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2018-07-14
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Medical Use of Byproduct Material-Medical Event Definitions, Training and Experience, and Clarifying Amendments
Part IV
Rules and Regulations
D09002ee1bdb8b745
D09002ee1bdb8b80c
United States
Nuclear Regulatory Commission
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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
Code of Federal Regulations
Title 10 Part 30
10 CFR Part 30
Code of Federal Regulations
Title 10 Part 32
10 CFR Part 32
Code of Federal Regulations
Title 10 Part 35
10 CFR Part 35
Regulation Identification Number 3150-AI63
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
Federal Register
Vol. 83, no. 136
Office of the Federal Register, National Archives and Records Administration
2018-07-16
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367 p.
Table of Contents:
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AE 2.106:
KF70.A2
https://www.govinfo.gov/app/details/FR-2018-07-16
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000582072
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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
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2018-07-14
2023-04-28
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