Ohio Administrative Code Search
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Rule 3701:1-58-13 | Radiation protection program changes.
...m without the director's approval if: (1) The revision does not require a license amendment under rule 3701:1-58-08 of the Administrative Code; (2) The revision is in compliance with the regulations and the license; (3) The revision has been reviewed and approved by the radiation safety officer and licensee management; and (4) The affected individuals are instructed on the revised program before the changes are i... |
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Rule 3701:1-58-14 | Supervision.
...rized user, as allowed by paragraph (B)(1) of rule 3701:1-58-06 of the Administrative Code, shall: (1) In addition to the requirements in rule 3701:1-38-10 of the Administrative Code, instruct the supervised individual in the licensee's written radiation protection procedures, written directive procedures, regulations of this chapter, and license conditions with respect to the use of radioactive material; and (2) ... |
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Rule 3701:1-58-15 | Written directives.
...ser before the administration of iodine-131 sodium iodide greater than 1.11 megabecquerels (thirty microcuries), any therapeutic dosage of unsealed radioactive material or any therapeutic dose of radiation from radioactive material. If, because of the emergent nature of the patient's condition, a delay in order to provide a written directive would jeopardize the patient's health, an oral directive is acceptable. Th... |
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Rule 3701:1-58-15 | Written directives.
...ser before the administration of iodine-131 sodium iodide greater than 1.11 megabecquerels (thirty microcuries), any therapeutic dosage of unsealed radioactive material or any therapeutic dose of radiation from radioactive material. If, because of the emergent nature of the patient's condition, a delay in order to provide a written directive would jeopardize the patient's health, an oral directive... |
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Rule 3701:1-58-16 | Procedures for administrations requiring a written directive.
...ures to provide high confidence that: (1) The patient's or human research subject's identity is verified before each administration; and (2) Each administration is in accordance with the written directive. (B) At a minimum, the procedures required by paragraph (A) of this rule must address the following items that are applicable to the licensee's use of radioactive material: (1) Verifying the identity of the pati... |
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Rule 3701:1-58-16 | Procedures for administrations requiring a written directive.
...ures to provide high confidence that: (1) The patient's or human research subject's identity is verified before each administration; and (2) Each administration is in accordance with the written directive. (B) At a minimum, the procedures required by paragraph (A) of this rule must address the following items that are applicable to the licensee's use of radioactive material: (1) Verifying the ... |
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Rule 3701:1-58-17 | Suppliers for sealed sources or devices for medical use.
... with a license issued under Chapter 3701:1-40 and rules 3701:1-38-02 and 3701:1-46-44 of the Administrative Code or equivalent requirements of the United States nuclear regulatory commission or an agreement state; (B) Sealed sources or devices noncommercially transferred from an individual licensed in accordance with rule 3701:1-58-06 of the Administrative Code or a United States nuclear regulatory commission or ag... |
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Rule 3701:1-58-18 | Training for radiation safety officer and associate radiation safety officer.
...Except as provided in rule 3701:1-58-21 of the Administrative Code, the licensee shall require an individual fulfilling the responsibilities of the radiation safety officer or an individual assigned duties and tasks as an associate radiation safety officer as provided in rule 3701:1-58-12 of the Administrative Code to be an individual who: (A) Is certified by a specialty board whose certification process... |
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Rule 3701:1-58-19 | Training for an authorized medical physicist.
...Except as provided in rule 3701:1-58-21 of the Administrative Code, the licensee shall require the authorized medical physicist to be an individual who: (A) Is certified by a specialty board whose certification process has been recognized by the director, United States nuclear regulatory commission, or an agreement state and who meets the requirements in paragraphs (B)(2) and (C) of this rule. The names of board cer... |
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Rule 3701:1-58-19 | Training for an authorized medical physicist.
...Except as provided in rule 3701:1-58-21 of the Administrative Code, the licensee shall require the authorized medical physicist to be an individual who: (A) Is certified by a specialty board whose certification process has been recognized by the director, the United States nuclear regulatory commission, or an agreement state and who meets the requirements in paragraph (C) of this rule. The names of b... |
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Rule 3701:1-58-20 | Training for an authorized nuclear pharmacist.
...Except as provided in rule 3701:1-58-21 of the Administrative Code, the licensee shall require the authorized nuclear pharmacist to be a pharmacist who: (A) Is certified by a specialty board whose certification process has been recognized by the director, United States nuclear regulatory commission, or an agreement state. The names of board certifications which have been recognized by the director, U... |
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Rule 3701:1-58-21 | Training for experienced radiation safety officer, teletherapy or medical physicist, authorized medical physicist, authorized user, nuclear pharmacist, and authorized nuclear pharmacist.
...(A) (1) An individual identified as a radiation safety officer, a teletherapy or medical physicist, an authorized medical physicist, a nuclear pharmacist or an authorized nuclear pharmacist on a United States nuclear regulatory commission or agreement state license or a permit issued by a United States nuclear regulatory commission or agreement state broad scope licensee or master material lice... |
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Rule 3701:1-58-22 | Recentness of training.
...ng and experience specified in rules 3701:1-58-12 to 3701:1-58-21, 3701:1-58-32 to 3701:1-58-71, and 3701:1-58-104 of the Administrative Code must have been obtained within the seven years preceding the date of application or the individual must have had related continuing education and experience since the required training and experience was completed. |
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Rule 3701:1-58-23 | Possession, use, and calibration of instruments used to measure the activity of unsealed radioactive material.
