Proposed Information Collection; Comment Request; Survey: Expenditures Incurred by Recipients of Biomedical Research and Development Awards From the National Institutes of Health (NIH), 28672-28674 [2014-11453]
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28672
Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices
SUPPLEMENTARY INFORMATION:
Background
On October 2, 2013, the Helium
Stewardship Act of 2013 (Pub. L. 113–
40) reauthorized the Act. The purpose of
the RAC is to improve collaborative
relationships among the people that use
and care for the National Forests and to
provide advice and recommendations to
the Forest Service concerning projects
and funding consistent with Title II of
the Act. The duties of the RAC include
monitoring projects, advising the
Secretary on the progress and results of
the monitoring efforts, and making
recommendations to the Forest Service
for any appropriate changes or
adjustments to the projects being
monitored by the RACs.
mstockstill on DSK4VPTVN1PROD with NOTICES
RAC Membership
The RAC will be comprised of 15
members approved by the Secretary of
Agriculture. RAC membership will be
fairly balanced in terms of the points of
view represented and functions to be
performed. The RAC members will
serve 4-year terms. The RAC shall
include representation from the
following interest areas:
(1) Five persons who represent:
(a) Organized Labor or Non-Timber
Forest Product Harvester Groups
(b) Developed Outdoor Recreation,
Off-Highway Vehicle Users, or
Commercial Recreation Activities,
(c) Energy and Mineral Development,
or Commercial or Recreational Fishing
Groups,
(d) Commercial Timber Industry, or
(e) Federal Grazing Permit or Other
Land Use Permit Holders, or
Representative of Non-Industrial Private
Forest Land Owners, within the area for
which the committee is organized.
(2) Five persons who represent:
(a) Nationally or Regionally
Recognized Environmental
Organizations,
(b) Regionally or Locally Recognized
Environmental Organizations,
(c) Dispersed Recreational Activities,
(d) Archaeology and History, or
(e) Nationally or Regionally
Recognized Wild Horse and Burro
Interest, Wildlife Hunting
Organizaitons, or Watershed
Associations.
(3) Five persons who represent:
(a) Hold State-Elected Office,
(b) Hold County or Local-Elected
Office,
(c) American Indian Tribes within or
adjacent to the area for which the
committee is organized,
(d) Area School Officials or Teachers,
or
(e) Affected Public at Large.
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In the event that a vacancy arises, the
Designated Federal Officer may fill the
vacancy with a replacement member
appointed by the Secretary, if an
appropriate replacement member is
available.
Nominations and Applications
Information
The appointment of members to the
RAC will be made by the Secretary of
Agriculture.
Any individual or organization may
nominate one or more qualified persons
to represent the interest areas listed
above. To be considered for
membership, nominees must:
1. Be a resident of Utah,
2. Identify what interest group they
would represent and how they are
qualified to represent that interest
group,
3. State why they want to serve on the
RAC and what they can contribute,
4. Show their past experience in
working successfully as part of a
working group on forest management
activities, and
5. Complete Form AD–755, Advisory
Committee or Research and Promotion
Background Information.
You may contact the person listed
above or retrieve the Form AD–755 from
the following Web site:
www.fs.usda.gov/uwcnf. All
nominations will be vetted by the
Agency.
Equal opportunity practices, in line
with the USDA policies, will be
followed in all appointments to the
RACs. To ensure that the
recommendations of the RACs have
taken into account the needs of the
diverse groups served by the
Department, membership should
include, to the extent practicable,
individuals with demonstrated ability to
represent the needs of all racial and
ethnic groups, women and men, and
persons with disabilities.
Dated: May 13, 2014.
Gregory Parham,
Assistant Secretary of Administration.
[FR Doc. 2014–11548 Filed 5–16–14; 8:45 am]
BILLING CODE 3410–15–P
COMMISSION ON CIVIL RIGHTS
Agenda and Notice of Public Meeting
of the Massachusetts Advisory
Committee
Notice is hereby given, pursuant to
the provisions of the rules and
regulations of the U.S. Commission on
Civil Rights (Commission), and the
Federal Advisory Committee Act
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(FACA), that a briefing meeting of the
Massachusetts Advisory Committee to
the Commission will convene at 10:00
a.m. (EST) on Wednesday, June 11,
2014, at Harvard University Law School,
Lewis Hall, 214B, 1557 Massachusetts
Avenue, Cambridge, MA 02138. The
purpose of the briefing meeting is to
hear from government officials,
advocates, and other experts on the
issue of school discipline in
Massachusetts.
