(i) |
The new or revised regulatory requirement, generic correspondence, staff position, or regulatory guidance, as the staff proposes to disseminate it to licensees or issue it for public comment. The staff should focus on developing less-prescriptive generic actions that are consistent with the NRC's goal of risk-informed and performance-based regulation. The proposed regulatory requirement, generic correspondence, staff position, or regulatory guidance should specify the desired outcome (objective, performance, or result), rather than prescribing how the licensees should attain that outcome. In so doing, the staff should clearly state the desired outcome, such that it (1) is enforceable, and (2) can be achieved by setting readily quantifiable standards that have an unambiguous relationship to a readily measurable quantity. |
(ii) |
Draft documents or other materials supporting the new or revised regulatory requirement, generic correspondence, staff position, or regulatory guidance. (A copy of all materials referenced in the document shall be made available upon request to the CRGR staff. In the event a Committee member requests the CRGR staff to obtain a copy of any reference material for his or her use, copies of the said material will be distributed to all members and will also be retained in the CRGR meeting files.) |
(iii) |
The sponsoring office's position as to whether the proposed regulatory requirement, generic correspondence, staff position, or regulatory guidance would constitute a backfit (that is, whether it would modify, implement, relax existing requirements or staff positions in a manner that would modify or add to systems, structures, or components; the design of a facility; the design approval or manufacturing license for a facility; or the procedures or organization required to design, construct, or operate a facility). |

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(iv) |
The proposed implementation method and resource implications, along with the concurrence (and any comments) of the NRC's Office of the General Counsel (OGC) and all affected offices (including the regional offices), as well as an explanation of any non-concurrences. |
(v) |
The related regulatory analysis, which generally conforms to the directives and guidance of NUREG/BR-0058 and NUREG/BR-0184, as applicable.1 (This does not apply to backfits that ensure compliance or define/redefine adequate protection. For power reactors, a documented evaluation is required, as discussed under item (ix). For nuclear materials, a similar documented evaluation should be provided as part of the CRGR review package.) |
(vi) |
The category of power reactors or nuclear materials facilities or activities to which the proposed regulatory requirement, generic correspondence, staff position, or regulatory guidance applies [i.e., whether it applies only to future plants, operating plants, all pressurized-water reactors (PWRs), all boiling-water reactors (BWRs), specific nuclear steam supply system (NSSS) vendors, specific vintage plants, gaseous diffusion plants (GDPs), etc.]. |

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(vii) |
A backfit analysis, as defined in the Backfit Rule (10 CFR 50.109 for power reactors or 10 CFR 76.76 for GDPs), unless the proposed action constitutes a compliance or adequate protection backfit.2, 3, 4 The backfit analysis shall document for consideration pertinent available information concerning any of the following factors, as appropriate: |
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(a) |
statement of the specific objectives that the proposed action is intended to achieve |
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(b) |
general description of the activity that the licensee or applicant would be required to perform in order to complete the action |
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(c) |
potential change in the risk to the public from the accidental offsite release of radioactive material |
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(d) |
potential impact on radiological exposure of facility employees and other onsite workers |
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(e) |
installation and continuing costs associated with the action, including the cost of facility downtime or the cost of construction delay |
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(f) |
potential safety impact of changes in plant or operational complexity, including the relationship to proposed and existing regulatory requirements and staff positions |
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(g) |
estimated resource burden on the NRC associated with the proposed action and the availability of such resources |
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(h) |
otential impact of differences in facility type, design, or age on the relevancy and practicality of the proposed action |
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(i) |
whether the proposed action is interim or final, and if interim, the justification for imposing the proposed action on an interim basis |
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(j) |
staff evaluation of comments received as a result of the notice and comment process (for both rulemaking actions and proposed generic correspondence) |
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(k)
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an evaluation that demonstrates how the proposed action should be prioritized and scheduled in light of other ongoing regulatory activities (for each category of nuclear power reactor or nuclear materials facility or activity), which may include any or all of the following information, as appropriate: |
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1. |
proposed priority or schedule |
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2. |
summary of the current backlog of existing requirements awaiting implementation |
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3. |
assessment of whether the implementation of existing requirements should be deferred as a result of the proposed action |
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4. |
any other information that may be considered appropriate with regard to priority, schedule, or cumulative impact (e.g., whether implementation could be delayed pending public comment) |
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(l)
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any other information that is relevant and material to the proposed action |

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(viii) |
The proposing office director's determination (including the rationale for that determination), based on consideration of the previously listed items (i) through (vii), that the following conditions apply: |
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(a) |
The proposed action will yield a substantial increase in the overall protection of public health and safety or the common defense and security. 6, 7 |
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(b) |
The direct and indirect costs of implementation for the affected facilities are justified in view of this increased protection. |
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This requirement applies to proposed backfits that are analyzed in accordance with 10 CFR 50.109(a)(2), 10 CFR 72.62(c), or 10 CFR 76.76(a)(3) (i.e., other than adequate protection or compliance backfits). As a legal matter, the Backfit Rule (10 CFR 50.109) does not apply to nuclear material facilities and activities that are not licensed under 10 CFR Part 50, although footnote 6 does apply to evaluations of proposed backfit actions that affect the selected nuclear facilities and activities. Nonetheless, the staff should consider specific provisions of 10 CFR 72.62 and 10 CFR 76.76, as appropriate, when considering backfit-related matters for independent spent fuel storage installations (ISFSI) and the monitored retrievable storage installations (GDPs), respectively. Additionally, in the context of licensing actions under 10 CFR Part 70, the Commission supported the requirement that "…any new backfit [must] pass a cost-benefit test without the 'substantial increase in safety' test. The Commission believes that modest increases in safety at minimal or inconsequential cost should be justified on a cost-benefit basis."8 |