10-144-220 Me. Code R. § G-E-392

Current through 2024-51, December 18, 2024
Section 144-220-G-E-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)

Except as provided in G.57, the licensee shall require an authorized user 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), to be a physician who:

A. Is certified by a medical specialty board whose certification process includes all of the requirements in G.392.C(1) and C(2) and whose certification has been recognized by the Agency, the Nuclear Regulatory Commission or an Agreement State Specialty Boards whose certification processes have been recognized by the Agency, Nuclear Regulatory Commission, or Agreement state will be posted on the NRC's Medical Uses Licensee Toolkit Web page; or
B. Is an authorized user under G.390.A and G.390.B, for uses listed in G.390.B(1)(b)(vii)(a) or (b), G.394 or equivalent Nuclear Regulatory Commission or Agreement State requirements; or
C.
(1) Has successfully completed 80 hours of classroom and laboratory training, applicable to the medical use of sodium iodide I-131 for procedures requiring a written directive. The training must include:
(a) Radiation physics and instrumentation;
(b) Radiation protection;
(c) Mathematics pertaining to the use and measurement of radioactivity;
(d) Chemistry of radioactive material for medical use; and
(e) Radiation biology; and
(2) Has work experience, under the supervision of an authorized user who meets the definition of an authorized user in Part A.2 for the same uses or who meets the requirements in G.57, G.390.A, G.390.B, G.392, G.394 or equivalent Nuclear Regulatory Commission or Agreement State requirements. A supervising authorized user who meets the requirements in G.390.B, must have experience in administering dosages as specified in G.390.B(1)(b)(vii)(a) or (b). The work experience must involve:
(a) Ordering, receiving, and unpacking radioactive materials safely and performing the related radiation surveys;
(b) Performing quality control procedures on instruments used to determine the activity of dosages and performing checks for proper operation of survey meters;
(c) Calculating, measuring, and safely preparing patient or human research subject dosages;
(d) Using administrative controls to prevent a medical event involving the use of radioactive material;
(e) Using procedures to contain spilled radioactive material safely and using proper decontamination procedures; and
(f) Administering dosages to patients or human research subjects, that includes at least three cases involving the oral administration of less than or equal to 1.22 gigabecquerels (33 millicuries) of sodium iodide I-131; and
(3) Has obtained written attestation that the individual has satisfactorily completed the requirements in G.392.C(1) and G.392.C(2) of this section, and is able to independently fulfill the radiation safety-related duties as an authorized user for oral administration of less than 1.22 gigabecquerels (33 millicuries) of sodium iodide I-131 for medical uses authorized under G.300. The attestation must be obtained from either:
(a) A preceptor authorized user who meets the requirements in G.57, G.390, G.392, G.394, or equivalent Nuclear Regulatory Commission or Agreement State requirements and has experience in administering dosages as specified in G.390.B(1)(b)(vii)(a) or G.390.B(1)(b)(vii)(b); or
(b) 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 G.57, G.390, G.392, G.394, or equivalent Nuclear Regulatory Commission or Agreement State requirements, has experience in administering dosages as specified in G.390.B(1)(b)(vii)(a) or G.390.B(1)(b)(vii)(b), 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 G.392.C(1) and (2).

10-144 C.M.R. ch. 220, § G-E-392