Members of the public are entitled to
submit written comments. The
comments must be received in the
regional office by Friday, July 11, 2014.
Comments may be mailed to the Eastern
Regional Office, U.S. Commission on
Civil Rights, 1331 Pennsylvania
Avenue, Suite 1150, Washington, DC
20425, faxed to (202) 376–7548, or
emailed to Melanie Reingardt at
ero@usccr.gov. Persons who desire
additional information may contact the
Eastern Regional Office at 202–376–
7533.
Persons needing accessibility services
should contact the Eastern Regional
Office at least 10 working days before
the scheduled date of the meeting.
Records generated from this meeting
may be inspected and reproduced at the
Eastern Regional Office, as they become
available, both before and after the
meeting. Persons interested in the work
of this advisory committee are advised
to go to the Commission’s Web site,
www.usccr.gov, or to contact the Eastern
Regional Office at the above phone
number, email, or street address.
The meeting will be conducted
pursuant to the provisions of the rules
and regulations of the Commission and
FACA.
Dated: May 14, 2014.
David Mussatt,
Acting Chief, Regional Programs
Coordination Unit.
[FR Doc. 2014–11503 Filed 5–16–14; 8:45 am]
BILLING CODE 6335–01–P
DEPARTMENT OF COMMERCE
Bureau of Economic Analysis
Proposed Information Collection;
Comment Request; Survey:
Expenditures Incurred by Recipients of
Biomedical Research and
Development Awards From the
National Institutes of Health (NIH)
ACTION:
Notice.
The Department of
Commerce, as part of its continuing
effort to reduce paperwork and
respondent burden, invites the general
SUMMARY:
E:\FR\FM\19MYN1.SGM
19MYN1
Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices
mstockstill on DSK4VPTVN1PROD with NOTICES
public and other Federal agencies to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995, Public Law 104–13 (44
U.S.C. 3506(c)(2)(A)).
DATES: Written comments must be
submitted on or before July 18, 2014.
ADDRESSES: Direct all written comments
to Jennifer Jessup, Departmental
Paperwork Clearance Officer,
Department of Commerce, Room 6616,
14th and Constitution Avenue NW.,
Washington, DC 20230, or via email at
jjessup@doc.gov.
FOR FURTHER INFORMATION CONTACT:
Jennifer A. Bennett, Chief, Government
Fixed Assets Branch, Government
Division (BE–57), Bureau of Economic
Analysis, U.S. Department of
Commerce, Washington, DC 20230;
phone: (202) 606–9769; fax: (202) 606–
5369; or via email at jennifer.bennett@
bea.gov.
SUPPLEMENTARY INFORMATION:
I. Abstract
The survey obtains the distribution of
expenditures incurred by recipients of
biomedical research awards from the
National Institutes of Health (NIH) and
will provide information on how the
NIH award amounts are expended
across several major categories. This
information, along with wage and price
data from other published sources, will
be used to generate the Biomedical
Research and Development Price Index
(BRDPI). BEA develops this index for
NIH under a reimbursable contract. The
BRDPI is an index of prices paid for the
labor, supplies, equipment, and other
inputs required to perform the
biomedical research the NIH supports in
its intramural laboratories and through
its awards to extramural organizations.
The BRDPI is a vital tool for planning
the NIH research budget and analyzing
future NIH programs. A survey of award
recipients is currently the only means
for updating the expenditure category
weights that are used to prepare the
BRDPI.
The proposed survey change revises
the instructions to clarify that
respondent’s should report not only
expenditures from direct NIH award
amounts, but also from NIH awards
received as a sub-recipient from another
institution.
This survey will be voluntary. The
authority for NIH to collect information
for the BRDPI is provided in 45 CFR
subpart C, Post-Award Requirements,
§ 74.21. This sets forth explicit
standards for grantees in establishing
and maintaining financial management
systems and records, and § 74.53 which
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17:17 May 16, 2014
Jkt 232001
provides for the retention of such
records as well as NIH access to such
records.
