Information Collection; Indirect Cost Rates, 10861-10862 [2016-04485]

Download as PDF Federal Register / Vol. 81, No. 41 / Wednesday, March 2, 2016 / Notices submission to verify posting (except allow 30 days for posting of comments submitted by mail). Filing Party: Paul M. Keane, Esq., Cichanowicz, Callan, Keane & DeMay, LLP, 50 Main Street, Suite 1045, White Plains, NY 10606. Synopsis: The Agreement authorizes the parties to cooperate and establish a new weekly service in the trade between ports on the U.S. West Coast and ports in China and Japan. DEPARTMENT OF DEFENSE By Order of the Federal Maritime Commission. Dated: February 26, 2016. Rachel E. Dickon, Assistant Secretary. Information Collection; Indirect Cost Rates FEDERAL MINE SAFETY AND HEALTH REVIEW COMMISSION Sunshine Act Notice February 29, 2016. 10:00 a.m., Thursday, March 10, 2016. TIME AND DATE: The Richard V. Backley Hearing Room, Room 511N, 1331 Pennsylvania Avenue NW., Washington, DC 20004 (enter from F Street entrance). PLACE: Open. The Commission will consider and act upon the following in open session: Secretary of Labor v. ICG Illinois, LLC, Docket No. LAKE 2013–160 (Issues include whether the Judge erred in ruling that a violation of the requirement to maintain a refuge alternative was ‘‘significant and substantial.’’) Any person attending this meeting who requires special accessibility features and/or auxiliary aids, such as sign language interpreters, must inform the Commission in advance of those needs. Subject to 29 CFR 2706.150(a)(3) and § 2706.160(d). MATTERS TO BE CONSIDERED: CONTACT PERSON FOR MORE INFORMATION: Emogene Johnson (202) 434–9935/(202) 708–9300 for TDD Relay/1–800–877– 8339 for toll free. mstockstill on DSK4VPTVN1PROD with NOTICES Sarah L. Stewart, Deputy General Counsel. [FR Doc. 2016–04650 Filed 2–29–16; 11:15 am] BILLING CODE 6735–01–P VerDate Sep<11>2014 19:10 Mar 01, 2016 Jkt 238001 [OMB Control No. 9000–0069; Docket 2016– 0053; Sequence 12] Under the provisions of the Paperwork Reduction Act, the Regulatory Secretariat Division will be submitting to the Office of Management and Budget (OMB) a request to review and approve an extension of a previously approved information collection requirement concerning Indirect Cost Rates. DATES: Submit comments on or before May 2, 2016. ADDRESSES: Submit comments identified by Information Collection 9000–0069, Indirect Cost Rates, by any of the following methods: • Regulations.gov: https://www. regulations.gov. Submit comments via the Federal eRulemaking portal by searching the OMB control number. Select the link ‘‘Submit a Comment’’ that corresponds with ‘‘Information Collection 9000– 0069, Indirect Cost Rates’’. Follow the instructions provided at the ‘‘Submit a Comment’’ screen. Please include your name, company name (if any), and ‘‘Information Collection 9000–0069, Indirect Cost Rates’’ on your attached document. • Mail: General Services Administration, Regulatory Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405. ATTN: Ms. Flowers/IC 9000–0069, Indirect Cost Rates. Instructions: Please submit comments only and cite Information Collection 9000–0069, Indirect Cost Rates, in all correspondence related to this collection. Comments received generally will be posted without change to https:// www.regulations.gov, including any personal and/or business confidential information provided. To confirm receipt of your comment(s), please check www.regulations.gov, approximately two to three days after SUMMARY: PO 00000 Frm 00035 Fmt 4703 Sfmt 4703 Mr. Curtis E. Glover, Sr., Procurement Analyst, Contract Policy Division, at 202–501–1448, or via email at curtis.glover@gsa.gov. FOR FURTHER INFORMATION CONTACT: NATIONAL AERONAUTICS AND SPACE ADMINISTRATION Department of Defense (DOD), General Services Administration (GSA), and National Aeronautics and Space Administration (NASA). ACTION: Notice of request for comments regarding an extension to an existing OMB clearance. BILLING CODE 6731–AA–P STATUS: GENERAL SERVICES ADMINISTRATION AGENCY: [FR Doc. 2016–04586 Filed 3–1–16; 8:45 am] 10861 A. Purpose The contractor’s proposal of final indirect cost rates is necessary for the establishment of rates used to reimburse the contractor for the costs of performing under the contract. The supporting cost data are the cost accounting information normally prepared by organizations under sound management and accounting practices. The proposal and supporting data is used by the contracting official and auditor to verify and analyze the indirect costs and to determine the final indirect cost rates or to prepare the Government negotiating position if negotiation of the rates is required under the contract terms. B. Annual Reporting Burden Respondents: 3,000. Responses per Respondent: 1. Annual Responses: 3,000. Hours per Response: 2,188. Total Burden Hours: 6,564,000. C. Public Comments Public comments are particularly invited on: Whether this collection of information is necessary for the proper performance of functions of the FAR, and whether it will have practical utility; whether our estimate of the public burden of this collection of information is accurate, and based on valid assumptions and methodology; ways to enhance the quality, utility, and clarity of the information to be collected; and ways in which we can minimize the burden of the collection of information on those who are to respond, through the use of appropriate technological collection techniques or other forms of information technology. Obtaining Copies of Proposals: Requesters may obtain a copy of the information collection documents from the General Services Administration, Regulatory Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405, telephone 202–501–4755. Please cite OMB Control No. 9000–0069, Indirect Cost Rates, in all correspondence. E:\FR\FM\02MRN1.SGM 02MRN1 10862 Federal Register / Vol. 81, No. 41 / Wednesday, March 2, 2016 / Notices Dated: February 25, 2016. Lorin S. Curit, Director, Federal Acquisition Policy Division, Office of Governmentwide Acquisition Policy, Office of Acquisition Policy, Office of Governmentwide Policy. [FR Doc. 2016–04485 Filed 3–1–16; 8:45 am] BILLING CODE 6820–EP–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Disease, Disability, and Injury Prevention and Control Special Emphasis Panel (SEP): Initial Review The meeting announced below concerns Childhood Obesity Research Demonstration 2.0, FOA DP 16–004, initial review. SUMMARY: This document corrects a notice that was published in the Federal Register on February 10, 2016, Volume 81, Number 27, pages 7123–7124. The meeting time and date should read as follows: Time and Date: 10:00 a.m.–6:00 p.m., EDT, March 15, 2016 (Closed). FOR FURTHER INFORMATION CONTACT: Jaya Raman, Ph.D., Scientific Review Officer, CDC, 4770 Buford Highway NE., Mailstop F80, Atlanta, Georgia 30341, Telephone: (770) 488–6511, KVA5@ cdc.gov. The Director, Management Analysis and Services Office, has been delegated the authority to sign Federal Register notices pertaining to announcements of meetings and other committee management activities, for both the Centers for Disease Control and Prevention and the Agency for Toxic Substances and Disease Registry. Elaine L. Baker, Director, Management Analysis and Services Office, Centers for Disease Control and Prevention. [FR Doc. 2016–04591 Filed 3–1–16; 8:45 am] BILLING CODE 4163–18–P mstockstill on DSK4VPTVN1PROD with NOTICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention Clinical Laboratory Improvement Advisory Committee In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), the Centers for Disease Control and Prevention (CDC) VerDate Sep<11>2014 19:10 Mar 01, 2016 Jkt 238001 announces the following committee meeting. Times And Dates: 8:30 a.m.–5:00 p.m., April 13, 2016; 8:30 a.m.–12:00 p.m., April 14, 2016. Place: CDC, 1600 Clifton Road NE., Tom Harkin Global Communications Center, Building 19, Auditorium B, Atlanta, Georgia 30333. Status: Open to the public, limited only by the space available. The meeting room accommodates approximately 100 people. This meeting will also be webcast, please see information below. Purpose: This Committee is charged with providing scientific and technical advice and guidance to the Secretary of Health and Human Services (HHS); the Assistant Secretary for Health; the Director, Centers for Disease Control and Prevention; the Commissioner, Food and Drug Administration (FDA); and the Administrator, Centers for Medicare and Medicaid Services (CMS). The advice and guidance pertain to general issues related to improvement in clinical laboratory quality and laboratory medicine practice and specific questions related to possible revision of the Clinical Laboratory Improvement Amendment (CLIA) standards. Examples include providing guidance on studies designed to improve safety, effectiveness, efficiency, timeliness, equity, and patientcenteredness of laboratory services; revisions to the standards under which clinical laboratories are regulated; the impact of proposed revisions to the standards on medical and laboratory practice; and the modification of the standards and provision of nonregulatory guidelines to accommodate technological advances, such as new test methods, the electronic transmission of laboratory information, and mechanisms to improve the integration of public health and clinical laboratory practices. Matters For Discussion: The agenda will include agency updates from CDC, CMS, and FDA. Presentations and discussions will include methods for improving the effectiveness/efficiency of CLIAC meetings; an overview of the CMS Advisory Panel on Clinical Diagnostic Laboratory Tests; laboratory interoperability including the Office of the National Coordinator for Health Information Technology (ONC) policies and engagement with clinical laboratories; update on the cytology workload project; update on laboratory biosafety in clinical laboratories; and future CLIAC topics. Agenda items are subject to change as priorities dictate. Webcast: The meeting will also be webcast. Persons interested in viewing PO 00000 Frm 00036 Fmt 4703 Sfmt 4703 the webcast can access information at: https://cdclabtraining.adobeconnect. com/aprilcliac/. In-Person Attendance Online Registration Required: All people attending the CLIAC meeting in-person are required to register for the meeting online at least 5 business days in advance for U.S. citizens and at least 10 business days in advance for international registrants. Register at: https://www.cdc.gov/cliac/Meetings/ MeetingDetails.aspx#. Register by scrolling down and clicking the ‘‘Register for this Meeting’’ button and completing all forms according to the instructions given. Please complete all the required fields before submitting your registration and submit no later than April 7, 2016 for U.S. registrants and March 31, 2016 for international registrants. Providing Oral or Written Comments: It is the policy of CLIAC to accept written public comments and provide a brief period for oral public comments on agenda items whenever possible. Oral Comments: In general, each individual or group requesting to make oral comments will be limited to a total time of five minutes (unless otherwise indicated). Speakers must also submit their comments in writing for inclusion in the meeting’s Summary Report. To assure adequate time is scheduled for public comments, speakers should notify the contact person below at least one week prior to the meeting date. Written Comments: For individuals or groups unable to attend the meeting, CLIAC accepts written comments until the date of the meeting (unless otherwise stated). However, it is requested that comments be submitted at least one week prior to the meeting date so that the comments may be made available to the Committee for their consideration and for public distribution. Written comments, one hard copy with original signature, should be provided to the contact person listed below, and will be included in the meeting’s Summary Report. Availability of Meeting Materials: To support the green initiatives of the federal government, the CLIAC meeting materials will be made available to the Committee and the public in electronic format (PDF) on the internet instead of by printed copy. Check the CLIAC Web site on the day of the meeting for materials: https://wwwn.cdc.gov/cliac/ cliac_meeting_all_documents.aspx. Note: If using a mobile device to access the materials, please verify that the device’s browser is able to download the files from the CDC’s Web site before the meeting. Alternatively, the files can be downloaded to E:\FR\FM\02MRN1.SGM 02MRN1

