DHS 157.64(6)(c)2.c.c. Calculating, measuring and safely preparing patient or human research subject dosages. DHS 157.64(6)(c)2.d.d. Using administrative controls to prevent a medical event involving the use of radioactive material. DHS 157.64(6)(c)2.e.e. Using procedures to contain spilled radioactive material safely and using proper decontamination procedures. DHS 157.64(6)(c)2.f.f. Administering dosages to patients or human research subjects, that includes at least 3 cases involving the oral administration of greater than 1.22 Gigabecquerels (33 millicuries) of sodium iodide I-131. DHS 157.64(7)(7) Training for the parenteral administration of unsealed radioactive material requiring a written directive. Except as provided in s. DHS 157.61 (10), a licensee shall require an authorized user for the parenteral administration requiring a written directive to be a physician who meets any of the following requirements: DHS 157.64(7)(a)(a) Is an authorized user under sub. (4) for the specific parenteral uses listed in sub. (4) (b) 2. g., or equivalent NRC or agreement state requirements. DHS 157.64(7)(c)(c) Is certified by a medical specialty board whose certification process has been recognized by the department under s. DHS 157.65 (8) or 157.67 (17) or equivalent NRC or agreement state requirements; and who meets the following requirements: DHS 157.64(7)(c)1.1. Has successfully completed 80 hours of classroom and laboratory training, applicable to parenteral administrations of any radioactive drug that contains a radionuclide that is primarily used for its electron emission, beta radiation characteristics, alpha radiation characteristics, or photon energy of less than 150 keV for which a written directive is required. The training shall include all of the following: DHS 157.64(7)(c)2.2. Has work experience with any radioactive drug that contains a radionuclide that is primarily used for its electron emission, beta radiation characteristics, alpha radiation characteristics, or photon energy of less than 150 keV for which a written directive is required. This work experience shall be under the supervision of an authorized user with experience in parenteral administration under sub. (4) (b) 2. g., for which a written directive is required, and who meets the requirements in sub. (4), s. DHS 157.61 (10), this subsection, or equivalent NRC or agreement state requirements. The supervising authorized user who meets the requirements in sub. (4), this subsection, or equivalent NRC or agreement state requirements, must have experience in administering dosages in the same category or categories as the individual requesting authorized user status. The work experience shall involve all the following: DHS 157.64(7)(c)2.a.a. Ordering, receiving, and unpacking radioactive materials safely, and performing the related radiation surveys. DHS 157.64(7)(c)2.b.b. Performing quality control procedures on instruments used to determine the activity of dosages, and performing checks for proper operation of survey meters. DHS 157.64(7)(c)2.c.c. Calculating, measuring, and safely preparing patient or human research subject dosages. DHS 157.64(7)(c)2.d.d. Using administrative controls to prevent a medical event involving the use of unsealed radioactive material. DHS 157.64(7)(c)2.e.e. Using procedures to contain spilled radioactive material safely, and using proper decontamination procedures. DHS 157.64(7)(c)2.f.f. Administering dosages to patients or human research subjects, that include at least 3 cases involving the parenteral administration of any radioactive drug that contains a radionuclide that is primarily used for its electron emission, beta radiation characteristics, alpha radiation characteristics, or photon energy of less than 150 keV, for which a written directive is required. DHS 157.64(8)(a)(a) Unsealed radioactive material for which a written directive is required. As required by sub. (4) (b) 3., the licensee shall require an authorized user of unsealed radioactive material for the uses authorized under sub. (1) to have obtained written attestation that the individual has successfully completed the requirements in sub. (4) (b) and is able to independently fulfill the radiation safety-related duties as an authorized user for the medical uses authorized under sub. (1) for which the individual is requesting authorized user status. The attestation must be obtained from either of the following: DHS 157.64(8)(a)1.1. A preceptor authorized user who meets the requirements in sub. (4), s. DHS 157.61 (10), or equivalent NRC or agreement state requirements and has experience in administering dosages in the same dosage category or categories as the individual requesting authorized user status. DHS 157.64(8)(a)2.2. A residency program director who affirms in writing that the attestation represents the consensus of the residency program faculty where at least one faculty member is an authorized user who meets the requirements in sub. (4), s. DHS 157.61 (10), or equivalent NRC or agreement state requirements, has experience in administering dosages in the same dosage category or categories as the individual requesting authorized user status, and concurs with the attestation provided by the residency program director. The residency training program must be approved by the Residency Review Committee of the Accreditation Council for Graduate Medical Education or the Royal College of Physicians and Surgeons of Canada or the Council on Postdoctoral Training of the American Osteopathic Association and must include training and experience specified in sub. (4) (b). DHS 157.64(8)(b)(b) Oral administration of sodium iodide I-131 requiring a written directive in quantities less than or equal to 1.22 Gigabecquerels (33 millicuries). As required by sub. (5) (c) 3., the licensee shall require an authorized user of sodium iodide I-131 for oral administration to have obtained written attestation that the individual has successfully completed the requirements in sub. (5) (c), and is able to independently fulfill the radiation safety-related duties as an authorized user for oral administration of less than or equal to 1.22 Gigabecquerels (33 millicuries) of sodium iodide I-131 for medical uses authorized under sub. (1). The attestation must be obtained from either of the following: