United States Government Publishing Office publisher pbl distributor dst United States National Archives and Records Administration Office of the Federal Register author aut Government Organization text government publication eng FR Regulatory Information 2018_register executive 2018-07-14 article Part IV Rules and Regulations D09002ee1c7e4894b D09002ee1c7e48a52 United States Nuclear Regulatory Commission originator org United States Government Agency or Subagency The U.S. Nuclear Regulatory Commission (NRC) is amending its regulations related to the medical use of byproduct material. The final rule will amend the NRC regulations related to the medical use of byproduct material. This rule amends the reporting and notification requirements for a medical event (ME) for permanent implant brachytherapy. This rule also amends the training and experience (T&E) requirements to remove from multiple sections the requirement to obtain a written attestation for an individual who is certified by a specialty board whose certification process has been recognized by the NRC or an Agreement State; and address a request filed in a petition for rulemaking (PRM), PRM-35-20, to exempt certain board-certified individuals from certain T&E requirements (i.e., "grandfather" these individuals). Additionally, this rule amends the requirements for measuring molybdenum contamination; adds a new requirement for the reporting of failed technetium and rubidium generators; and allows licensees to name associate radiation safety officers (ARSOs) on a medical license. 83 FR 33046 https://www.govinfo.gov/app/details/FR-2018-07-16/2018-14852 2018-14852 fr16jy18-12 RIN 3150-AI63 7590-01-P NRC-2008-0175 https://www.govinfo.gov/app/details/FR-2018-07-16/2018-14852 https://www.govinfo.gov/content/pkg/FR-2018-07-16/html/2018-14852.htm https://www.govinfo.gov/content/pkg/FR-2018-07-16/pdf/2018-14852.pdf Byproduct Material Criminal Penalties Government Contracts Intergovernmental Relations Isotopes Nuclear Energy Nuclear Materials Penalties Radiation Protection Reporting and Recordkeeping Requirements Whistleblowing Labeling Biologics Drugs Health Facilities Health Professions Medical Devices Occupational Safety and Health 67 p. 33046 33112 83 FR 33046 Title 10 Part 30 10 CFR Part 30 Title 10 Part 32 10 CFR Part 32 Title 10 Part 35 10 CFR Part 35 RIN 3150-AI63 Medical Use of Byproduct Material-Medical Event Definitions, Training and Experience, and Clarifying Amendments; Federal Register Vol. 83, Issue RULE 2018-14852 IV NUCLEAR REGULATORY COMMISSION 2019-01-14 NRC-2008-0175 7590-01-P 2018-14852 Final rule.

The U.S. Nuclear Regulatory Commission (NRC) is amending its regulations related to the medical use of byproduct material. The final rule will amend the NRC regulations related to the medical use of byproduct material. This rule amends the reporting and notification requirements for a medical event (ME) for permanent implant brachytherapy. This rule also amends the training and experience (T&E) requirements to remove from multiple sections the requirement to obtain a written attestation for an individual who is certified by a specialty board whose certification process has been recognized by the NRC or an Agreement State; and address a request filed in a petition for rulemaking (PRM), PRM-35-20, to exempt certain board-certified individuals from certain T&E requirements (i.e., "grandfather" these individuals). Additionally, this rule amends the requirements for measuring molybdenum contamination; adds a new requirement for the reporting of failed technetium and rubidium generators; and allows licensees to name associate radiation safety officers (ARSOs) on a medical license.

This final rule is effective on January 14, 2019. Kimyata Morgan-Butler, Office of Nuclear Material Safety and Safeguards, U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001, telephone: 301-415-0733, email: Kimyata.Morgan-Butler@nrc.gov. Byproduct Material Criminal Penalties Government Contracts Intergovernmental Relations Isotopes Nuclear Energy Nuclear Materials Penalties Radiation Protection Reporting and Recordkeeping Requirements Whistleblowing Labeling Biologics Drugs Health Facilities Health Professions Medical Devices Occupational Safety and Health Medical Use of Byproduct Material: Medical Event Definitions, Training and Experience, and Clarifying Amendments , Carol.Gallagher@nrc.gov Kimyata.Morgan-Butler@nrc.gov oira_submission@omb.eop.gov pdr.resource@nrc.gov http://www.nrc.gov/reading-rm/adams.html http://www.nrc.gov/reading-rm/doc-collections/acmui/tr http://www.regulations.gov www.regulations.gov Vol. 83, no. 136 Office of the Federal Register, National Archives and Records Administration 2018-07-16 continuing daily deposited born digital 367 p. Table of Contents: AE 2.7: GS 4.107: AE 2.106: KF70.A2 https://www.govinfo.gov/app/details/FR-2018-07-16 P0b002ee19b75b5fd 0097-6326 0042-1219 0364-1406 769-004-00000-9 000582072 f:fr16jy18 https://www.govinfo.gov/app/details/FR-2018-07-16 https://www.govinfo.gov/content/pkg/FR-2018-07-16/pdf/FR-2018-07-16.pdf https://www.govinfo.gov/content/pkg/FR-2018-07-16/xml/FR-2018-07-16.xml fdlp 32759 33117 DGPO 2018-07-14 2024-06-01 FR-2018-07-16 machine generated eng FR FR-2018-07-16 83 136