BEA will administer the survey and
analyze the survey results on behalf of
NIH, through an interagency agreement
between the two agencies. The authority
for the NIH to contract with DOC to
make this collection is the Economy Act
(31 U.S.C. 1535 and 1536).
The ‘‘Special Studies’’ authority, 15
U.S.C. 1525 (first paragraph), permits
DOC to provide, upon the request of any
person, firm, or public or private
organization (a) Special studies on
matters within the authority of the
Department of Commerce, including
preparing from its records special
compilations, lists, bulletins, or reports,
and (b) furnishing transcripts or copies
of its studies, compilations and other
records. NIH’s support for this research
is consistent with the Agency’s duties
and authority under 42 U.S.C. 282.
The information provided by the
respondents will be held confidential
and be used for exclusively statistical
purposes. This pledge of confidentiality
is made under the Confidential
Information Protection provisions of
title V, subtitle A, Public Law 107–347.
Title V is the Confidential Information
Protection and Statistical Efficiency Act
of 2002 (CIPSEA). Section 512 (on
Limitations on Use and Disclosure of
Data and Information) of the Act,
provides that ‘‘data or information
acquired by an agency under a pledge of
confidentiality and for exclusively
statistical purposes shall be used by
officers, employees, or agents of the
agency exclusively for statistical
purposes. Data or information acquired
by an agency under a pledge of
confidentiality for exclusively statistical
purposes shall not be disclosed by an
agency in identifiable form, for any use
other than an exclusively statistical
purpose, except with the informed
consent of the respondent.’’
Responses will be kept confidential
and will not be disclosed in identifiable
form to anyone, other than employees or
agents of BEA or agents of NIH, without
prior written permission of the person
filing the report. By law, each employee
as well as each agent is subject to a jail
term of up to 5 years, a fine of up to
$250,000, or both for disclosing to the
public any identifiable information that
is reported about a business or
institution.
Section 515 of the Information
Quality Guidelines applies to this
survey. The collection and use of this
information complies with all
applicable information quality
guidelines, i.e., those of the Office of
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Fmt 4703
Sfmt 4703
28673
Management and Budget, Department of
Commerce, and BEA.
II. Method of Collection
A survey with a cover letter that
includes a brief description of, and
rationale for, the survey will be sent by
email to potential respondents by the
first week of October in 2014 and by
August of 2015 and 2016. A report of
the respondent’s expenditures of the
NIH award amounts, including NIH
awards received as a sub-recipient from
another institution, following the
proposed format for expenditure
categories included with the survey
form, will be requested to be completed
and submitted online no later than
December 8, which in most years will be
approximately 120 days after mailing.
Survey respondents will be selected on
the basis of award levels, which
determine the weight of the respondent
in the biomedical research and
development price index. Potential
respondents will include (1) The top
100 organizations in total awards, which
account for about 73 percent of total
awards; (2) 40 additional organizations
that are not primarily in the ‘‘Research
and Development (R&D) contracts’’
category; and (3) 10 additional
organizations that are primarily in the
‘‘R&D contracts’’ category.
III. Data
OMB Control Number: 0608–0069.
Form Number: None.
Type of Review: Regular submission.
Affected Public: Universities or other
organizations that are NIH award
recipients.
Estimated Number of Respondents:
120.
Estimated Time per Response: 16
hours, but may vary among respondents
because of differences in institution
structure, size, and complexity.
Estimated Total Annual Burden
Hours: 1,920 hours.
Estimated Total Annual Cost to
Public: $0.
IV. Request for Comments
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the NIH, including
whether the information has practical
utility; (b) the accuracy of the agency’s
estimate of the burden (including hours
and cost) of the proposed collection of
information; (c) ways to enhance the
quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
E:\FR\FM\19MYN1.SGM
19MYN1
28674
Federal Register / Vol. 79, No. 96 / Monday, May 19, 2014 / Notices
of automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and/or
included in the request for OMB
approval of this information collection;
they also will become a matter of public
record.
Dated: May 13, 2014.
Glenna Mickelson,
Management Analyst, Office of Chief
Information Officer.
