Fla. Admin. Code Ann. R. 64E-5.6411 - Full Calibration Measurements on Remote Afterloader Units
(1) A licensee
authorized to use a remote afterloader unit for medical use shall perform full
calibration measurements on each remote afterloader unit:
(a) Before the first medical use of the
unit;
(b)
1. Before medical use following replacement
of the source or following reinstallation of the unit in a new location outside
the facility; and
2. Before medical
use following any repair of the unit that includes removal of the source or
major repair of the components associated with the source exposure assembly;
and
(c) At intervals not
exceeding 1 quarter for high dose-rate, medium dose-rate, and pulsed dose-rate
remote afterloader units with sources whose half-life exceeds 75 days;
and
(d) At intervals not exceeding
1 year for low dose-rate remote afterloader units.
(2) Full calibration measurements of remote
afterloader unit shall include the determination of:
(a) The output within 5 percent;
(b) Source positioning accuracy to within 1
millimeter;
(c) Source retraction
with backup battery upon power failure;
(d) Timer constancy and linearity over the
range of use;
(e) Length of the
source transfer tubes;
(f) Length
of the applicators; and
(g)
Function of the source transfer tubes, applicators, and transfer
tube-applicator interfaces.
(3) A licensee shall use the dosimetry system
described in Rule
64E-5.640,
F.A.C., to measure the output for one set of exposure conditions. The remaining
radiation measurements required in paragraph 64E-5.6411(2)(a), F.A.C., may be
made using a dosimetry system that indicates relative dose rates.
(4) A licensee shall make full calibration
measurements required by subsection 64E-5.6411(1), F.A.C., in accordance with
published protocols accepted by nationally recognized bodies.
(5) A licensee shall correct mathematically
the outputs determined in paragraph 64E-5.6411(2)(a), F.A.C., for physical
decay at intervals consistent with 1 percent physical decay.
(6) Full calibration measurements required by
subsection 64E-5.6411(1), F.A.C., and physical decay corrections required by
subsection 64E-5.6411(5), F.A.C., shall be performed by the authorized medical
physicist.
(7) In addition to the
requirements for full calibrations for low dose-rate remote afterloader units
in subsection 64E-5.6411(2), F.A.C., a licensee shall perform an autoradiograph
of the source(s) to verify inventory and source(s) arrangement at intervals not
exceeding 1 quarter.
(8) For low
dose-rate remote afterloader units, a licensee may use measurements provided by
the source manufacturer that are made in accordance with subsections
64E-5.6411(1) -(5), F.A.C.
(9) A
licensee shall maintain a record of each remote afterloader unit calibration
for three years. The record shall include the following:
(a) The date of the calibration;
(b) The manufacturer's name, model number,
and serial number for both the remote afterloader unit and the
source;
(c) The model numbers and
serial numbers of the instruments used to calibrate the remote afterloader
unit;
(d) The results and an
assessment of the full calibrations.
(e) The results of the autoradiograph
required for low dose-rate remote afterloaders; and
(f) The signature of the authorized medical
physicist.
Notes
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