OAR 333-101-0280
Authority Responsibilities Regarding the Radiology Inspection


The Authority responsibilities must include the following as well as other applicable sections of these rules:

(1)

Do annual audits of hospital programs to monitor accredited radiology inspector results and to monitor changes in the performance of registered X-ray machines during the registration period.

(2)

Evaluate registrant test results provided by the accredited radiology inspectors.

(3)

Grant or deny X-ray machine registrations, accreditation of hospital radiology inspectors and issue documents of registration and accreditation.

(4)

Deny, condition, suspend, or revoke an X-ray machine registration or radiology inspector accreditation.

(5)

Grant a provisional registration permitting temporary operation pending compliance with Authority standards.

(6)

Investigate any alleged prohibited act and resolve complaints against accredited radiology inspectors and their employers.

(7)

Impose civil penalties.

(8)

Develop programs to evaluate hazards associated with the use of X-ray machines.

(9)

Develop testing, training and continued education standards for accreditation of radiology inspectors.

(10)

Promulgate standards and make regulations relating to the registration of X-ray machines, accreditation of radiology inspectors, X-ray machine operation, physical surroundings and equipment related to the operation of the X-ray machines, operator training, and approved X-ray machine operating practices.

(11)

Test applicants for radiology inspector accreditation.

(12)

Collect and disseminate information relating to X-ray machine users.

(13)

Provide technical assistance and safety information to X-ray machine users.

Source: Rule 333-101-0280 — Authority Responsibilities Regarding the Radiology Inspection, https://secure.­sos.­state.­or.­us/oard/view.­action?ruleNumber=333-101-0280.

333‑101‑0001
Purpose and Scope
333‑101‑0003
Definitions
333‑101‑0005
Application for Registration of Radiation Machines
333‑101‑0007
Application for General License Registration for Radioactive Materials Gauges, In Vitro Testing, Source Material, Reference and Calibration Sources, and Reciprocal Recognition of Specific Radioactive Materials License
333‑101‑0010
Exemptions
333‑101‑0015
Transfer or Disposal of Radiation Producing Machines or Equipment
333‑101‑0020
Application for License of Sales, Services, Consultation, and Servicing For Radiation Machines
333‑101‑0023
Application for License of Sales, Consulting Services, and Servicing for Radioactive Materials Devices under General License
333‑101‑0025
Out-of-State Radiation Machines
333‑101‑0035
Issuance of Notice of Registration for X-ray Machines
333‑101‑0040
Expiration of Notice of Registration
333‑101‑0045
Renewal of Notice of Registration
333‑101‑0050
Report of Changes
333‑101‑0055
Approval Not Implied
333‑101‑0060
Assembler and/or Transfer Obligation
333‑101‑0065
Additional Requirements
333‑101‑0070
X-ray Machine Registration Fee Proration
333‑101‑0080
X-ray Machine Registration Denial, Suspension, Revocation and Conditions
333‑101‑0090
Investigation and Civil Penalty
333‑101‑0200
Hospital X-ray Machine Registration
333‑101‑0210
Hospital Radiology Inspector
333‑101‑0220
Hospital Radiology Inspector Qualifications
333‑101‑0230
Hospital Radiology Inspector Testing
333‑101‑0240
Hospital Radiology Inspector Accreditation
333‑101‑0250
Hospital Radiology Inspector Accreditation Revocation
333‑101‑0260
Hospital Radiology Inspector Continuing Education
333‑101‑0270
Hospital Responsibilities Re: X-ray Machines
333‑101‑0280
Authority Responsibilities Regarding the Radiology Inspection
333‑101‑0290
Accredited Hospital Radiology Inspector Responsibilities
Last Updated

Jun. 8, 2021

Rule 333-101-0280’s source at or​.us