81 FR 6519 - Submission for OMB Review; Evaluation of Export Offers

DEPARTMENT OF DEFENSE
GENERAL SERVICES ADMINISTRATION
NATIONAL AERONAUTICS AND SPACE ADMINISTRATION

Federal Register Volume 81, Issue 25 (February 8, 2016)

Page Range		6519-6520
FR Document		2016-02448

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 ``Information Collection 9000-0057, Evaluation of Export Offers.'' A notice was published in the Federal Register at 80 FR 65761 on October 27, 2015. No comments were received.

Federal Register, Volume 81 Issue 25 (Monday, February 8, 2016)

[Federal Register Volume 81, Number 25 (Monday, February 8, 2016)]
[Notices]
[Pages 6519-6520]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2016-02448]


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DEPARTMENT OF DEFENSE

GENERAL SERVICES ADMINISTRATION

NATIONAL AERONAUTICS AND SPACE ADMINISTRATION

[OMB Control No. 9000-0057; Docket 2015-0055; Sequence 24]


Submission for OMB Review; Evaluation of Export Offers

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

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

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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 ``Information Collection 9000-0057, Evaluation of Export 
Offers.'' A notice was published in the Federal Register at 80 FR 65761 
on October 27, 2015. No comments were received.

DATES: Submit comments on or before March 9, 2016.

ADDRESSES: Submit comments regarding this burden estimate or any other 
aspect of this collection of information, including suggestions for 
reducing this burden to: Office of Information and Regulatory Affairs 
of OMB, Attention: Desk Officer for GSA, Room 10236, NEOB, Washington, 
DC 20503. Additionally submit a copy to GSA by any of the following 
methods:
     Regulations.gov: http://www.regulations.gov. Submit 
comments via the Federal eRulemaking portal by inputting ``Information 
Collection 9000-0057, Evaluation of Export Offers'' under the heading 
``Enter Keyword or ID'' and selecting ``Search''. Select the link 
``Submit a Comment'' that corresponds with ``Information Collection 
9000-0057, Evaluation of Export Offers''. Follow the instructions 
provided at the ``Submit a Comment'' screen. Please include your name, 
company name (if any), and ``Information Collection 9000-0057, 
Evaluation of Export Offers'' on your attached document.
     Mail: General Services Administration, Regulatory 
Secretariat Division (MVCB), 1800 F Street NW., Washington, DC 20405. 
ATTN: Ms. Flowers/IC 9000-0057, Evaluation of Export Offers.
    Instructions: Please submit comments only and cite Information 
Collection ``Information Collection 9000-0057, Evaluation of Export 
Offers'' in all correspondence related to this collection. Comments 
received generally will be posted without change to http://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, Office of Governmentwide Acquisition Policy, GSA, 202-501-4082 
or via email at [email protected].

SUPPLEMENTARY INFORMATION: 

A. Purpose

    Offers submitted in response to Government solicitations must be 
evaluated and awards made on the basis of the lowest laid down cost to 
the Government at the overseas port of discharge, via methods and ports 
compatible with required delivery dates and conditions affecting 
transportation know at the time of evaluation. FAR provision 52.247-51, 
``Evaluation of Export Offers,'' is required for insertion in 
Government solicitations when supplies are to be exported through 
Contiguous United States (CONUS) ports and offers are solicited on a 
free onboard (f.o.b.) origin or f.o.b. destination basis. The provision 
has three alternates, to be used (1) when the CONUS ports of export are 
DoD water terminals, (2) when offers are solicited on an f.o.b. origin 
only basis, and (3) when offers are solicited on an f.o.b. destination 
only basis. The provision

[[Page 6520]]

collects information regarding the vendor's preference for delivery 
ports. The information is used to evaluate offers [on the basis of 
shipment through the port resulting in the lowest cost to the 
Government.

B. Annual Reporting Burden

    Respondents: 100.
    Responses per Respondent: 4.
    Annual Responses: 400.
    Hours per Response: 0.25.
    Total Burden Hours: 100.