[FR Doc. 2014–11453 Filed 5–16–14; 8:45 am]
BILLING CODE 3510–EA–P
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–3–2014]
Foreign-Trade Zone 49—Newark, New
Jersey Area; Authorization of
Production Activity; Western Carriers,
Inc. (Kitting of Liquor Gift Sets), North
Bergen, New Jersey
On January 13, 2014, the Port
Authority of New York and New Jersey,
grantee of FTZ 49, submitted a
notification of proposed production
activity to the Foreign-Trade Zones
(FTZ) Board on behalf of Western
Carriers, Inc., within FTZ 49—Site 15,
in North Bergen, New Jersey.
The notification was processed in
accordance with the regulations of the
FTZ Board (15 CFR part 400), including
notice in the Federal Register inviting
public comment (79 FR 4442,
1–28–2014). The FTZ Board has
determined that no further review of the
activity is warranted at this time. The
production activity described in the
notification is authorized, subject to the
FTZ Act and the FTZ Board’s
regulations, including Section 400.14.
Dated: May 13, 2014,
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2014–11529 Filed 5–16–14; 8:45 am]
BILLING CODE 3510–DS–P
DEPARTMENT OF COMMERCE
International Trade Administration
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[A–570–014]
53-Foot Domestic Dry Containers From
the People’s Republic of China:
Initiation of Antidumping Duty
Investigation
Enforcement and Compliance,
International Trade Administration,
Department of Commerce.
DATES: Effective Date: May 19, 2014.
AGENCY:
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17:17 May 16, 2014
Jkt 232001
John
Drury and Brian Davis, Office VI, AD/
CVD Operations, Enforcement and
Compliance, International Trade
Administration, U.S. Department of
Commerce, 14th Street and Constitution
Avenue NW., Washington, DC 20230;
telephone: (202) 482–0195 and (202)
482–7924, respectively.
SUPPLEMENTARY INFORMATION:
FOR FURTHER INFORMATION CONTACT:
The Petition
On April 23, 2014, the Department of
Commerce (Department) received an
antidumping duty (AD) petition
concerning imports of 53-foot domestic
dry containers (domestic dry containers)
from the People’s Republic of China
(PRC), officially filed in proper form on
behalf of a U.S. producer of domestic
dry containers, Stoughton Trailers, LLC
(Petitioner).1 The AD Petition was
accompanied by a countervailing duty
(CVD) petition concerning imports of
domestic dry containers from the PRC.
On April 25, 2014, and May 6, 2014, the
Department requested additional
information and clarification of certain
areas of the Petition, and on April 30,
2014, and May 8, 2014, respectively,
Petitioner filed responses to these
requests.2
In accordance with section 732(b) of
the Tariff Act of 1930, as amended (the
Act), Petitioner alleges that imports of
domestic dry containers from the PRC
are being, or are likely to be, sold in the
United States at less than fair value
within the meaning of section 731 of the
Act, and that such imports materially
retard the establishment of an industry
in the United States, or in the
alternative, that the U.S. industry is
materially injured or threatened with
material injury by reason of such
imports. Also, consistent with section
732(b)(1) of the Act, the Petition is
accompanied by information reasonably
available to Petitioner in support of its
allegations.
The Department finds that Petitioner
filed the Petition on behalf of the
domestic industry because Petitioner is
1 See ‘‘Petition for the Imposition of Antidumping
Duties on Imports of 53-Foot Domestic Dry
Containers from the People’s Republic of China,’’
dated April 23, 2014 (hereafter referred to as the
‘‘Petition’’).
2 See Petitioner’s, filing titled, ‘‘Response to
Department of Commerce Supplemental Questions,
Volume II: Sales at Less Than Normal Value,’’ dated
April 30, 2014 (AD Supplement); see also
‘‘Response to Department of Commerce
Supplemental Questions, Volume I: General
Issues,’’ dated April 30, 2014 (General Issues
Supplement); and ‘‘Petition for the Imposition of
Antidumping and Countervailing Duties,
Supplemental Submission, Petition Volume II: 53Foot Domestic Dry Containers from the People’s
Republic of China’’, dated May 8, 2014 (AD
Supplement 2).
PO 00000
Frm 00004
Fmt 4703
Sfmt 4703
an interested party as defined in section
771(9)(C) of the Act, and that Petitioner
demonstrated sufficient industry
support with respect to the initiation of
the AD investigation that Petitioner is
requesting.3
Period of Investigation
The period of investigation (POI) is
October 1, 2013, through March 31,
2014.
