Agency Forms Undergoing Paperwork Reduction Act Review, 91-92 [2015-33092]

Download as PDF Federal Register / Vol. 81, No. 1 / Monday, January 4, 2016 / Notices Act of 1956 (12 U.S.C. 1841 et seq.) (BHC Act), Regulation Y (12 CFR part 225), and all other applicable statutes and regulations to become a bank holding company and/or to acquire the assets or the ownership of, control of, or the power to vote shares of a bank or bank holding company and all of the banks and nonbanking companies owned by the bank holding company, including the companies listed below. The applications listed below, as well as other related filings required by the Board, are available for immediate inspection at the Federal Reserve Bank indicated. The applications will also be available for inspection at the offices of the Board of Governors. Interested persons may express their views in writing on the standards enumerated in the BHC Act (12 U.S.C. 1842(c)). If the proposal also involves the acquisition of a nonbanking company, the review also includes whether the acquisition of the nonbanking company complies with the standards in section 4 of the BHC Act (12 U.S.C. 1843). Unless otherwise noted, nonbanking activities will be conducted throughout the United States. Unless otherwise noted, comments regarding each of these applications must be received at the Reserve Bank indicated or the offices of the Board of Governors not later than January 28, 2016. A. Federal Reserve Bank of Richmond (Adam M. Drimer, Assistant Vice President) 701 East Byrd Street, Richmond, Virginia 23261–4528: 1. Capital Bank Financial Corp., Charlotte, North Carolina; to merge with CommunityOne Bancorp, and thereby indirectly acquire CommunityOne Bank, National Association, both in Charlotte, North Carolina. B. Federal Reserve Bank of St. Louis (Yvonne Sparks, Community Development Officer) P.O. Box 442, St. Louis, Missouri 63166–2034: 1. Royal Bancshares, Inc., University City, Missouri; to acquire 100 percent of the voting shares of Frontenac Bancshares, Inc., and thereby indirectly acquire Frontenac Bank, both in Earth City, Missouri. In connection with this application, Royal Acquisition LLC, University City, Missouri, has applied to become a bank holding company by acquiring 100 percent of the voting shares of Frontenac Bank, Earth City, Missouri. DEPARTMENT OF HEALTH AND HUMAN SERVICES Formations of, Acquisitions by, and Mergers of Bank Holding Companies The companies listed in this notice have applied to the Board for approval, pursuant to the Bank Holding Company Board of Governors of the Federal Reserve System, December 29, 2015. Michael J. Lewandowski, Associate Secretary of the Board. [FR Doc. 2015–33017 Filed 12–31–15; 8:45 am] (Autism and Developmental Disabilities Monitoring (ADDM) Network)—New—National Center for Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC). issue a Notice of Schedule for Environmental Review. If a Notice of Schedule for Environmental Review is issued, it will indicate, among other milestones, the anticipated date for the Commission staff’s issuance of the final environmental impact statement (FEIS) or EA for this proposal. The filing of the EA in the Commission’s public record for this proceeding or the issuance of a Notice of Schedule for Environmental Review will serve to notify federal and state agencies of the timing for the completion of all necessary reviews, and the subsequent need to complete all federal authorizations within 90 days of the date of issuance of the Commission staff’s FEIS or EA. Persons who wish to comment only on the environmental review of this project should submit an original and two copies of their comments to the Secretary of the Commission. Environmental commenters will be placed on the Commission’s environmental mailing list, will receive copies of the environmental documents, and will be notified of meetings associated with he Commission’s environmental review process. Environmental commenters will not be required to serve copies of filed documents on all other parties. However, the non-party commenters will not receive copies of all documents filed by other parties or issued by the Commission (except for the mailing of environmental documents issued by the Commission) and will not have the right to seek court review of the Commission’s final order. The Commission strongly encourages electronic filings of comments, protests, and interventions via the internet in lieu of paper. See 18 CFR 385.2001(a) (1) (iii) and the instructions on the Commission’s Web site (www.ferc.gov) under the ‘‘e-Filing’’ link. Persons unable to file electronically should submit an original and five copies of the protest or intervention to the Federal Energy Regulatory Commission, 888 First Street NE., Washington, DC 20426. Dated: December 28, 2015. Nathaniel J. Davis, Sr., Deputy Secretary. [FR Doc. 2015–33033 Filed 12–31–15; 8:45 am] BILLING CODE 6717–01–P tkelley on DSK3SPTVN1PROD with NOTICES 91 FEDERAL RESERVE SYSTEM VerDate Sep<11>2014 16:43 Dec 31, 2015 Jkt 238001 BILLING CODE 6210–01–P PO 00000 Frm 00031 Fmt 4703 Sfmt 4703 Centers for Disease Control and Prevention [30Day–15–2015; Docket No. CDC–2015– 0023] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paper Reduction Act of 1995. The notice for the proposed information collection is published to obtain comments from the public and affected agencies. Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address any of the following: (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404)639–7570 or send an email to omb@cdc.gov. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202)395–5806. Written comments should be received within 30 days of this notice. Proposed Project Performance Measurement and Program Evaluation E:\FR\FM\04JAN1.SGM 04JAN1 92 Federal Register / Vol. 81, No. 1 / Monday, January 4, 2016 / Notices Background and Brief Description In January 2015, CDC launched a new phase of funding for its autism spectrum disorder (ASD) surveillance program through a new cooperative agreement: ‘‘Enhancing Public Health Surveillance of Autism Spectrum Disorder and Other Developmental Disabilities through the Autism and Developmental Disabilities Monitoring (ADDM) Network’’ under the Funding Opportunity Announcement (FOA) DD15–1501. Through this cooperative agreement, funding is provided to enhance tracking at eight existing sites and to launch two new sites. Awards were made to state/ local health departments and/or their designated representatives, including Colorado Department of Public Health and Environment, Johns Hopkins University, Rutgers University, University of Arizona, University of Arkansas for Medical Sciences, University of North Carolina at Chapel Hill, University of Minnesota, University of Wisconsin-Madison, Vanderbilt University, and Washington University in St. Louis. Four sites received funding to carry out Component A, which focuses on surveillance of ASD and either cerebral palsy or intellectual disability among 8year-olds. Six sites received funding to carry out both Component A as well as Component B, which focuses on surveillance of ASD among 4-year-olds. In addition to the sites funded under the cooperative agreement, CDC also administers a site in Atlanta, Georgia, commonly known as the Metropolitan Atlanta Developmental Disabilities Surveillance Program (MADDSP). CDC seeks to request OMB approval to collect performance monitoring and program evaluation information from all sites participating in the Autism and Developmental Disabilities Monitoring Network (including the site administered by CDC). Over the course of the four-year funding cycle, each site will provide feedback via site-specific interviews, a Checklist, Worksheets, and Performance Measures at six month and two-year intervals. The interviews will occur on pre-established individual site calls that CDC conducts monthly with each grantee. The Worksheets and Performance Measures will be submitted to CDC by completing a Microsoft Excel-based data collection tool and emailing the information to a designated CDC contact. By conducting brief telephone interviews and developing a user-friendly data collection tool in Microsoft Excel, CDC anticipates that the reporting and tracking burden for awardees will be reduced due to: (1) Use of preestablished meeting time to conduct interviews, (2) awardees’ familiarity with the software, which reduces training burden; and (3) the compatibility of the templates with other record keeping processes that are already in place for many awardees. CDC staff and contractors will be responsible for converting each awardee’s submissions into a secure Microsoft Excel spreadsheet for reporting and analysis. CDC anticipates that respondent burden will be slightly higher at the initial six-month submission and will also be slightly higher for sites completing Component A&B compared to just Component A. The information to be collected will help CDC and awardees assure compliance with cooperative agreement requirements, support program evaluation efforts, and obtain information needed to respond to inquiries about program activities and program impact from Congress and other stakeholders. OMB approval is requested for three years. Participation is required as a condition of cooperative agreement funding. There are no costs to respondents other than their time. The total estimated burden hours are 122. ESTIMATED ANNUALIZED BURDEN HOURS Form name Component A only (initial six-month submission) ................... Interview ................................. Worksheets ............................ Performance Measure ............ Interview ................................. Worksheets ............................ Performance Measures .......... Interview ................................. Worksheets ............................ Performance Measures .......... Interview ................................. Worksheets ............................ Performance Measures .......... Component A&B (initial six-month submission) ...................... Component A only (subsequent six-month and two-year submissions). Component A&B (subsequent six-month and two-year submissions). Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. tkelley on DSK3SPTVN1PROD with NOTICES [FR Doc. 2015–33092 Filed 12–31–15; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–359/360] Agency Information Collection Activities: Proposed Collection; Comment Request BILLING CODE 4163–18–P Centers for Medicare & Medicaid Services. ACTION: Notice. AGENCY: VerDate Sep<11>2014 16:43 Dec 31, 2015 Jkt 238001 PO 00000 Frm 00032 Fmt 4703 Sfmt 4703 Number of responses per respondent Number of respondents Type of respondents 5 5 5 6 6 6 5 5 5 6 6 6 1 1 1 1 1 1 5 5 5 5 5 5 Average burden per response (in hours) 3/60 90/60 30/60 3/60 120/60 42/60 3/60 60/60 18/60 3/60 90/60 30/60 The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS’ intention to collect information from the public. Under the Paperwork Reduction Act of 1995 (the PRA), federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information (including each proposed extension or reinstatement of an existing collection of information) and to allow 60 days for public comment on the proposed action. Interested persons are SUMMARY: E:\FR\FM\04JAN1.SGM 04JAN1

