10 CFR 35.490, Training for Use of Manual Brachytherapy Sources
- 10 CFR 35.491, Training for Ophthalmic Use of Strontium-90
- 10 CFR 35.5, Maintenance of Records
- 10 CFR 35.50, Training for Radiation Safety Officer
- 10 CFR 35.500, Use of Sealed Sources for Diagnosis
- 10 CFR 35.51, Training for an Authorized Medical Physicist
- 10 CFR 35.55, Training for an Authorized Nuclear Pharmacist
- 10 CFR 35.57, Training for Experienced Radiation Safety Officer, Teletherapy Or Medical Physicist, Authorized Medical Physicist, Authorized User, Nuclear Pharmacist, and Authorized Nuclear Pharmacist
- 10 CFR 35.59, Recentness of Training
- 10 CFR 35.590, Training for Use of Sealed Sources for Diagnosis
- 10 CFR 35.6, Provisions for the Protection of Human Research Subjects
- 10 CFR 35.60, Possession, Use, and Calibration of Instruments Used to Measure the Activity of Unsealed Byproduct Material
- 10 CFR 35.600, Use of a Sealed Source In a Remote Afterloader Unit, Teletherapy Unit, Or Gamma Stereotactic Radiosurgery Unit
- 10 CFR 35.604, Surveys of Patients and Human Research Subjects Treated With a Remote Afterloader Unit
- 10 CFR 35.605, Installation, Maintenance, Adjustment, and Repair
- 10 CFR 35.61, Calibration of Survey Instruments
- 10 CFR 35.610, Safety Procedures and Instructions for Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.615, Safety Precautions for Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.63, Determination of Dosages of Unsealed Byproduct Material for Medical Use
- 10 CFR 35.630, Dosimetry Equipment
- 10 CFR 35.632, Full Calibration Measurements On Teletherapy Units
- 10 CFR 35.633, Full Calibration Measurements On Remote Afterloader Units
- 10 CFR 35.635, Full Calibration Measurements On Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.642, Periodic Spot-Checks for Teletherapy Units
- 10 CFR 35.643, Periodic Spot-Checks for Remote Afterloader Units
- 10 CFR 35.645, Periodic Spot-Checks for Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.647, Additional Technical Requirements for Mobile Remote Afterloader Units
- 10 CFR 35.65, Authorization for Calibration, Transmission, and Reference Sources
- 10 CFR 35.652, Radiation Surveys
- 10 CFR 35.655, Five-Year Inspection for Teletherapy and Gamma Stereotactic Radiosurgery Units
- 10 CFR 35.657, Therapy-Related Computer Systems
- 10 CFR 35.67, Requirements for Possession of Sealed Sources and Brachytherapy Sources
- 10 CFR 35.69, Labeling of Vials and Syringes
- 10 CFR 35.690, Reserved
- 10 CFR 35.7, Fda, Other Federal, and State Requirements
- 10 CFR 35.70, Surveys of Ambient Radiation Exposure Rate
- 10 CFR 35.75, Release of Individuals Containing Unsealed Byproduct Material Or Implants Containing Byproduct Material
- 10 CFR 35.8, Information Collection Requirements: Omb Approval
- 10 CFR 35.80, Provision of Mobile Medical Service
- 10 CFR 35.92, Decay-In-Storage