Scope of the Investigation
The product covered by this
investigation is domestic dry containers
from the PRC. For a full description of
the scope of the investigation, please see
the ‘‘Scope of the Investigation’’ in
Appendix I of this notice.
Comments on the Scope of the
Investigation
During our review of the Petition, the
Department issued questions to, and
received responses from, Petitioner
pertaining to the proposed scope
language in order to ensure that such
language is an accurate reflection of the
product for which the domestic industry
is seeking relief.4 As discussed in the
preamble to the Department’s
regulations,5 we are setting aside a
period for interested parties to raise
issues regarding product coverage. The
period of scope comments is intended to
provide the Department with ample
opportunity to consider all comments
and to consult with parties prior to the
issuance of the preliminary
determination. All comments must be
filed by 5:00 p.m. Eastern Daylight Time
(EDT) on June 2, 2014, which is twenty
calendar days from the signature date of
this notice. Any rebuttal comments
must be filed by 5:00 p.m. EDT on June
9, 2014. All such comments must be
filed on the records of the AD
investigation, as well as the concurrent
CVD investigation.
Filing Requirements
All comments and submissions to the
Department must be filed electronically
using Enforcement and Compliance’s
Antidumping and Countervailing Duty
Centralized Electronic Service System
(IA ACCESS). An electronically filed
document must be received successfully
in its entirety by the time and date of
the applicable deadline noted above.
Documents excepted from the electronic
submission requirements must be filed
3 See ‘‘Determination of Industry Support for the
Petition’’ section, below.
4 See General Issues Supplemental Questions,
dated April 25, 2014; see also General Issues
Supplement, at 1–2 and Exhibit SG–2.
5 See Antidumping Duties; Countervailing Duties;
Final Rule, 62 FR 27296, 27323 (May 19, 1997).
E:\FR\FM\19MYN1.SGM
19MYN1
Agencies
[Federal Register Volume 79, Number 96 (Monday, May 19, 2014)]
[Notices]
[Pages 28672-28674]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-11453]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
Bureau of Economic Analysis
Proposed Information Collection; Comment Request; Survey:
Expenditures Incurred by Recipients of Biomedical Research and
Development Awards From the National Institutes of Health (NIH)
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Department of Commerce, as part of its continuing effort
to reduce paperwork and respondent burden, invites the general
[[Page 28673]]
public and other Federal agencies to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995, Public Law 104-13 (44 U.S.C. 3506(c)(2)(A)).
DATES: Written comments must be submitted on or before July 18, 2014.
ADDRESSES: Direct all written comments to Jennifer Jessup, Departmental
Paperwork Clearance Officer, Department of Commerce, Room 6616, 14th
and Constitution Avenue NW., Washington, DC 20230, or via email at
jjessup@doc.gov.
FOR FURTHER INFORMATION CONTACT: Jennifer A. Bennett, Chief, Government
Fixed Assets Branch, Government Division (BE-57), Bureau of Economic
Analysis, U.S. Department of Commerce, Washington, DC 20230; phone:
(202) 606-9769; fax: (202) 606-5369; or via email at
jennifer.bennett@bea.gov.
SUPPLEMENTARY INFORMATION:
I. Abstract
The survey obtains the distribution of expenditures incurred by
recipients of biomedical research awards from the National Institutes
of Health (NIH) and will provide information on how the NIH award
amounts are expended across several major categories. This information,
along with wage and price data from other published sources, will be
used to generate the Biomedical Research and Development Price Index
(BRDPI). BEA develops this index for NIH under a reimbursable contract.
The BRDPI is an index of prices paid for the labor, supplies,
equipment, and other inputs required to perform the biomedical research
the NIH supports in its intramural laboratories and through its awards
to extramural organizations. The BRDPI is a vital tool for planning the
NIH research budget and analyzing future NIH programs. A survey of
award recipients is currently the only means for updating the
expenditure category weights that are used to prepare the BRDPI.
The proposed survey change revises the instructions to clarify that
respondent's should report not only expenditures from direct NIH award
amounts, but also from NIH awards received as a sub-recipient from
another institution.