Agencies

[Federal Register Volume 81, Number 1 (Monday, January 4, 2016)]
[Notices]
[Pages 91-92]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-33092]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-15-2015; Docket No. CDC-2015-0023]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) has submitted 
the following information collection request to the Office of 
Management and Budget (OMB) for review and approval in accordance with 
the Paper Reduction Act of 1995. The notice for the proposed 
information collection is published to obtain comments from the public 
and affected agencies.
    Written comments and suggestions from the public and affected 
agencies concerning the proposed collection of information are 
encouraged. Your comments should address any of the following: (a) 
Evaluate whether the proposed collection of information is necessary 
for the proper performance of the functions of the agency, including 
whether the information will have practical utility; (b) Evaluate the 
accuracy of the agency's estimate of the burden of the proposed 
collection of information, including the validity of the methodology 
and information to be collected; (d) Minimize the burden of the 
collection of information on those who are to respond, including 
through the use of appropriate automated, electronic, mechanical, or 
other technological collection techniques or other forms of information 
technology, e.g., permitting electronic submission of responses; and 
(e) Assess information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404)639-7570 or send an email to omb@cdc.gov. Direct written comments 
and/or suggestions regarding the items contained in this notice to the 
Attention: CDC Desk Officer, Office of Management and Budget, 
Washington, DC 20503 or by fax to (202)395-5806. Written comments 
should be received within 30 days of this notice.

Proposed Project

Performance Measurement and Program Evaluation

    (Autism and Developmental Disabilities Monitoring (ADDM) Network)--
New--National Center for Birth Defects and Developmental Disabilities 
(NCBDDD), Centers for Disease Control and Prevention (CDC).

