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WAC Sections |
246-235-001 | Purpose and scope. |
246-235-010 | Filing application for specific licenses. |
246-235-020 | General requirements for the issuance of specific licenses. |
246-235-030 | Issuance of specific licenses. |
246-235-040 | Expiration of licenses. |
246-235-050 | Renewal of license. |
246-235-055 | Precedence of license condition over regulation. |
246-235-060 | Amendment of licenses at request of licensee. |
246-235-070 | Agency action on applications to renew or amend. |
246-235-075 | Financial assurance and recordkeeping for decommissioning. |
246-235-077 | Special requirements for emergency planning. |
246-235-080 | Special requirements for possession and use of medical calibration and reference sources. |
246-235-082 | Special requirements for issuance of a specific license to initially transfer source material. |
246-235-083 | Conditions of licenses to initially transfer source material for use under general license—Quality control, labeling, safety instructions, and reports and records. |
246-235-084 | Special requirements for issuance of specific licenses for industrial radiography. |
246-235-085 | Special requirements for issuance of a specific license for wireline services. |
246-235-086 | Special requirements for environmentally significant licensing actions. |
246-235-090 | Special requirements for specific licenses of broad scope. |
246-235-091 | Manufacture and distribution of industrial products containing depleted uranium under general license. |
246-235-093 | Manufacture, assembly or distribution of devices under general license. |
246-235-095 | Manufacture, assembly, or distribution of luminous safety devices, certain calibration sources or ice detectors under general license. |
246-235-097 | Manufacture and distribution of radioactive material for certain in vitro clinical or laboratory testing under general license. |
246-235-100 | Manufacture, production, preparation, or transfer of radiopharmaceuticals for medical use. |
246-235-102 | Manufacture and distribution of sources or devices containing radioactive material for medical use. |
246-235-103 | Prototype tests for manufacture of calibration or reference sources containing americium-241 or radium-226. |
246-235-105 | Manufacture, assembly or distribution of radioactive material exempt from regulation. |
246-235-107 | Serialization of nationally tracked sources. |
246-235-108 | Sealed source and device registration and inactivation. |
246-235-110 | Special requirements for issuance of specific licenses for source material milling. |
246-235-125 | Special requirements to report transactions involving nationally tracked sources. |
246-235-130 | Appendix—General laboratory rules for safe use of unsealed sources. |
246-235-140 | Schedule B, limits for broad licenses. |
246-235-150 | Schedule C—Quantities of radioactive materials requiring consideration of the need for an emergency plan for responding to a release. |
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246-235-120 | Schedule A groups of medical uses of radioactive material (ref. WAC 246-235-080(3) and 246-235-100(9)). [Statutory Authority: RCW 70.98.050. WSR 98-13-037, § 246-235-120, filed 6/8/98, effective 7/9/98. Statutory Authority: RCW 70.98.050 and 70.98.080. WSR 91-15-112 (Order 184), § 246-235-120, filed 7/24/91, effective 8/24/91. Statutory Authority: RCW 43.70.040. WSR 91-02-049 (Order 121), recodified as § 246-235-120, filed 12/27/90, effective 1/31/91. Statutory Authority: RCW 70.98.080. WSR 87-01-031 (Order 2450), § 402-22-200, filed 12/11/86. Statutory Authority: RCW 70.98.050. WSR 81-01-011 (Order 1570), § 402-22-200, filed 12/8/80. Statutory Authority: RCW 70.98.080. WSR 79-12-073 (Order 1459), § 402-22-200, filed 11/30/79, effective 1/1/80. Formerly WAC 402-20-260.] Repealed by WSR 06-05-019, filed 2/6/06, effective 3/9/06. Statutory Authority: RCW 70.98.050. |