- DARKROOM BOOTH LAYER LOCKED WHEN NOT LOCKED MANUAL
- DARKROOM BOOTH LAYER LOCKED WHEN NOT LOCKED PORTABLE
The results of those evaluations and any corrective actions taken must be retained for a period of time equal to at least the facility's inspection interval. The results of the evaluation must be compared to the manufacturer's published specifications for that type of device. The graphs shall be kept for a period of time equal to at least the facility's inspection interval.įacilities using dry image processing devices must evaluate those devices according to the manufacturer's recommended test procedures and test frequencies.
DARKROOM BOOTH LAYER LOCKED WHEN NOT LOCKED MANUAL
Facilities with manual processing must chart these parameters every other day processing is performed or at a minimum of once a week and measure the temperature of the developer each day processing is performed. Each action shall be dated and initialed.įacilities with automatic processors must chart speed, contrast, and base + fog for each day processing is performed. Processor maintenance logs shall include preventive maintenance, corrective maintenance and cleaning. B and H)Ĭontrol charts of sensitometry shall be maintained and used to regulate processing. These measurements shall be repeated when changes are made to the system which effect the radiation output. The facility shall have available the radiation output measurements for common x-ray examinations they perform for patient and staff information for each x-ray unit. Radiation Output Measurements for Common X-ray Examinations (App.Records of repairs and other pertinent data shall also be available
one set of test results from each intervening year to show changes over time. the initial test results (acceptance testing and radiation safety survey as appropriate). Records shall be maintained for each x-ray tube and include: a list of the equipment to be used for testing and. a brief description of the procedures to be used for each test (see Appendix C). the acceptability limits for each test. a list of the tests to be performed and the frequency of performance. The physician or chiropractor who registers the radiation equipment is responsible for radiation safety and quality assurance and the implementation of this program.Įach facility will establish a manual that includes the following items: Radiation Safety/Quality Assurance Responsibility. Radiation Safety/Quality Assurance Program Please note that this program is in addition to and does not replace other sections of Part 16 that pertain to your operations. The Radiation Safety/Quality Assurance requirements are outlined in Sections 16.5 and 16.23 of Part 16 of Chapter 1 of Title 10 (Health) of the Official Compilation of Codes, Rules and Regulations. The statutory authority for these rules and regulations is found in the New York State Public Health Law, Section 225. Equipment problems should be corrected and documented expeditiously and shall be corrected with appropriate documentation within sixty (60) days of discovery. Processor problems need to be addressed as they occur and before the limits are exceeded. The control limits and standards used in this guide have been taken from the Federal Performance Standard for Diagnostic X-ray Equipment, Part 16, and other references listed in the bibliography. The regulations in Part 16 and this guide have been established on the ALARA Principle to assure that the benefits of the use of ionizing radiation exceed the risks to the individual and the public health and safety. ALARA (As Low As Reasonably Achievable). Facilities performing more than 2500 studies each year are referred to the Department's "Guide for Radiation Safety/Quality Assurance Programs". This guide applies to medical and chiropractic facilities performing less than 2500 diagnostic radiographic examinations each year. References can be found in the bibliography to assist you with test procedures and to answer questions not addressed in this brief guide regarding Quality Control and Quality Assurance. Facilities may substitute quality control tests if the tests are deemed equivalent by the Department prior to their implementation. It is important to review the overall program and not become enmeshed in the quality control tests. It is our goal to assist facilities to be more actively involved and responsible for Quality Assurance in their practices. Our Department has implemented this program to reduce radiation exposure and optimize diagnostic x-ray image quality. This guide describes the type and extent of information and standards by which the New York State Department of Health will evaluate a facility's Radiation Safety/Quality Assurance Program. DARKROOM BOOTH LAYER LOCKED WHEN NOT LOCKED PORTABLE
Guide for Radiation Safety/Quality Assurance Programs for Small Facilities, Part I - Radiographic Equipment is available in Portable Document Format (PDF, 150KB, 48pg.). Guide for Radiation Safety/Quality Assurance Programs Small Facilities
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