[[Page 92]]

Background and Brief Description
    In January 2015, CDC launched a new phase of funding for its autism 
spectrum disorder (ASD) surveillance program through a new cooperative 
agreement: ``Enhancing Public Health Surveillance of Autism Spectrum 
Disorder and Other Developmental Disabilities through the Autism and 
Developmental Disabilities Monitoring (ADDM) Network'' under the 
Funding Opportunity Announcement (FOA) DD15-1501. Through this 
cooperative agreement, funding is provided to enhance tracking at eight 
existing sites and to launch two new sites. Awards were made to state/
local health departments and/or their designated representatives, 
including Colorado Department of Public Health and Environment, Johns 
Hopkins University, Rutgers University, University of Arizona, 
University of Arkansas for Medical Sciences, University of North 
Carolina at Chapel Hill, University of Minnesota, University of 
Wisconsin-Madison, Vanderbilt University, and Washington University in 
St. Louis. Four sites received funding to carry out Component A, which 
focuses on surveillance of ASD and either cerebral palsy or 
intellectual disability among 8-year-olds. Six sites received funding 
to carry out both Component A as well as Component B, which focuses on 
surveillance of ASD among 4-year-olds. In addition to the sites funded 
under the cooperative agreement, CDC also administers a site in 
Atlanta, Georgia, commonly known as the Metropolitan Atlanta 
Developmental Disabilities Surveillance Program (MADDSP).
    CDC seeks to request OMB approval to collect performance monitoring 
and program evaluation information from all sites participating in the 
Autism and Developmental Disabilities Monitoring Network (including the 
site administered by CDC). Over the course of the four-year funding 
cycle, each site will provide feedback via site-specific interviews, a 
Checklist, Worksheets, and Performance Measures at six month and two-
year intervals. The interviews will occur on pre-established individual 
site calls that CDC conducts monthly with each grantee. The Worksheets 
and Performance Measures will be submitted to CDC by completing a 
Microsoft Excel-based data collection tool and emailing the information 
to a designated CDC contact. By conducting brief telephone interviews 
and developing a user-friendly data collection tool in Microsoft Excel, 
CDC anticipates that the reporting and tracking burden for awardees 
will be reduced due to: (1) Use of pre-established meeting time to 
conduct interviews, (2) awardees' familiarity with the software, which 
reduces training burden; and (3) the compatibility of the templates 
with other record keeping processes that are already in place for many 
awardees. CDC staff and contractors will be responsible for converting 
each awardee's submissions into a secure Microsoft Excel spreadsheet 
for reporting and analysis. CDC anticipates that respondent burden will 
be slightly higher at the initial six-month submission and will also be 
slightly higher for sites completing Component A&B compared to just 
Component A.
    The information to be collected will help CDC and awardees assure 
compliance with cooperative agreement requirements, support program 
evaluation efforts, and obtain information needed to respond to 
inquiries about program activities and program impact from Congress and 
other stakeholders.
    OMB approval is requested for three years. Participation is 
required as a condition of cooperative agreement funding. There are no 
costs to respondents other than their time. The total estimated burden 
hours are 122.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                                      Average
                                                                     Number of       Number of      burden per
          Type of respondents                   Form name           respondents    responses per   response  (in
                                                                                    respondent        hours)
----------------------------------------------------------------------------------------------------------------
Component A only (initial six-month     Interview...............               5               1            3/60
 submission).                           Worksheets..............               5               1           90/60
                                        Performance Measure.....               5               1           30/60
Component A&B (initial six-month        Interview...............               6               1            3/60
 submission).                           Worksheets..............               6               1          120/60
                                        Performance Measures....               6               1           42/60
Component A only (subsequent six-month  Interview...............               5               5            3/60
 and two-year submissions).             Worksheets..............               5               5           60/60
                                        Performance Measures....               5               5           18/60
Component A&B (subsequent six-month     Interview...............               6               5            3/60
 and two-year submissions).             Worksheets..............               6               5           90/60
                                        Performance Measures....               6               5           30/60
----------------------------------------------------------------------------------------------------------------


Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific 
Integrity, Office of the Associate Director for Science, Office of the 
Director, Centers for Disease Control and Prevention.
[FR Doc. 2015-33092 Filed 12-31-15; 8:45 am]
 BILLING CODE 4163-18-P