Voluntary Reporting of Planned New Reactor Applications
Revision of a currently approved collection
No
Regular
12/30/2024
Requested
Previously Approved
36 Months From Approved
01/31/2025
20
20
1,405
610
0
0
This voluntary information collection assists the NRC in determining resource and budget needs as well as aligning the proper allocation and utilization of resources to support applicant submittals, future construction-related activities, and other anticipated Part 50 and/or Part 52 of Title 10 of the Code of Federal Regulations (10 CFR) licensing and design certification rulemaking actions. In addition, information provided to the NRC staff is intended to promote early communications between the NRC and the respective addressees about potential 10 CFR Part 50 and/or Part 52 licensing actions and related activities, submission dates, and plans for construction and inspection activities. The overarching goal of this information collection is to assist the NRC staff more effectively and efficiently plan, schedule, and implement activities and reviews in a timely manner.
There has been an increase in the cost of the hourly rate from $279/hr. to $300/hr. for this cycle.
The RIS is targeting a wider audience from previous versions of this RIS. The addresses are all holders of, applicants for, or potential applicants for a CP or LWA for a power reactor or nonpower production and utilization facility, or applicants or potential applicants for an OL for a power reactor or nonpower production and utilization facility under Title 10 of the Code of Federal Regulations (10 CFR) Part 50, âDomestic Licensing of Production and Utilization Facilities.â All holders of, applicants for, or potential applicants for an ESP, standard DC, SDA, or ML, or applicants or potential applicants for a COL under 10 CFR Part 52, âLicenses, Certifications, and Approvals for Nuclear Power Plants.â The purpose of the wider audience is to ensure all applicants and potential applicants are able to inform the NRC of potential applications or regulatory engagements.
External programs are contributing to the progression of advanced reactor designs, causing an influx of applications during this clearance cycle. Due to these programs, ongoing robust pre-application engagements (i.e., topical report reviews), responses to Regulatory Information Summaryâs (RIS), Regulatory Engagement Plans (REPs), and meetings, discussions and continuous contact with prospective stakeholders, the agency is expected to receive applications for, CP, ESP, SDAs and certifications, MLs, COLs, for commercial nuclear power reactors, as well as OLs related to the licensing processes that apply to LWR and non-light water reactors (NLWR). The effects of these projected applications are as follows:
The total burden this cycle increased from 610 to 1405 hours, an increase of 795 hours. Additionally, the number of respondents has increased from 10 in the previous cycle to 20 with the anticipated submission of regulatory engagement plans.
The NRC would like to obtain information related to technical and licensing process and anticipated schedules related to an applicant submission. The purpose of this is to ensure the NRC is able to budget and allocate appropriate resources for the anticipated applications. In addition to answering the RIS questions, applications or potential applicants may submit a Regulatory Engagement Plan to inform the NRC of their intent to submit an application and/or engage in preapplication activities.
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.