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This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.
List of results
- 10 CFR 35 +
- 10 CFR 35.1, Purpose and Scope +
- 10 CFR 35.2, Definitions +
- 10 CFR 35.5, Maintenance of Records +
- 10 CFR 35.6, Provisions for the Protection of Human Research Subjects +
- 10 CFR 35.7, Fda, Other Federal, and State Requirements +
- 10 CFR 35.8, Information Collection Requirements: Omb Approval +
- 10 CFR 35.10, Implementation +
- 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 35.24, Authority and Responsibilities for the Radiation Protection Program +
- 10 CFR 35.26, Radiation Protection Program Changes +
- 10 CFR 35.27, Supervision +
- 10 CFR 35.40, Written Directives +
- 10 CFR 35.41, Procedures for Administrations Requiring a Written Directive +
- 10 CFR 35.49, Suppliers for Sealed Sources Or Devices for Medical Use +
- 10 CFR 35.50, Training for Radiation Safety Officer +
- 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 35.60, Possession, Use, and Calibration of Instruments Used to Measure the Activity of Unsealed Byproduct Material +
- 10 CFR 35.61, Calibration of Survey Instruments +
- 10 CFR 35.63, Determination of Dosages of Unsealed Byproduct Material for Medical Use +
- 10 CFR 35.65, Authorization for Calibration, Transmission, and Reference Sources +
- 10 CFR 35.67, Requirements for Possession of Sealed Sources and Brachytherapy Sources +
- 10 CFR 35.69, Labeling of Vials and Syringes +
- 10 CFR 35.70, Surveys of Ambient Radiation Exposure Rate +
- 10 CFR 35.75, Release of Individuals Containing Unsealed Byproduct Material Or Implants Containing Byproduct Material +
- 10 CFR 35.80, Provision of Mobile Medical Service +
- 10 CFR 35.92, Decay-In-Storage +
- 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 35.190, Training for Uptake, Dilution, and Excretion Studies +
- 10 CFR 35.200, Use of Unsealed Byproduct Material for Imaging and Localization Studies for Which a Written Directive Is Not Required +
- 10 CFR 35.204, Permissible Molybdenum-99, Strontium-82, and Strontium-85 Concentrations +
- 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 35.310, 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 35.400, Use of Sources for Manual Brachytherapy +
- 10 CFR 35.404, Surveys After Source Implant and Removal +
- 10 CFR 35.406, Brachytherapy Sources Accountability +