60-day Federal Register Notice

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Federal Register / Vol. 87, No. 93 / Friday, May 13, 2022 / Notices

and National Aeronautics and Space
Administration (NASA).

A. OMB Control Number, Title, and
Any Associated Form(s)

Notice and request for
comments.

9000–0029, Extraordinary Contractual
Action Requests.

In accordance with the
Paperwork Reduction Act of 1995, and
the Office of Management and Budget
(OMB) regulations, DoD, GSA, and
NASA invite the public to comment on
an extension concerning extraordinary
contractual action requests. DoD, GSA,
and NASA invite comments on:
Whether the proposed collection of
information is necessary for the proper
performance of the functions of Federal
Government acquisitions, including
whether the information will have
practical utility; the accuracy of the
estimate of the burden of the proposed
information collection; ways to enhance
the quality, utility, and clarity of the
information to be collected; and ways to
minimize the burden of the information
collection on respondents, including the
use of automated collection techniques
or other forms of information
technology. OMB has approved this
information collection for use through
September 30, 2022. DoD, GSA, and
NASA propose that OMB extend its
approval for use for three additional
years beyond the current expiration
date.

B. Need and Uses

ACTION:

SUMMARY:

DoD, GSA, and NASA will
consider all comments received by July
12, 2022.

DATES:

DoD, GSA, and NASA
invite interested persons to submit
comments on this collection through
https://www.regulations.gov and follow
the instructions on the site. This website
provides the ability to type short
comments directly into the comment
field or attach a file for lengthier
comments. If there are difficulties
submitting comments, contact the GSA
Regulatory Secretariat Division at 202–
501–4755 or GSARegSec@gsa.gov.
Instructions: All items submitted
must cite OMB Control No. 9000–0029,
Extraordinary Contractual Action
Requests. 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.

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ADDRESSES:

FOR FURTHER INFORMATION CONTACT:

Marissa Ryba, Procurement Analyst, at
telephone 314–586–1280, or
marissa.ryba@gsa.gov.
SUPPLEMENTARY INFORMATION:

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This justification supports an
extension of OMB Control No. 9000–
0029. This clearance covers the
information that contractors must
submit to comply with the following
Federal Acquisition Regulation (FAR)
requirements:
FAR 50.103–3, Contract Adjustment.
FAR 50.103–3 specifies the minimum
information that a contractor must
include when seeking a contract
adjustment that would facilitate the
national defense, as set forth in Public
Law 85–804. The request, normally a
letter, shall state as a minimum—
(1) The precise adjustment requested;
(2) The essential facts, summarized
chronologically in narrative form;
(3) The contractor’s conclusions based
on these facts, showing, in terms of the
considerations set forth in FAR 50.103–
1 and 50.103–2, when the contractor
considers itself entitled to the
adjustment; and
(4) Whether or not—
(i) All obligations under the contracts
involved have been discharged;
(ii) Final payment under the contracts
involved has been made;
(iii) Any proceeds from the request
will be subject to assignment or other
transfer, and to whom; and
(iv) The contractor has sought the
same, or a similar or related, adjustment
from the Government Accountability
Office or any other part of the
Government, or anticipates doing so.
If the request exceeds the simplified
acquisition threshold, the contractor
must certify that the request is made in
good faith and the data are accurate and
complete.
FAR 50.103–4, Facts and Evidence.
FAR 50.103–4 sets forth additional
information that the contracting officer
or other agency official may request
from the contractor to support any
request made under FAR 50.103–3.
FAR 50.104–3 Special Procedures for
Unusually Hazardous or Nuclear Risks.
FAR 50.104–3 provides the information
a contractor shall submit to the
contracting officer when requesting the
inclusion of the indemnification clause
for unusually hazardous or nuclear risks
at FAR 52.250–1.
FAR 52.250–1, Indemnification Under
Public Law 85–804. This clause allows
contractors to be indemnified against
unusually hazardous or nuclear risks.
Paragraph (g) requires the contractor to
promptly notify the contracting officer

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and furnish pertinent information for
any claim or loss that may involve
indemnification under the clause.
This information is used by the
Government to determine if relief can be
granted to the contractor and to
determine the appropriate type and
amount of relief.
C. Annual Burden
Respondents: 28.
Total Annual Responses: 165.
Total Burden Hours: 6,848.
Obtaining Copies: Requesters may
obtain a copy of the information
collection documents from the GSA
Regulatory Secretariat Division by
calling 202–501–4755 or emailing
GSARegSec@gsa.gov. Please cite OMB
Control No. 9000–0029, Extraordinary
Contractual Action Requests.
Janet Fry,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2022–10368 Filed 5–12–22; 8:45 am]
BILLING CODE 6820–EP–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–22FI; Docket No. CDC–2022–
0064]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:

The Centers for Disease
Control and Prevention (CDC), located
within the Department of Health and
Human Services (HHS), as part of its
continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other federal
agencies the opportunity to comment on
a proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled National HIV
Behavioral Surveillance: Brief HIV Biobehavioral Assessment (NHBS–BHBA).
CDC is requesting approval to collect
data on behaviors related to HIV
infection and prevention among priority
populations at high risk for HIV using
mixed methods in selected geographic

SUMMARY:

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Federal Register / Vol. 87, No. 93 / Friday, May 13, 2022 / Notices
areas across two funded states in the
United States.
DATES: CDC must receive written
comments on or before July 12, 2022.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0064, by either of the following
methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:

1. 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;
2. Evaluate the accuracy of the agency’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and assumptions
used;
3. Enhance the quality, utility, and clarity
of the information to be collected;
4. 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 submissions of
responses; and
5. Assess information collection costs.