Agencies

[Federal Register Volume 81, Number 41 (Wednesday, March 2, 2016)]
[Notices]
[Pages 10861-10862]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-04485]


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DEPARTMENT OF DEFENSE

GENERAL SERVICES ADMINISTRATION

NATIONAL AERONAUTICS AND SPACE ADMINISTRATION

[OMB Control No. 9000-0069; Docket 2016-0053; Sequence 12]


Information Collection; Indirect Cost Rates

AGENCY: Department of Defense (DOD), General Services Administration 
(GSA), and National Aeronautics and Space Administration (NASA).

ACTION: Notice of request for comments regarding an extension to an 
existing OMB clearance.

-----------------------------------------------------------------------

SUMMARY: Under the provisions of the Paperwork Reduction Act, the 
Regulatory Secretariat Division will be submitting to the Office of 
Management and Budget (OMB) a request to review and approve an 
extension of a previously approved information collection requirement 
concerning Indirect Cost Rates.

DATES: Submit comments on or before May 2, 2016.

ADDRESSES: Submit comments identified by Information Collection 9000-
0069, Indirect Cost Rates, by any of the following methods:
     Regulations.gov: https://www.regulations.gov.
    Submit comments via the Federal eRulemaking portal by searching the 
OMB control number. Select the link ``Submit a Comment'' that 
corresponds with ``Information Collection 9000-0069, Indirect Cost 
Rates''. Follow the instructions provided at the ``Submit a Comment'' 
screen. Please include your name, company name (if any), and 
``Information Collection 9000-0069, Indirect Cost Rates'' on your 
attached document.
     Mail: General Services Administration, Regulatory 
Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405. 
ATTN: Ms. Flowers/IC 9000-0069, Indirect Cost Rates.
    Instructions: Please submit comments only and cite Information 
Collection 9000-0069, Indirect Cost Rates, in all correspondence 
related to this collection. Comments received generally will be posted 
without change to https:// www.regulations.gov, including any personal 
and/or business confidential information provided. To confirm receipt 
of your comment(s), please check www.regulations.gov, approximately two 
to three days after submission to verify posting (except allow 30 days 
for posting of comments submitted by mail).

FOR FURTHER INFORMATION CONTACT: Mr. Curtis E. Glover, Sr., Procurement 
Analyst, Contract Policy Division, at 202-501-1448, or via email at 
curtis.glover@gsa.gov.

A. Purpose

    The contractor's proposal of final indirect cost rates is necessary 
for the establishment of rates used to reimburse the contractor for the 
costs of performing under the contract. The supporting cost data are 
the cost accounting information normally prepared by organizations 
under sound management and accounting practices.
    The proposal and supporting data is used by the contracting 
official and auditor to verify and analyze the indirect costs and to 
determine the final indirect cost rates or to prepare the Government 
negotiating position if negotiation of the rates is required under the 
contract terms.

B. Annual Reporting Burden

    Respondents: 3,000.
    Responses per Respondent: 1.
    Annual Responses: 3,000.
    Hours per Response: 2,188.
    Total Burden Hours: 6,564,000.

C. Public Comments

    Public comments are particularly invited on: Whether this 
collection of information is necessary for the proper performance of 
functions of the FAR, and whether it will have practical utility; 
whether our estimate of the public burden of this collection of 
information is accurate, and based on valid assumptions and 
methodology; ways to enhance the quality, utility, and clarity of the 
information to be collected; and ways in which we can minimize the 
burden of the collection of information on those who are to respond, 
through the use of appropriate technological collection techniques or 
other forms of information technology.
    Obtaining Copies of Proposals: Requesters may obtain a copy of the 
information collection documents from the General Services 
Administration, Regulatory Secretariat Division (MVCB), 1800 F Street 
NW., Washington, DC 20405, telephone 202-501-4755. Please cite OMB 
Control No. 9000-0069, Indirect Cost Rates, in all correspondence.


[[Page 10862]]


    Dated: February 25, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division, Office of Governmentwide 
Acquisition Policy, Office of Acquisition Policy, Office of 
Governmentwide Policy.
[FR Doc. 2016-04485 Filed 3-1-16; 8:45 am]
 BILLING CODE 6820-EP-P

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