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(a) In a written directive or prescription.
(b) Under directions of the authorized user for procedures not requiring a written directive.
(269)“Prescribed dose” means any of the following:
(a) For gamma stereotactic radiosurgery, the total dose as documented in the written directive.
(b) For teletherapy, the total dose and dose per fraction as documented in the written directive.
(c) For brachytherapy, either the total source strength and exposure time or the total dose, as documented in the written directive.
(d) For remote afterloaders, the total dose and dose per fraction as documented in the written directive.
(270)“Pressure demand respirator” means a positive pressure atmosphere-supplying respirator that admits breathing air to the facepiece when the positive pressure is reduced inside the facepiece by inhalation.
(271)“Primary dose monitoring system” means a system which will monitor the useful beam during irradiation and which will terminate irradiation when a pre-selected number of dose monitor units have been delivered.
(272)“Primary protective barrier” means the material, excluding filters, placed in the useful beam.
(273)“Principal activities” means activities authorized by the license that are essential to achieving the purpose for which the license was issued or amended. “Principal activities” do not include storage during which no licensed material is accessed for use or disposal and activities incidental to decontamination or decommissioning.
(274)“Product conveyor system” means a system for moving the product to be irradiated to, from and within the area where irradiation takes place.
(275)“Protective apron” means an apron made of radiation absorbing materials used to reduce radiation exposure to the wearer.
(276)“Protective barrier” means a primary or secondary protective barrier of radiation absorbing material or materials used to reduce radiation exposure.
(277)“Protective glove” means a glove made of radiation absorbing materials used to reduce radiation exposure and that surrounds the hand and fingers.
(278)“Public dose” means the dose received by a member of the public from exposure to sources of radiation released by a licensee or registrant or to any other source of radiation under the control of a licensee or registrant. It does not include occupational dose, dose received from background radiation, from any medical administration the individual has received, from exposure to individuals administered radioactive material and released under s. DHS 157.62 (8) or from voluntary participation in medical research programs.
(279)“Pulsed dose-rate remote afterloader” or “PDR” means a device that uses a single source capable of delivering dose rates in the high dose-rate range, but has both of the following characteristics:
(a) Is approximately one-tenth of the activity of typical high dose-rate remote afterloader sources.
(b) Is used to simulate the radiobiology of a low dose rate treatment by inserting the source for a given fraction of each hour.
(279m)“Pulsed mode” means operation of the x-ray system such that the x-ray tube current is pulsed by the x-ray control to produce one or more exposure intervals of duration less than one-half second.
(280)“Pyrophoric liquid” means any liquid that ignites spontaneously in dry or moist air at or below 54.4° C (130° F). This includes spontaneously combustible and water-reactive materials.
(281)“Pyrophoric solid” means any solid material, other than an explosive material, which under normal conditions is liable to cause fires through friction, retained heat from manufacturing or processing, or which may be ignited readily and, when ignited, burns so vigorously and persistently as to create a serious transportation, handling or disposal hazard.
(282)“Qualitative fit test” or “QLFT” means a pass or fail fit test to assess the adequacy of respirator fit that relies on the individual’s response to the test agent.
(283)“Quality control” means an ongoing program to ensure continued reliable performance of the equipment designed to detect changes which may result in a clinically significant degradation in image quality or a significant increase in radiation exposure.
(284)“Quality factor” or “Q” means the modifying factor listed in tables 157.06A and 157.06B of s. DHS 157.06 (4) that is used to derive dose equivalent from absorbed dose.
(285)“Quantitative fit test” or “QNFT” means an assessment of the adequacy of respirator fit by numerically measuring the amount of leakage into the respirator.
(286)“Rad” means the special unit of absorbed dose. One rad is equal to an absorbed dose of 100 erg per gram or 0.01 joule per kilogram (0.01 gray).
(287)“Radiation” means alpha particles, beta particles, gamma rays, x rays, neutrons, high-speed electrons, high-speed protons and other particles capable of producing ions. “Radiation” does not include non-ionizing radiation, such as radiowaves or microwaves, visible, infrared or ultraviolet light.
(288)“Radiation area” means any area, accessible to individuals, in which radiation levels could result in an individual receiving a dose equivalent in excess of 0.05 mSv (0.005 rem) in one hour at 30 centimeters from the source of radiation or from any surface that the radiation penetrates.
(288m)“Radiation generating device” or “RGD” means any system, device, subsystem, or component thereof, which may generate x-rays or particle radiation between 5 keV and 1 MeV, and not intended for healing arts use for humans or animals. RGD may be fixed or portable with any of the following characteristics:
(a) Mobile-means RGD equipment mounted on a permanent base with wheels and/or casters for moving while completely assembled.
(b) Portable-means RGD equipment designed to be hand-carried.
(c) Stationary-means RGD equipment that is installed or placed in a fixed location.
