Skip to main content
Back To Top Top Back To Top
This website publishes administrative rules on their effective dates, as designated by the adopting state agencies, colleges, and universities.

Ohio Administrative Code Search

Busy
 
Keywords
:
1-719-323-9442
{"removedFilters":"","searchUpdateUrl":"\/ohio-administrative-code\/search\/update-search","keywords":"1-719-323-9442","start":4176,"pageSize":25,"sort":"BestMatch"}
Results 4,176 - 4,200 of 10,288
Sort Options
Sort Options
Rules
Rule
Rule 3701:1-58-85 | Records of molybdenum-99, strontium-82, and strontium-85 concentrations.

...ts required by paragraph (B) of rule 3701:1-58-35 of the Administrative Code for three years. The record must include: (A) For each measured elution of technetium-99m, the ratio of the measures expressed as kilobecquerel (microcuries) of molybdenum-99 per megabecquerel (millicurie) of technetium-99m, the time and date of the measurement, and the name of the individual who made the measurement; or (B) For each measu...

Rule 3701:1-58-86 | Records of safety instruction.

...afety instructions required by rules 3701:1-58-38, 3701:1-58-46, and 3701:1-58-58 of the Administrative Code for three years. The record must include a list of the topics covered, the date of the instruction, the name(s) of the attendee(s), and the name(s) of the individual(s) who provided the instruction.

Rule 3701:1-58-86 | Records of safety instruction.

...ety instructions required by rules 3701:1-58-38, 3701:1-58-46 of the Administrative Code, and the operational and safety instructions required by rule 3701:1-58-58 of the Administrative Code, for three years. The record must include a list of the topics covered, the date of the instruction, the name(s) of the attendee(s), and the name(s) of the individual(s) who provided the instruction.

Rule 3701:1-58-87 | Records of surveys after source implant and removal.

...ord of the surveys required by rules 3701:1-58-44 and 3701:1-58-56 of the Administrative Code for three years. Each record must include the date and results of the survey, the survey instrument used, and the name of the individual who made the survey.

Rule 3701:1-58-88 | Records of brachytherapy source accountability.

...urce accountability required by rule 3701:1-58-45 of the Administrative Code for three years. (B) For temporary implants, the record must include: (1) The number and activity of sources removed from storage, the time and date they were removed from storage, the name of the individual who removed them from storage, and the location of use; and (2) The number and activity of sources returned to storage, the time and...

Rule 3701:1-58-89 | Records of calibration measurements of brachytherapy sources.

...achytherapy sources required by rule 3701:1-58-48 of the Administrative Code for three years after the last use of the source. (B) The record must include: (1) The date of the calibration; (2) The manufacturer's name, model number, and serial number for the source and the instruments used to calibrate the source; (3) The source output or activity; (4) The source positioning accuracy within the applicators; and ...

Rule 3701:1-58-90 | Records of decay of strontium-90 sources for ophthalmic treatments.

...strontium-90 source required by rule 3701:1-58-49 of the Administrative Code for the life of the source. (B) The record must include: (1) The date and initial activity of the source as determined under rule 3701:1-58-48 of the Administrative Code; and (2) For each decay calculation, the date and the source activity as determined under rule 3701:1-58-49 of the Administrative Code.

Rule 3701:1-58-91 | Records of installation, maintenance, adjustment, and repair of remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

...diosurgery units as required by rule 3701:1-58-57 of the Administrative Code for three years. For each installation, maintenance, adjustment and repair, the record must include the date, description of the service, and name(s) of the individual(s) who performed the work.

Rule 3701:1-58-92 | Records of safety procedures for remote afterloaders, teletherapy units, or gamma stereotactic radiosurgery units.

...paragraphs (A)(4) and (D)(2) of rule 3701:1-58-58 of the Administrative Code until the licensee no longer possesses the remote afterloader, teletherapy unit, or gamma stereotactic radiosurgery unit.

Rule 3701:1-58-93 | Records of dosimetry equipment used with remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

...uipment done in accordance with rule 3701:1-58-60 of the Administrative Code for the duration of the license. (B) For each calibration, intercomparison, or comparison, the record must include: (1) The date; (2) The manufacturer's name, model numbers and serial numbers of the instruments that were calibrated, intercompared, or compared as required by paragraphs (A) and (B) of rule 3701:1-58-60 of the Administrative...

Rule 3701:1-58-94 | Records of full calibrations for teletherapy units, remote afterloader units, and gamma stereotactic radiosurgery units.

... full calibrations required by rules 3701:1-58-61 to 3701:1-58-63 of the Administrative Code for three years. (B) The record must include: (1) The date of the calibration; (2) The manufacturer's name, model number, and serial number of the teletherapy, remote afterloader, and gamma stereotactic radiosurgery unit(s), the source(s), and the instruments used to calibrate the unit(s); (3) The results and an assessmen...

Rule 3701:1-58-95 | Records of periodic spot-checks for teletherapy units.

...r teletherapy units required by rule 3701:1-58-64 of the Administrative Code for three years. (B) The record must include: (1) The date of the spot-check; (2) The manufacturer's name, model number, and serial number of the teletherapy unit, source and instrument used to measure the output of the teletherapy unit; (3) An assessment of timer linearity and constancy; (4) The calculated on-off error; (5) A determin...

Rule 3701:1-58-96 | Records of periodic spot-checks for remote afterloader units.