C. Public Comments

    Public comments are particularly invited on: Whether this 
collection of information is necessary; 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 Number ``9000-0057, Evaluation of Export Offers'' in all 
correspondence.

    Dated: February 3, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy Division, Office of Governmentwide 
Acquisition Policy, Office of Acquisition Policy, Office of 
Governmentwide Policy.
[FR Doc. 2016-02448 Filed 2-5-16; 8:45 am]
BILLING CODE 6820-EP-P

6520 Federal Register / Vol. 81, No. 25 / Monday, February 8, 2016 / Notices

collects information regarding the (42 U.S.C. 300aa–26), the Centers for period, and in consultation with the
vendor’s preference for delivery ports. Disease Control and Prevention (CDC) Advisory Commission on Childhood
The information is used to evaluate within the Department of Health and Vaccines, appropriate health care
offers [on the basis of shipment through Human Services (HHS) develops provider and parent organizations, and
the port resulting in the lowest cost to vaccine information materials that all the Food and Drug Administration. The
the Government. health care providers are required to law also requires that the information
give to patients/parents prior to contained in the materials be based on
B. Annual Reporting Burden administration of specific vaccines. available data and information, be
Respondents: 100. HHS/CDC seeks written comment on the presented in understandable terms, and
Responses per Respondent: 4. proposed updated vaccine information include:
Annual Responses: 400. statements for hepatitis A and hepatitis (1) A concise description of the
Hours per Response: 0.25. B vaccines. benefits of the vaccine,
Total Burden Hours: 100.
DATES: Written comments must be (2) A concise description of the risks
C. Public Comments received on or before April 8, 2016. associated with the vaccine,
Public comments are particularly ADDRESSES: You may submit comments, (3) A statement of the availability of
invited on: Whether this collection of identified by Docket No. CDC–2016– the National Vaccine Injury
information is necessary; whether it will 0015, by any of the following methods: Compensation Program, and
have practical utility; whether our • Federal eRulemaking Portal: http:// (4) Such other relevant information as
estimate of the public burden of this www.regulations.gov. Follow the may be determined by the Secretary.
collection of information is accurate, instructions for submitting comments. The vaccines initially covered under
• Mail: Written comments should be the National Vaccine Injury
and based on valid assumptions and
addressed to Suzanne Johnson-DeLeon, Compensation Program were diphtheria,
methodology; ways to enhance the
National Center for Immunization and tetanus, pertussis, measles, mumps,
quality, utility, and clarity of the
Respiratory Diseases, Centers for rubella and poliomyelitis vaccines.
information to be collected; and ways in
Disease Control and Prevention, Since April 15, 1992, any health care
which we can minimize the burden of
Mailstop A–19, 1600 Clifton Road NE., provider in the United States who
the collection of information on those
Atlanta, Georgia 30329. intends to administer one of these
who are to respond, through the use of
Instructions: All submissions received covered vaccines is required to provide
appropriate technological collection
must include the agency name and copies of the relevant vaccine
techniques or other forms of information
docket number. All relevant comments information materials prior to
technology.
received will be posted without change administration of any of these vaccines.
Obtaining Copies of Proposals:
to http://regulations.gov, including any Since then, the following vaccines have
Requesters may obtain a copy of the
personal information provided. For been added to the National Vaccine
information collection documents from
access to the docket to read background Injury Compensation Program, requiring
the General Services Administration,
documents or comments received, go to use of vaccine information materials for
Regulatory Secretariat Division (MVCB),
http://www.regulations.gov. them as well: Hepatitis B, Haemophilus
1800 F Street NW., Washington, DC
20405, telephone 202–501–4755. Please FOR FURTHER INFORMATION CONTACT: Skip influenzae type b (Hib), varicella
cite OMB Control Number ‘‘9000–0057, Wolfe (crw4@cdc.gov), National Center (chickenpox), pneumococcal conjugate,
Evaluation of Export Offers’’ in all for Immunization and Respiratory rotavirus, hepatitis A, meningococcal,
correspondence. Diseases, Centers for Disease Control human papillomavirus (HPV), and
and Prevention, Mailstop A–19, 1600 seasonal influenza vaccines.
Dated: February 3, 2016. Clifton Road NE., Atlanta, Georgia Instructions for use of the vaccine
Lorin S. Curit, 30329. information materials are found on the
Director, Federal Acquisition Policy Division, CDC Web site at: http://www.cdc.gov/
SUPPLEMENTARY INFORMATION: The
Office of Governmentwide Acquisition Policy,
National Childhood Vaccine Injury Act vaccines/hcp/vis/index.html.
Office of Acquisition Policy, Office of
Governmentwide Policy. of 1986 (Pub. L. 99–660), as amended by HHS/CDC is proposing updated
section 708 of Public Law 103–183, versions of the hepatitis A and hepatitis
[FR Doc. 2016–02448 Filed 2–5–16; 8:45 am]
added section 2126 to the Public Health B vaccine information statements.
BILLING CODE 6820–EP–P
Service Act. Section 2126, codified at 42 The vaccine information materials
U.S.C. 300aa–26, requires the Secretary referenced in this notice are being
of Health and Human Services to developed in consultation with the
DEPARTMENT OF HEALTH AND Advisory Commission on Childhood
develop and disseminate vaccine
HUMAN SERVICES Vaccines, the Food and Drug
information materials for distribution by
Centers for Disease Control and all health care providers in the United Administration, and parent and health
Prevention States to any patient (or to the parent or care provider groups.
legal representative in the case of a We invite written comment on the
[Docket No. CDC–2016–0015] child) receiving vaccines covered under proposed revised vaccine information
the National Vaccine Injury materials entitled ‘‘Hepatitis A Vaccine:
Proposed Revised Vaccine Information Compensation Program (VICP). What You Need to Know’’ and
Materials for Hepatitis A and Hepatitis Development and revision of the ‘‘Hepatitis B Vaccine: What You Need to
asabaliauskas on DSK5VPTVN1PROD with NOTICES