(d) Transportable-means RGD equipment to be installed in a vehicle or that may be readily disassembled for transport or use in a vehicle.
(289)“Radiation head” means the structure from which the useful beam emerges.
(290)“Radiation incident” means the loss of control of a radioactive source or materials or the unintended exposure of an individual to radiation that exceeds the limits in this chapter.
(291)“Radiation installation” means any location or facility where radiation machines are used or where radioactive material is produced, transported, stored, disposed of or used for any purpose.
(292)“Radiation machine” means any device capable of producing radiation, except those devices with radioactive material as the only source of radiation.
(293)“Radiation room” means a shielded room in which irradiations take place. Underwater irradiators do not have radiation rooms.
(294)“Radiation safety officer” or “RSO” means an individual who has the knowledge and training to apply appropriate radiation regulations and has been assigned the responsibility for the overall radiation safety program by the registrant or licensee and is identified on a registration or a specific license.
(295)“Radiation safety officer for industrial radiography” means an individual with the responsibility for the overall radiation safety program for a licensee or registrant and who meets the requirements of s. DHS 157.44 (2).
(295m)“Radiation safety officer for medical use” means an individual that meets the requirements of s. DHS 157.61 (7) (a) or who is identified as a radiation safety officer on a department, NRC or another agreement state medical use license or other equivalent license or permit recognized by the department for similar types and uses of radioactive material.
(296)“Radiation therapy simulation system” means a radiographic, CT or fluoroscopic x-ray system intended for localizing the volume to be exposed during radiation therapy and confirming the position and size of the therapeutic irradiation field.
(297)“Radioactive drug” means any chemical compound containing radioactive material that may be used on or administered to patients or human research subjects as an aid in the diagnosis, treatment or prevention of disease or other abnormal condition.
(298)“Radioactive marker” means radioactive material placed in the well-bore or on a structure intended for subsurface use for the purpose of depth determination or direction orientation.
(299)“Radioactive material” means any solid, liquid or gas that emits radiation spontaneously.
(300)“Radioactivity” means the transformation of unstable atomic nuclei by the emission of radiation.
(301)“Radiograph” means an image which is created directly or indirectly by radiation and results in a permanent record, either film or electronically stored image.
(302)“Radiographer” means any individual who performs or who, in attendance at the site where the sources of radiation are being used, personally supervises industrial radiographic operations and who is responsible to the licensee or registrant for assuring compliance with the requirements of this chapter and the conditions of the license or registration.
(303)“Radiographer certification” means written approval received from a certifying entity stating that an individual has satisfactorily met the equivalent radiation safety, testing and experience criteria in s. DHS 157.44 (3) (a).
(304)“Radiographer’s assistant” means any individual who under the direct supervision of a radiographer, uses radiographic exposure devices, sources of radiation, related handling tools or radiation survey instruments in industrial radiography.
(305)“Radiographic exposure device” means any instrument containing a sealed source fastened or contained within the instrument, in which the sealed source or shielding thereof may be moved or otherwise changed, from a shielded to unshielded position for purposes of making a radiographic exposure.
(306)“Radiographic imaging system” means any system whereby a permanent or semi-permanent image is recorded on an image receptor by the action of ionizing radiation.
(307)“Radiographic operations” means all activities performed with a radiographic exposure device or with a radiation machine. Activities include using, transporting, except by common or contract carriers or storing at a temporary job site, performing surveys to confirm the adequacy of boundaries, setting up equipment and any activity inside restricted area boundaries. Transporting a radiation machine is not considered a radiographic operation.
(308)“Radionuclide” means a radioactive form of an element.
(309)“Rating” means the operating limits as specified by the component manufacturer.
(310)“Redundant beam monitoring system” means a combination of 2 dose monitoring systems in which each system is designed to terminate irradiation under a pre-selected number of dose monitor units.
(311)“Reference man” means a hypothetical aggregation of human physical and physiological characteristics determined by international consensus. These characteristics may be used by researchers and public health workers to standardize results of experiments and to relate biological insult to a common base.
(312)“Reference plane” means a plane that is displaced from and parallel to the tomographic plane.
(313)“Regulations of the U.S. Department of Transportation” means the regulations in 49 CFR 100 to 189 and 390 to 397.
(314)“Rem” means the special unit of any of the quantities expressed as dose equivalent.
Note: The dose equivalent in rem is equal to the absorbed dose in rad multiplied by the quality factor. One rem equals 0.01 sievert.
(315)“Research and development” means either of the following:
(a) Theoretical analysis, exploration or experimentation.
(b) The practical application of investigative findings and theories of a scientific or technical nature for experimental and demonstration purposes, including the experimental production and testing of models, devices, equipment, materials and processes. Research and development does not include the internal or external administration of radiation or radioactive material to human beings.
