OAR 333-123-0110
Training


(1)

A registrant shall provide instruction, initially and at least annually, to all individuals who operate the electronic brachytherapy device, as appropriate to the individual’s assigned duties, in the operating procedures identified in OAR 333-123-0085 (Operating Procedures). If the interval between patients exceeds one year, retraining of the individuals shall be provided.

(2)

In addition to the requirements of OAR 333-123-0015 (Training and Qualification Requirements for Individuals in the External Beam Radiation Therapy Area)(1) for Radiation Therapy Physicians and OAR 333-123-0015 (Training and Qualification Requirements for Individuals in the External Beam Radiation Therapy Area)(2) for Qualified Medical Physicists, these individuals shall also receive device specific instruction initially from the manufacturer, and annually from either the manufacturer or other qualified trainer. The training shall be of a duration recommended by a recognized national professional association with expertise in electronic brachytherapy (when available). In the absence of any training protocol recommended by a national professional association, the manufacturer’s training protocol shall be followed. The training shall include, but not be limited to:

(a)

Device-specific radiation safety requirements;

(b)

Device operations;

(c)

Clinical use for the types of use approved by the FDA;

(d)

Emergency procedures, including an emergency drill; and

(e)

The registrant’s Quality Assurance Program.

(3)

A registrant shall retain a record of individuals receiving instruction required by this rule for three years. The record shall include:

(a)

A list of the topics covered;

(b)

The date of the instruction;

(c)

The name(s) of the attendee(s); and

(d)

The name(s) of the individual(s) who provided the instruction.
333–123–0001
Purpose and Scope
333–123–0005
Definitions
333–123–0010
General Requirements, Operating Procedures, Surveys, Dosimetry, and Instrument Calibration for Facilities Using Therapeutic Radiation Machines
333–123–0015
Training and Qualification Requirements for Individuals in the External Beam Radiation Therapy Area
333–123–0020
Reports and Notifications of Unplanned Medical Treatment
333–123–0025
Requirements for Therapeutic Radiation Machines
333–123–0030
Facility Design Requirements for Therapeutic Radiation Machines
333–123–0035
Calibration, Acceptance Testing and Commissioning of Therapeutic Radiation Machines
333–123–0040
Quality Assurance And Safety Checks
333–123–0045
Quality Assurance Program
333–123–0050
Qualified Medical Physicist Support in Facilities Having Therapeutic Radiation Machines with Energies of 1 Mv and Above
333–123–0055
Electronic Brachytherapy
333–123–0060
Facility Design Requirements for Electronic Brachytherapy Devices
333–123–0065
Electrical Safety for Electronic Brachytherapy Devices
333–123–0070
Control Panel Functions
333–123–0075
Timer
333–123–0080
Medical Physicist
333–123–0085
Operating Procedures
333–123–0090
Safety Precautions for Electronic Brachytherapy Devices
333–123–0095
Electronic Brachytherapy Source Calibration Measurements
333–123–0100
Periodic and Day-of-Use Quality Assurance Checks for Electronic Brachytherapy Devices
333–123–0105
Therapy Related Computer Systems
333–123–0110
Training
333–123–0115
Mobile Electronic Brachytherapy Service
333–123–0120
Superficial Electronic Brachytherapy
333–123–0125
Superficial Electronic Brachytherapy Personnel Requirements
333–123–0130
Superficial Electronic Brachytherapy: Refresher Training
333–123–0135
Superficial Electronic Brachytherapy: Activation of the Superficial Electronic Brachytherapy X-ray Tube
333–123–0140
Superficial Electronic Brachytherapy: Facility Design Requirements
333–123–0145
Superficial Electronic Brachytherapy: Calibration, Acceptance Testing and Commissioning
333–123–0150
Superficial Electronic Brachytherapy: Quality Assurance Checks
333–123–0155
Superficial Electronic Brachytherapy: Operating Procedures
Last Updated

Jun. 8, 2021

Rule 333-123-0110’s source at or​.us