Current through Register Vol. 63, No. 12, December 1, 2024
Section 333-116-0450 - Brachytherapy Sources Inventory(1) A licensee must maintain accountability at all times for all brachytherapy sources in storage or use.(2) As soon as possible after removing sources from a patient or human research subject, the licensee must return brachytherapy sources to a secure storage area.(3) A licensee must retain the records required in sections (1) and (2) of this rule in accordance with OAR 333-100-0057. (a) For temporary implants, the record must include:(A) The number and activity of sources removed from storage, the time and date they were removed from storage, the name of the individual who removed them from storage, and the location of use; and(B) The number and activity of sources returned to storage, the time and date they were returned to storage, and the name of the individual who returned them to storage.(b) For permanent implants, the record must include: (A) The number and activity of sources removed from storage, the date they were removed from storage, and the name of the individual who removed them from storage;(B) The number and activity of sources not implanted, the date they were returned to storage, and the name of the individual who returned them to storage; and(C) The number and activity of sources permanently implanted in the patient or human research subject.Or. Admin. Code § 333-116-0450
HD 1-1991, f. & cert. ef. 1-8-91; PH 3-2003, f. & cert. ef. 3-27-03; PH 31-2004(Temp), f. & cert. ef. 10-8-04 thru 4-5-05; PH 36-2004, f. & cert. ef. 12-1-04; 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 36-2018, minor correction filed 02/01/2018, effective 2/1/2018Statutory/Other Authority: ORS 453.635
Statutes/Other Implemented: ORS 453.605 - 453.807