(316)“Residual radioactivity” means radioactivity in structures, materials, soils, groundwater and other media at a site resulting from activities under the licensee’s or registrant’s control. “Residual radioactivity” includes radioactivity from all sources used by the licensee or registrant, but excludes background radiation. “Residual radioactivity” also includes radioactive materials remaining at the site as a result of routine or accidental releases of radioactive material at the site and previous burials at the site, even if those burials were made in accordance with the provisions of this chapter.
(317)“Respiratory protective equipment” means an apparatus, such as a respirator, used to reduce an individual’s intake of airborne radioactive materials.
(318)“Restricted area” means an area, access to which is limited by the licensee or registrant for the purpose of protecting individuals against undue risks from exposure to sources of radiation. “Restricted area” does not include areas used as residential quarters, but separate rooms in a residential building may be set apart as a restricted area.
(318m)“Reviewing official” means the individual who shall make the trustworthiness and reliability determination of an individual to determine whether the individual may have, or continue to have, unescorted access to the category 1 or category 2 quantities of radioactive materials that are possessed by the licensee.
(319)“Roentgen” or “R” means the special unit of exposure. One roentgen equals 2.58E-4 coulombs per kilogram of air.
Note: See the definition of the term “exposure” and also s. DHS 157.06 (4) for a further explanation of units of exposure.
(319g)“Sabotage” means the act of any person who intentionally damages, interferes, or tampers with reasonable grounds to believe his or her act will hinder, delay, or interfere with the normal operation of any one of the following:
(a) A category 1 or category 2 quantity of radioactive material.
(b) A device that contains a category 1 or category 2 quantity of radioactive material.
(c) The components of the security system.
(319r)“Safe haven” means a readily recognizable and readily accessible site at which security is present or from which, in the event of an emergency, the transport crew can notify and wait for the local law enforcement authorities.
(320)“Sanitary sewerage” means a system of public sewers for carrying off wastewater and refuse, but excluding sewage treatment facilities, septic tanks and leach fields owned or operated by the licensee or registrant.
(321)“Scan” means the complete process of collecting x-ray transmission data for the production of a tomogram. Data may be collected simultaneously during a single scan for the production of one or more tomograms.
(322)“Scan increment” means the amount of relative displacement of the patient with respect to the CT x-ray system between successive scans measured along the direction of such displacement.
(323)“Scan sequence” means a pre-selected set of 2 or more scans performed consecutively under pre-selected CT conditions of operation.
(324)“Scan time” means the period of time between the beginning and end of x-ray transmission data accumulation for a single scan.
(325)“Scattered radiation” means ionizing radiation emitted by interaction of ionizing radiation with matter, the interaction being accompanied by a change in direction of the radiation.
(326)“SCO-I” means a surface contaminated object (SCO) for which all of the following apply:
(a) The non-fixed contamination on the accessible surface averaged over 300 cm2 (or the area of the surface if less than 300 cm2) does not exceed 4 Bq/cm2 (10 -4  microcurie/cm2) for beta and gamma and low toxicity alpha emitters, or 0.4 Bq/cm2 (10-5 microcurie/cm2) for all other alpha emitters.
(b) The fixed contamination on the accessible surface averaged over 300 cm2 (or the area of the surface if less than 300 cm2) does not exceed 4x104 Bq/cm2 (1.0 microcurie/cm2) for beta and gamma and low toxicity alpha emitters, or 4x103 Bq/cm2 (0.1 microcurie/cm2) for all other alpha emitters.
(c) The non-fixed contamination plus the fixed contamination on the inaccessible surface averaged over 300 cm2 (or the area of the surface if less than 300 cm2) does not exceed 4x104 Bq/cm2 (1.0 microcurie/cm2) for beta and gamma and low toxicity alpha emitters, or 4x103 Bq/cm2 (0.1 microcurie/cm2) for all other alpha emitters.
(327)“SCO-II” means a surface contaminated object (SCO) for which the limits for SCO-1 are exceeded and on which all of the following apply:
(a) The non-fixed contamination on the accessible surface averaged over 300 cm2 (or the area of the surface if less than 300 cm2) does not exceed 400 Bq/cm2 (10 -2 microcurie/cm2) for beta and gamma and low toxicity alpha emitters, or 40 Bq/cm2 (10 -3 microcurie/cm2) for all other alpha emitters.
(b) The fixed contamination on the accessible surface averaged over 300 cm2 (or the area of the surface if less than 300 cm2) does not exceed 8x105 Bq/cm2 (20 microcurie/cm2) for beta and gamma and low toxicity alpha emitters, or 8x104 Bq/cm2 (2 microcurie/cm2) for all other alpha emitters.
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Published under s. 35.93, Stats. Updated on the first day of each month. Entire code is always current. The Register date on each page is the date the chapter was last published.