...ts performed in accordance with rule 3701:1-58-25 of the Administrative Code, a licensee shall possess and use instrumentation to measure the activity of unsealed radioactive material before it is administered to each patient or human research subject. (B) A licensee shall calibrate the instrumentation required in paragraph (A) of this rule in accordance with nationally recognized standards or the manufacturer's ins... |
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Rule 3701:1-58-24 | Calibration of survey instruments.
...liance with this chapter and Chapter 3701:1-38 of the Administrative Code before first use, annually, and following a repair that affects the calibration. A licensee shall: (1) Calibrate all scales with readings up to ten millisievert (one thousand millirem) per hour with a radiation source; (2) Calibrate two separate readings on each scale or decade that will be used to show compliance; and (3) Conspicuously not... |
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Rule 3701:1-58-25 | Determination of dosages of unsealed radioactive material for medical use.
..., this determination must be made by: (1) Direct measurement of radioactivity; or (2) A decay correction, based on the activity or activity concentration determined by: (a) A manufacturer or preparer licensed under rule 3701:1-46-43 of the Administrative Code or equivalent United States nuclear regulatory commission, or agreement state requirements; (b) An United States nuclear regulatory commission, or agreement... |
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Rule 3701:1-58-26 | Authorization for calibration, transmission, and reference sources.
...Any person authorized by rule 3701:1-58-06 of the Administrative Code for medical use of radioactive material may receive, possess, and use any of the following radioactive material for check, calibration, transmission, and reference use: (A) Sealed sources, not exceeding 1.11 gigabecquerels (thirty millicuries) each, manufactured and distributed by a person licensed under rule 3701:1-46-44 of the Administrative Cod... |
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Rule 3701:1-58-26 | Authorization for calibration, transmission, and reference sources.
...A) Any person authorized by rule 3701:1-58-06 of the Administrative Code for medical use of radioactive material may receive, possess, and use any of the following radioactive material for check, calibration, transmission, and reference use: (1) Sealed sources, not exceeding 1.11 gigabecquerels (thirty millicuries) each, manufactured and distributed by a person licensed under rule 3701:1-46-44 of... |
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Rule 3701:1-58-26 | Authorization for calibration, transmission, and reference sources.
...(A) Any person authorized by rule 3701:1-58-06 of the Administrative Code for medical use of radioactive material may receive, possess, and use any of the following radioactive material for check, calibration, transmission, and reference use: (1) Sealed sources, not exceeding 1.11 gigabecquerels (thirty millicuries) each, manufactured and distributed by a person licensed under rule 3701:1-46-44 o... |
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Rule 3701:1-58-27 | Requirements for possession of sealed sources and brachytherapy sources.
... possession of a sealed source shall: (1) Test the source for leakage before its first use unless the licensee has a certificate from the supplier indicating that the source was tested within six months before transfer to the licensee; and (2) Test the source for leakage at intervals not to exceed six months or at other intervals approved by the director, United States nuclear regulatory commission, or an agreemen... |
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Rule 3701:1-58-29 | Surveys of ambient radiation exposure rate.
...n to the surveys required by Chapter 3701:1-38 of the Administrative Code, a licensee shall survey, with a radiation detection survey instrument at the end of each day of use, the following: (1) All areas where unsealed radioactive material requiring a written directive was prepared for use or administered. This includes all unsealed radiopharmaceuticals prepared for use or administered under rule 3701:1-58-37 of t... |
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Rule 3701:1-58-30 | Release of individuals containing unsealed radioactive material or implants containing radioactive material.
...is likely to exceed one millisievert (0.1 rem). If the total effective dose equivalent to a nursing infant or child could exceed one millisievert (0.1 rem) assuming there were no interruption of breast-feeding, the instructions must also include: (1) Guidance on the interruption or discontinuation of breast-feeding; and (2) Information on the potential consequences, if any, of failure to follow the guidance. (C) ... |
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Rule 3701:1-58-30 | Release of individuals containing unsealed radioactive material or implants containing radioactive material.
...ikely to exceed one millisievert (0.1 rem). If the total effective dose equivalent to a nursing infant or child could exceed one millisievert (0.1 rem) assuming there were no interruption of breast-feeding, the instructions must also include: (1) Guidance on the interruption or discontinuation of breast-feeding; and (2) Information on the potential consequences, if any, of failure to follow the ... |
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Rule 3701:1-58-31 | Provision of mobile medical service.
...oviding mobile medical service shall: (1) Obtain a letter signed by the management of each client for which services are rendered that permits the use of radioactive material at the client's address and clearly delineates the authority and responsibility of the licensee and the client; (2) Check instruments used to measure the activity of unsealed radioactive material for proper function before medical use at each ... |
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Rule 3701:1-58-32 | Use of unsealed radioactive material for uptake, dilution, and excretion studies for which a written directive is not required.
...irective under paragraph (B) of rule 3701:1-58-15 of the Administrative Code, a licensee may use any unsealed radioactive material prepared for medical use for uptake, dilution, or excretion studies that is: (A) Obtained from: (1) A manufacturer or preparer licensed under rule 3701:1-46-43 of the Administrative Code or equivalent United States nuclear regulatory commission or agreement state requirements; or (2) A... |