B Vaccines vaccine information materials, also Know.’’ Copies of the proposed vaccine
AGENCY: Centers for Disease Control and known as Vaccine Information information materials are available at
Prevention (CDC), Department of Health Statements (VIS), have been delegated http://www.regulations.gov (see Docket
and Human Services (HHS). by the Secretary to the Centers for Number CDC–2016–0015). Comments
ACTION: Notice with comment period. Disease Control and Prevention (CDC). submitted will be considered in
Section 2126 requires that the materials finalizing these materials. When the
SUMMARY: Under the National be developed, or revised, after notice to final materials are published in the
Childhood Vaccine Injury Act (NCVIA) the public, with a 60-day comment Federal Register, the notice will include

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Document Created: 2016-02-06 00:24:07
Document Modified: 2016-02-06 00:24:07

Category		Regulatory Information
Collection		Federal Register
sudoc Class		AE 2.7: GS 4.107: AE 2.106:
Publisher		Office of the Federal Register, National Archives and Records Administration
Section		Notices
Action		Notice of request for public comments regarding an extension to an existing OMB clearance.
Dates		Submit comments on or before March 9, 2016.
Contact		Mr. Curtis E. Glover, Sr., Procurement Analyst, Office of Governmentwide Acquisition Policy, GSA, 202-501-4082 or via email at [email protected]
FR Citation		81 FR 6519

81 FR 6519 - Submission for OMB Review; Evaluation of Export Offers

DEPARTMENT OF DEFENSEGENERAL SERVICES ADMINISTRATIONNATIONAL AERONAUTICS AND SPACE ADMINISTRATION

Federal Register Volume 81, Issue 25 (February 8, 2016)

DEPARTMENT OF DEFENSE
GENERAL SERVICES ADMINISTRATION
NATIONAL AERONAUTICS AND SPACE ADMINISTRATION