This survey will be voluntary. The authority for NIH to collect
information for the BRDPI is provided in 45 CFR subpart C, Post-Award
Requirements, Sec. 74.21. This sets forth explicit standards for
grantees in establishing and maintaining financial management systems
and records, and Sec. 74.53 which provides for the retention of such
records as well as NIH access to such records.
BEA will administer the survey and analyze the survey results on
behalf of NIH, through an interagency agreement between the two
agencies. The authority for the NIH to contract with DOC to make this
collection is the Economy Act (31 U.S.C. 1535 and 1536).
The ``Special Studies'' authority, 15 U.S.C. 1525 (first
paragraph), permits DOC to provide, upon the request of any person,
firm, or public or private organization (a) Special studies on matters
within the authority of the Department of Commerce, including preparing
from its records special compilations, lists, bulletins, or reports,
and (b) furnishing transcripts or copies of its studies, compilations
and other records. NIH's support for this research is consistent with
the Agency's duties and authority under 42 U.S.C. 282.
The information provided by the respondents will be held
confidential and be used for exclusively statistical purposes. This
pledge of confidentiality is made under the Confidential Information
Protection provisions of title V, subtitle A, Public Law 107-347. Title
V is the Confidential Information Protection and Statistical Efficiency
Act of 2002 (CIPSEA). Section 512 (on Limitations on Use and Disclosure
of Data and Information) of the Act, provides that ``data or
information acquired by an agency under a pledge of confidentiality and
for exclusively statistical purposes shall be used by officers,
employees, or agents of the agency exclusively for statistical
purposes. Data or information acquired by an agency under a pledge of
confidentiality for exclusively statistical purposes shall not be
disclosed by an agency in identifiable form, for any use other than an
exclusively statistical purpose, except with the informed consent of
the respondent.''
Responses will be kept confidential and will not be disclosed in
identifiable form to anyone, other than employees or agents of BEA or
agents of NIH, without prior written permission of the person filing
the report. By law, each employee as well as each agent is subject to a
jail term of up to 5 years, a fine of up to $250,000, or both for
disclosing to the public any identifiable information that is reported
about a business or institution.
Section 515 of the Information Quality Guidelines applies to this
survey. The collection and use of this information complies with all
applicable information quality guidelines, i.e., those of the Office of
Management and Budget, Department of Commerce, and BEA.
II. Method of Collection
A survey with a cover letter that includes a brief description of,
and rationale for, the survey will be sent by email to potential
respondents by the first week of October in 2014 and by August of 2015
and 2016. A report of the respondent's expenditures of the NIH award
amounts, including NIH awards received as a sub-recipient from another
institution, following the proposed format for expenditure categories
included with the survey form, will be requested to be completed and
submitted online no later than December 8, which in most years will be
approximately 120 days after mailing. Survey respondents will be
selected on the basis of award levels, which determine the weight of
the respondent in the biomedical research and development price index.
Potential respondents will include (1) The top 100 organizations in
total awards, which account for about 73 percent of total awards; (2)
40 additional organizations that are not primarily in the ``Research
and Development (R&D) contracts'' category; and (3) 10 additional
organizations that are primarily in the ``R&D contracts'' category.
III. Data
OMB Control Number: 0608-0069.
Form Number: None.
Type of Review: Regular submission.
Affected Public: Universities or other organizations that are NIH
award recipients.
Estimated Number of Respondents: 120.
Estimated Time per Response: 16 hours, but may vary among
respondents because of differences in institution structure, size, and
complexity.
Estimated Total Annual Burden Hours: 1,920 hours.
Estimated Total Annual Cost to Public: $0.
IV. Request for Comments
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the NIH, including whether the information has practical utility; (b)
the accuracy of the agency's estimate of the burden (including hours
and cost) of the proposed collection of information; (c) ways to
enhance the quality, utility, and clarity of the information to be
collected; and (d) ways to minimize the burden of the collection of
information on respondents, including through the use
[[Page 28674]]
of automated collection techniques or other forms of information
technology.
Comments submitted in response to this notice will be summarized
and/or included in the request for OMB approval of this information
collection; they also will become a matter of public record.
Dated: May 13, 2014.
Glenna Mickelson,
Management Analyst, Office of Chief Information Officer.
[FR Doc. 2014-11453 Filed 5-16-14; 8:45 am]
BILLING CODE 3510-EA-P