...e afterloader units required by rule 3701:1-58-65 of the Administrative Code for three years. (B) The record must include, as applicable: (1) The date of the spot-check; (2) The manufacturer's name, model number, and serial number for the remote afterloader unit and source; (3) An assessment of timer accuracy; (4) Notations indicating the operability of each entrance door electrical interlock, radiation monitors...

Rule 3701:1-58-97 | Records of periodic spot-checks for gamma stereotactic radiosurgery units.

... radiosurgery units required by rule 3701:1-58-66 of the Administrative Code for three years. (B) The record must include: (1) The date of the spot-check; (2) The manufacturer's name, model number, and serial number for the gamma stereotactic radiosurgery unit and the instrument used to measure the output of the unit; (3) An assessment of timer linearity and accuracy; (4) The calculated on-off error; (5) A dete...

Rule 3701:1-58-98 | Records of additional technical requirements for mobile remote afterloader units.

...e afterloader units required by rule 3701:1-58-67 of the Administrative Code for three years. (B) The record must include: (1) The date of the check; (2) The manufacturer's name, model number, and serial number of the remote afterloader unit; (3) Notations accounting for all sources before the licensee departs from a facility; (4) Notations indicating the operability of each entrance door electrical interlock, r...

Rule 3701:1-58-99 | Records of surveys of therapeutic treatment units.

...t units made in accordance with rule 3701:1-58-68 of the Administrative Code for the duration of use of the unit. (B) The record must include: (1) The date of the measurements; (2) The manufacturer's name, model number and serial number of the treatment unit, source, and instrument used to measure radiation levels; (3) Each dose rate measured around the source while the unit is in the off position and the average...

Rule 3701:1-58-100 | Records of five-year inspection for teletherapy and gamma stereotactic radiosurgery units.

... radiosurgery units required by rule 3701:1-58-69 of the Administrative Code for the duration of use of the unit. (B) The record must contain: (1) The inspector's radioactive materials license number; (2) The date of inspection; (3) The manufacturer's name and model number and serial number of both the treatment unit and source; (4) A list of components inspected and serviced, and the type of service; and (5) T...

Rule 3701:1-58-100 | Records of full-inspection servicing for teletherapy and gamma stereotactic radiosurgery units.

... radiosurgery units required by rule 3701:1-58-69 of the Administrative Code for the duration of use of the unit. (B) The record must contain: (1) The inspector's radioactive materials license number; (2) The date of inspection; (3) The manufacturer's name and model number and the serial number of both the treatment unit and source; (4) A list of components inspected and serviced, and the...

Rule 3701:1-58-103 | Report of a leaking source.

...days if a leak test required by rule 3701:1-58-27 of the Administrative Code reveals the presence of one hundred eighty-five becquerels (0.005 microcurie) or more of removable contamination. The report must be filed with the address listed in rule 3701:1-40-04 of the Administrative Code. The written report must include the model number and serial number if assigned, of the leaking source; the radionuclide and its e...

Rule 3701:1-58-104 | Training for the parenteral administration of unsealed radioactive material requiring a written directive.

...(A) Except as provided in rule 3701:1-58-21 of the Administrative Code, the licensee shall require an authorized user for the parenteral administration of unsealed radioactive material requiring a written directive, to be a physician who: (1) Is an authorized user under rule 3701:1-58-40 of the Administrative Code for uses listed in paragraph (B)(1)(b)(vi)(c) or (B)(1)(b)(vi)(d) of rule 3701:1-58-40 of the Administr...

Rule 3701:1-58-104 | Training for the parenteral administration of unsealed radioactive material requiring a written directive.

...(A) Except as provided in rule 3701:1-58-21 of the Administrative Code, the licensee shall require an authorized user for the parenteral administration of unsealed radioactive material requiring a written directive, to be a physician who: (1) Is an authorized user under rule 3701:1-58-40 of the Administrative Code for uses listed in paragraph (B)(1)(b)(vi)(c) of rule 3701:1-58-40 of the Administr...

Rule 3701:1-58-105 | Report and notification for an eluate exceeding permissible molybdenum-99, strontium-82, and strontium-85 concentrations.

...ify by telephone the department at 614-644-2727 and the distributor of the generator within seven calendar days after discovery that an eluate exceeded the permissible concentration listed in paragraph (A) of rule 3701:1-58-35 of the Administrative Code at the time of generator elution. The telephone report to the department must include the manufacturer, model number, and serial number (or lot nu...

Rule 3701:1-66-01 | Definitions.

...(A) As used in this chapter: (1) "Air kerma" means the sum of the initial kinetic energy of all charged ionizing particles liberated by uncharged ionizing radiation in a given mass of air. The unit for air kerma is joules per kilogram which is given the special name of gray (Gy). To determine air kerma in Gy from exposure in units of roentgens (R) multiply exposure by the conversion factor 0.0087...

Rule 3701:1-66-02 | General administration requirements for medical radiation-generating equipment.

...ce. (B) Except as specified in rule 3701:1-66-17 of the Administrative Code, no individual shall be exposed to the useful beam except a patient for dental or medical radiologic procedures and unless such exposure has been authorized by a licensed practitioner within his or her scope of practice. This provision specifically prohibits deliberate exposure for the following purposes: (1) Exposure of an individual for t...

Rule 3701:1-66-02 | General administration obligations for medical radiation-generating equipment.

... Code. (C) The handler will assure: (1) Every individual who performs radiologic procedures on human beings holds the appropriate radiologic license as obligated by Chapter 3701-72 of the Administrative Code and Chapter 4715. of the Revised Code. (2) Every individual who is licensed to perform radiologic procedures is adequately instructed in the registrant's safe operating procedures and can ...