Current through Register Vol. 64, No. 1, January 1, 2025
Section 333-116-0690 - Training for Use of Manual Brachytherapy SourceExcept as provided in OAR 333-116-0740, the licensee must require the authorized user using manual brachytherapy sources specified in OAR 333-116-0420 for therapy to be a physician who:
(1) Is certified by a medical specialty board whose certification process has been recognized by the U.S. Nuclear Regulatory Commission or an Agreement State. The names of board certifications that have been recognized by the U.S. Nuclear Regulatory Commission or an Agreement State are posted on the U.S. Nuclear Regulatory Commission's Medical Uses Licensee Toolkit web page. To have its certification process recognized, a specialty board shall require all candidates for certification to: (a) Successfully complete a minimum of three years of residency training in a radiation oncology program 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(b) Pass an examination, administered by diplomats of the specialty board, that tests knowledge and competence in radiation safety, radionuclide handling, treatment planning, quality assurance and clinical use of manual brachytherapy; or(2) Has completed a structured educational program in basic radionuclide handling techniques applicable to the use of manual brachytherapy sources that includes: (a) 200 hours of classroom and laboratory training in the following areas:(A) Radiation physics and instrumentation;(B) Radiation protection;(C) Mathematics pertaining to the use and measurement of radioactivity; and(D) Radiation biology; and(b) 500 hours of work experience, under the supervision of an authorized user who meets the requirements in OAR 333-116-0690, 333-116-0740 or equivalent U.S. Nuclear Regulatory or Agreement State requirements at a medical facility authorized to use byproduct materials under OAR 333-116-0420. involving: (A) Ordering, receiving and unpacking radioactive materials safely and performing the related radiation surveys;(B) Checking survey meters for proper operation;(C) Preparing, implanting and removing brachytherapy sources;(D) Maintaining running inventories of material on hand;(E) Using administrative controls to prevent a medical event involving the use of byproduct material; and(F) Using emergency procedures to control byproduct material; and(c) Has completed three years of supervised clinical experience in radiation oncology, under an authorized user who meets the requirements in OAR 333-116-0740, 333-116-0690, or equivalent U.S. Nuclear Regulatory Commission or Agreement State requirements, as part of a formal training program approved by the Residency Review Committee for Radiation Oncology 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. This experience may be obtained concurrently with the supervised work experience required by subsection (2)(b) of this rule; and(d) Has obtained written attestation that the individual has satisfactorily completed the requirements in subsections(2)(a), (2)(b) and (2)(c) of this rule and is able to independently fulfill the radiation safety related duties as an authorized user of manual brachytherapy sources for the medical uses authorized under OAR 333-116-0420. The attestation must be obtained from either:(A) A preceptor authorized user who meets the requirements in OAR 333-116-0690, 333-116-0740, or equivalent U.S. Nuclear Regulatory Commission or Agreement State requirements; 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 OAR 333-116-0690, 333-116-0740 or equivalent U.S. Nuclear Regulatory Commission or Agreement State requirements, 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 subsections (2)(a), (2)(b) and (2)(c) of this rule.Or. Admin. Code § 333-116-0690
HD 1-1991, f. & cert. ef. 1-8-91; PH 12-2006, f. & cert. ef. 6-16-06; PH 4-2007, f. & cert. ef. 3-1-07; PH 14-2008, f. & cert. ef. 9-15-08; PH 4-2010, f. & cert. ef. 2-16-10; PH 4-2013, f. & cert. ef. 1-29-13; PH 14-2013, f. 12-26-13, cert. ef. 1-1-14; PH 24-2014, f. & cert. ef. 8-15-14; PH 69-2018, minor correction filed 02/01/2018, effective 2/1/2018; PH 81-2021, amend filed 11/19/2021, effective 11/23/2021; PH 3-2023, amend filed 01/17/2023, effective 1/18/2023Statutory/Other Authority: ORS 453.635
Statutes/Other Implemented: ORS 453.605 - 453.807