Ohio Administrative Code Search

...Licenses for special nuclear material are of two types: general and specific. The general licenses provided in rules 3701:1-56-02 and 3701:1-56-03 of the Administrative Code are effective without the filing of applications with the director or the issuance of licensing documents to particular persons. Specific licenses are issued to named persons upon applications filed pursuant to rule 3701:1-38-02 of the ...

...(A) Each applicant for a specific license authorizing possession and use of unsealed special nuclear material in quantities specified in paragraph (B) of this rule shall either: (1) Submit a decommissioning funding plan as described in paragraph (C) of this rule; or (2) Submit a certification that financial assurance for decommissioning has been provided in the amount prescribed by paragraph (B) of this rule using ...

...(A) Each specific license expires at the end of the day on the expiration date stated in the license unless the licensee has filed an application for renewal under rule 3701:1-38-02 of the Administrative Code not less than ninety days before the expiration date stated in the existing license. If an application for renewal has been filed at least ninety days before the expiration date stated in the...

...(A) Each specific license expires at the end of the day on the expiration date stated in the license unless the licensee has filed an application for renewal under rule 3701:1-38-02 of the Administrative Code not less than ninety days before the expiration date stated in the existing license. If an application for renewal has been filed at least ninety days before the expiration date stated in the...

...Terms defined in rule 3701:1-38-01 of the Administrative Code shall have the same meaning when used in this chapter except as set out herein unless otherwise specifically defined elsewhere: (A) "Authorized medical physicist" means an individual who: (1) Meets the requirements in paragraph (A) of rule 3701:1-58-19 and rule 3701:1-58-22 of the Administrative Code; or (2) Is identified as an authorized medical physi...

...The terms used in this chapter have the same meaning as found in rule 3701:1-38-01 of the Administrative Code, unless an alternative definition is provided in this rule or in another rules of this chapter: (A) "Associate radiation safety officer" means an individual who: (1) Meets the requirements in rules 3701:1-58-18 and 3701:1-58-22 of the Administrative Code; and (2) Is currently identifi...

...This chapter contains the requirements and provisions for the medical use of radioactive material and for issuance of specific licenses authorizing the medical use of this material. These requirements and provisions provide for the radiation safety of workers, the general public, patients, and human research subjects. The requirements and provisions of this chapter are in addition to, and not in substitution for, o...

...(A) A licensee may conduct research involving human research subjects only if it uses the radioactive materials specified on its license for the uses authorized on its license. (B) If the research is conducted, funded, supported, or regulated by a federal agency that has implemented the federal policy for the protection of human subjects as specified in 45 C.F.R. Part 46, as published in the October 1, 2013, Code of...

...(A) A person may manufacture, produce, acquire, receive, possess, prepare, use, or transfer radioactive material for medical use only in accordance with a specific license issued by the director, United States nuclear regulatory commission, an agreement state, or as allowed in paragraph (B)(1) or (B)(2) of this rule. (B) A specific license is not needed for an individual who: (1) Receives, possesses, uses, or trans...

...(A) An application must be signed by the applicant's or licensee's management as defined in rule 3701:1-38-01 of the Administrative Code. (B) An application for a license for medical use of radioactive material as described in rules 3701:1-58-32, 3701:1-58-34, 3701:1-58-37, 3701:1-58-43, 3701:1-58-53, 3701:1-58-55, and 3701:1-58-72 of the Administrative Code must be made by: (1) Submitting documentation in accordan...

...(A) An application must be signed by the applicant's or licensee's "management," as defined in rule 3701:1-38-01 of the Administrative Code. (B) An application for a license for medical use of radioactive material, as described in rules 3701:1-58-32, 3701:1-58-34, 3701:1-58-37, 3701:1-58-43, 3701:1-58-53, 3701:1-58-55, and 3701:1-58-72 of the Administrative Code, must be made by: (1) Submitting ...

...A licensee shall apply for and must receive a license amendment and pay the invoiced amendment fee specified in rule 3701:1-38-02 of the Administrative Code: (A) Before it receives, prepares, or uses radioactive material for a type of use that is permitted under this chapter, but that is not authorized on the licensee's current license issued under this chapter, and Chapter 3701:1-40 of the Administrative Code; (B)...

...A licensee shall apply for and must receive a license amendment and pay the invoiced amendment fee specified in rule 3701:1-38-02 of the Administrative Code: (A) Before it receives, prepares, or uses radioactive material for a type of use that is permitted under this chapter, but that is not authorized on the licensee's current license issued under this chapter, and Chapter 3701:1-40 of the Administr...

...(A) A licensee shall provide the director a copy of the board certification and the written attestation(s), signed by a preceptor, the United States nuclear regulatory commission or agreement state license, the permit issued by a United States nuclear regulatory commission master material licensee, the permit issued by a United States nuclear regulatory commission or agreement state licensee of broad scope, or the pe...

...(A) A licensee shall provide the director a copy of the board certification and the written attestation(s), signed by a preceptor, the United States nuclear regulatory commission or agreement state license, the permit issued by a United States nuclear regulatory commission master material licensee, the permit issued by a United States nuclear regulatory commission or agreement state licensee of br...

...A licensee possessing a type A specific license of broad scope for medical use, issued under rules 3701:1-40-22 and 3701:1-40-23 of the Administrative Code, is exempt from: (A) The provisions of paragraph (D) of rule 3701:1-58-07 of the Administrative Code regarding the need to file an amendment to the license for medical use of radioactive material, as described in rule 3701:1-58-72 of the Administrative Code; (B)...

...A licensee possessing a type A specific license of broad scope for medical use, issued under rules 3701:1-40-22 and 3701:1-40-23 of the Administrative Code, is exempt from: (A) The provisions of paragraph (D) of rule 3701:1-58-07 of the Administrative Code regarding the need to file an amendment to the license for medical use of radioactive material, as described in rule 3701:1-58-72 of the Administr...

...(A) The director shall issue a license for the medical use of radioactive material if: (1) The applicant has filed documentation in accordance with rule 3701:1-58-07 of the Administrative Code; (2) The applicant has paid any applicable fee as provided in rule 3701:1-38-02 of the Administrative Code; (3) The director finds the applicant equipped and committed to observe the safety standards established by the direc...

...(A) In addition to the radiation protection program requirements of rule 3701:1-38-11 of the Administrative Code, a licensee's management shall approve in writing: (1) Requests for a license application, renewal, or amendment before submittal to the director; (2) Any individual before allowing that individual to work as an authorized user, authorized nuclear pharmacist, or authorized medical physicist; and (3) Rad...

...(A) In addition to the radiation protection program requirements of rule 3701:1-38-11 of the Administrative Code, a licensee's management shall approve in writing: (1) Requests for a license application, renewal, or amendment before submittal to the director; (2) Any individual before allowing that individual to work as an authorized user, authorized nuclear pharmacist, or authorized medical...

...(A) A licensee may revise its radiation protection program 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 i...

...(A) A licensee that permits the receipt, possession, use, or transfer of radioactive material by an individual under the supervision of an authorized 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 procedure...

...(A) A written directive must be dated and signed by an authorized user 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 je...

...(A) A written directive must be dated and signed by an authorized user 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...

...(A) For any administration requiring a written directive, the licensee shall develop, implement, and maintain written procedures 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 th...