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, “Domestic Licensing of
Production and Utilization Facilities.” 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, “Licenses, Certifications, and Approvals for Nuclear Power
Plants.” 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
Summary’s (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.