Current through Register Vol. 48, 12, December 27, 2024
3.12.1 All
personnel dosimeters, except for direct and indirect reading pocket ionization
chambers and those dosimeters used to measure the dose to any extremity, that
require processing to determine the radiation dose and that are used by
registrants to comply with RHB
3.4, with other applicable
provisions of this regulation, or with conditions specified in a registration
shall be processed and evaluated by a dosimetry processor:
3.12.1.1 Holding current personnel dosimetry
accreditation from the National Voluntary Laboratory Accreditation Program
(NVLAP) of the National Institute of Standards and Technology; and
3.12.1.2 Approved in this accreditation
process for the type of radiation or radiations included in the NVLAP program
that most closely approximates the type of radiation or radiations for which
the individual wearing the dosimeter is monitored.
3.12.2 Exposure of a personnel monitoring
device to deceptively indicate a dose delivered to an individual is
prohibited.
3.12.3 Personnel
Monitoring Devices.
3.12.3.1 Personnel
Monitoring (or other dosimeters approved by the Department) shall meet the
following requirements:
3.12.3.1.1 The
monitoring device shall be assigned to and worn only by one
individual;
3.12.3.1.2 When a
protective apron is worn, the monitoring device shall be worn at the collar,
outside the apron;
3.12.3.1.3 If a
personnel monitoring device is lost or damaged, the Radiation Safety Officer
shall provide a replacement device. If the individual requires monitoring per
RHB 3.12.4, the Radiation
Safety Officer shall calculate the exposure for the time period from issuance
to loss or damage of the device and evaluate the probable radiation exposure to
the worker until a replacement device is issued;
3.12.3.1.4 The Registrant shall ensure that
personnel monitoring devices are returned within forty-five (45) calendar days
of the end of the monitoring period. All dosimeters must be read at least
quarterly, the results from the readings recorded and evaluated for compliance
with RHB
3.3.2 and 3.4, and be available for Departmental
review;
3.12.3.1.5 Documentation
providing explanation of any late, absent, or unused personnel monitoring
devices must be recorded and available for Departmental review;
3.12.3.1.6 Personnel monitoring devices must
be worn in accordance with manufacturer guidelines; and
3.12.3.1.7 Fetal dose dosimeters shall be
read in accordance with
RHB 3.12.6.
3.12.3.2 Control badges are used
to measure background radiation. They shall be stored away from the radiation
area. Control badges are not to be worn as a personnel monitoring device.
Ensure the control badge is returned with the lot of badges with which it was
issued.
3.12.3.3 Upon Departmental
approval, area monitors may be used in place of personnel monitoring
devices.
3.12.4 Each
registrant shall monitor exposures from sources of radiation at levels
sufficient to demonstrate compliance with the occupational dose limits of this
Part. As a minimum:
3.12.4.1 Each registrant
shall monitor occupational exposure to radiation and shall supply and require
the use of individual monitoring devices by:
3.12.4.1.1 Adults likely to receive, in one
(1) year from sources external to the body, a dose in excess of ten percent
(10%) of the limits in
RHB 3.4;
3.12.4.1.2 Minors and declared pregnant women
likely to receive, in one (1) year from sources external to the body, a dose in
excess of ten percent (10%) of any of the applicable limits in
RHB 3.7 or 3.8; and
3.12.4.1.3 Individuals entering a high or
very high radiation area.
3.12.4.1.4 Personnel working with medical
fluoroscopic equipment. 3.12.4.1.5 Such other individuals as the Department
deems necessary.
3.12.5 Determination of Dose
3.12.5.1 When only one (1) individual device
is used and it is located at the neck (collar) outside the protective apron,
the reported deep dose equivalent shall be the effective dose equivalent for
external radiation, except as provided in 3.12.5.2.1.1.
3.12.5.2 The assigned deep dose equivalent
and shallow dose equivalent shall be for the portion of the body receiving the
highest exposure.
3.12.5.2.1 The Radiation
Safety Officer may give consideration that an effective dose equivalent be used
as the permanent record provided that all provisions of
RHB 3.3 are met. When a
protective apron is worn while working with medical fluoroscopic equipment and
monitoring is conducted as specified
RHB 3.12, the effective dose
equivalent for external radiation shall be determined as follows:
3.12.5.2.1.1 When only one (1) individual
monitoring device is used and it is located at the neck (collar) outside the
protective apron, the reported deep dose equivalent value multiplied by 0.3
shall be the effective dose for external radiation; or
3.12.5.2.1.2 When individual monitoring
devices are worn, both under the protective apron at the waist and outside the
protective apron at the neck, the effective dose equivalent for external
radiation shall be assigned the value of the sum of the deep dose equivalent
reported for the individual monitoring device located at the waist under the
protective apron multiplied by 1.5 and the deep dose equivalent reported for
the individual monitoring device located at the neck outside the protective
apron multiplied by 0.04.
3.12.5.2.2 Semi-annual visits shall be made
by the Radiation Safety Officer or his or her designee for personal observation
adherence to proper radiation safety practices. Documentation of these reviews
must be available for Departmental review.
3.12.5.2.3 The Department may immediately
revoke the use of the effective dose equivalent upon determination that a
violation of
RHB 3.12.5 has
occurred.
3.12.5.3
Adjustments to the dose of permanent record shall be determined by the
Radiation Safety Officer prior to any changes to the record. Records of these
actions shall be maintained for Departmental review.
3.12.6 When an individual who has been given
responsibility that involves occupational exposure to x-rays declares that she
is pregnant, the employer must, at her request, provide her with an additional
personnel monitoring device to be worn on the trunk underneath the leaded
apron, when such apron is worn. The fetal badge shall be processed and
evaluated on a monthly basis, at a minimum.