Project teams will conduct brief
standardized quantitative interviews
and anonymous HIV blood-based rapid
testing and supplemental testing to
those who participate in quantitative
data collection to assess HIV
seroprevalence. The data from the
quantitative interviews will provide
estimates of: (1) Behavior related to the
risk of HIV and other sexually
transmitted diseases, (2) prior testing for
HIV, and (3) use of HIV prevention
services. HIV screening results will be
made available to participants, and
those with preliminary positive test
results will be linked to HIV care.
Qualitative data collection includes key
informant interviews with community
members and professionals familiar
with the population and focus groups to
interpret standardized quantitative
findings and inform grantee-developed
recommendations for state/local public
health partners. The data from
qualitative interviews will be used to
interpret standardized quantitative
findings and inform recipient-developed
recommendations for state and local
public health authorities. No other
federal agency collects this type of
information in the populations at high
risk in these selected geographic areas
using mixed methods of quantitative
and qualitative interviews.
CDC estimates that during
quantitative interviewing, 1338
individuals will complete the
quantitative base eligibility screener,
1204 will complete the quantitative
population eligibility screener, and 338
will be either not interested or
ineligible, yielding a total of 1,000
eligible respondents over a 12-month
period. Because HIV testing is a clinical
procedure, it is not included in the
burden estimates. For qualitative data
collection, approximately 96
individuals will complete the eligibility
screener, 16 of the respondents will be
either not interested in completing a
qualitative interview, or will be
ineligible, yielding a total of 80 eligible
respondents over a 12-month period.
CDC requests OMB approval for an
estimated 497 annual burden hours.
Participation of respondents is
voluntary, and there are no costs to
respondents other than their time.

Proposed Project
National HIV Behavioral Surveillance:
Brief HIV Bio-behavioral Assessment
(NHBS–BHBA)—New—National Center
for HIV, Viral Hepatitis, STD, and TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The purpose of this data collection is
to monitor behaviors of populations at
high risk for Human Immunodeficiency
Virus (HIV) infection using mixedmethods in selected geographic areas in
the United States which lack
biobehavioral data related to HIV
transmission and prevention.
Preventing HIV, especially among
populations at high risk, is an effective
strategy for reducing individual, local,
and national healthcare costs. The
utility of this information is to provide
CDC and health department staff with
data for evaluating progress towards
state public health goals, such as
reducing new HIV infections, increasing
the use of condoms, and focusing on
populations at high risk by describing
and monitoring the HIV risk behaviors,
HIV seroprevalence and incidence, and
HIV prevention experiences of persons
at highest risk for HIV infection. Data
will be systematically collected using
mixed methods of quantitative and
qualitative interviews. Brief screening
interviews will be used to determine
eligibility for participation in the
quantitative and qualitative interviews.

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ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondents

Form name

Persons Screened .................
Persons Screened .................
Eligible Participants ...............

Quantitative Base Eligibility Screener ..........
Quantitative Population Eligibility Screener
Quantitative Core Survey .............................

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Number of
responses per
respondent

1,338
1,204
1,000

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1
1
1

13MYN1

Average
burden per
response
(in hours)
1/60
5/60
10/60

Total burden
(in hours)
23
101
167

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Federal Register / Vol. 87, No. 93 / Friday, May 13, 2022 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Total burden
(in hours)

Form name

Eligible Participants ...............
Persons Screened .................
Eligible Participant .................

Quantitative Population-specific Questions
Qualitative Eligibility Screener .....................
Qualitative Interviews ...................................

1,000
96
80

1
1
1

5/60
1/60
90/60

84
2
120

Total ...............................

.......................................................................

........................

........................

........................

497

Jeffery M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–10380 Filed 5–12–22; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–22–0213]

Agency Forms Undergoing Paperwork
Reduction Act Review

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Average
burden per
response
(in hours)

Number of
responses per
respondent

Number of
respondents

Type of respondents

In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘National Vital
Statistics Report Form’’ to the Office of
Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on January 7,
2022 to obtain comments from the
public and affected agencies. CDC did
not receive any comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(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
agencies estimate of the burden of the
proposed collection of information,

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including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the 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.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
National Vital Statistics Report Form
(OMB Control No. 0920–0213, Exp. 10/
31/2023)—Revision—National Center
for Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The compilation of national vital
statistics dates back to the beginning of
the 20th Century and has been

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conducted since 1960 by the Division of
Vital Statistics of the National Center for
Health Statistics (NCHS), CDC. The
collection of this data is authorized by
42 U.S.C. 242k, and this submission
requests to continue use of the Annual
Vital Statistics Report Form for
collection of annual marriage and
divorce/annulment summary statistics
for three years. Additionally, this
Revision requests to discontinue the
Monthly Vital Statistics Report, which
is currently used to provide counts of
monthly occurrences of births, deaths,
and infant deaths. The collection of the
provisional birth and death data is now
being achieved on a more timely,
ongoing basis which negates the need to
continue to use the monthly form.
Continued use of the Annual Vital
Statistics Report Form collects final
annual counts of marriages and divorces
by month for the United States and for
each State. These final counts are
usually available from State or county
officials about eight months after the
end of the data year. The data are
widely used by the Department of
Health and Human Services (HHS), and
other government, academic, private
research, and commercial organizations
in tracking changes in trends of family
formation and dissolution. Respondents
for the Annual Vital Statistics Reports
Form are registration officials in all 50
States, seven U.S. Territories, including
American Samoa, Guam, Northern
Mariana Islands, Puerto Rico, Virgin
Islands, the District of Columbia, and
New York City, as well as the 33 local
(county clerk) officials in New Mexico
who record marriages occurring and
divorces and annulments granted in
each county of New Mexico.
CDC requests OMB approval for an
estimated 46 annual burden hours.
There are no costs to respondents other
than their time to participate.

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