Fla. Admin. Code Ann. R. 64E-5.6331 - Calibration Measurements of Manual Brachytherapy Sources
(1) Before the first medical use of a
brachytherapy source, the licensee shall, using published protocols currently
accepted by nationally recognized bodies, determine the following:
(a) Source output or activity using a
dosimetry system that meets the requirements of subsection
64E-5.640(1),
F.A.C.; and
(b) Source positioning
accuracy within applicators.
(2) Instead of a licensee making its own
measurements as required in subsection 64E-5.6331(1), F.A.C., the licensee may
use measurements provided by the source manufacturer or by a calibration
laboratory accredited by the American Association of Physicists in Medicine
(AAPM) that are made in accordance with subsection 64E-5.6331(1),
F.A.C.
(3) A licensee shall
mathematically correct the outputs or activities determined in subsection
64E-5.6331(1), F.A.C., for physical decay at intervals consistent with 1
percent physical decay.
(4) For
each brachytherapy source the licensee shall retain the following records for
three years after the last use of the source:
(a) The date of calibration;
(b) The manufacturer's name, model number,
and serial number for the source and the instruments used to calibrate the
source;
(c) The source output or
activity;
(d) The source
positioning accuracy within the applicators; and
(e) The name of the individual, the source
manufacturer, or the calibration laboratory that performed the
calibration.
Notes
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.