Agency Forms Undergoing Paperwork Reduction Act Review, 53877-53879 [2018-23293]
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Federal Register / Vol. 83, No. 207 / Thursday, October 25, 2018 / Notices
classification that is not listed in the
wage determination applicable to the
contract. The contractor submits to the
contracting officer a Standard Form (SF)
1444, Request for Authorization of
Additional Classification and Rate,
along with other pertinent data,
containing the proposed additional
classification and minimum wage rate
including any fringe benefits payments.
OMB control numbers 1235–0023,
1235–0008, and 1235–0018 account for
records to be kept by employers under
the Fair Labor Standards Act (FLSA), 29
CFR 516, which is the basic
recordkeeping regulation for all the laws
administered by the Department of
Labor (DOL) Wage and Hour Division.
29 CFR 516, prescribes labor standards
for federally financed and assisted
construction contracts subject to the
Davis-Bacon and Related Acts (DBRA),
as well as labor standards for nonconstruction contracts subject to the
Contract Work Hours and Safety
Standards Act (CWHSSA).
3. 52.222–11, Subcontracts (Labor
Standards), requires contractors to
submit SF 1413, Statement and
Acknowledgment, for each subcontract
for construction within the United
States, including the subcontractor’s
signed and dated acknowledgment that
the required labor clauses have been
included in the subcontract. DOL
regulations at 29 CFR Subpart 5.6
require Federal agencies to ascertain
compliance with statutes such as the
Wage Rate Requirements (Construction)
(formerly known as the Davis-Bacon
Act) (40 U.S.C. chapter 31), the
Copeland Act (Anti-Kickback) (18
U.S.C. 874 and 40 U.S.C. 3145), and the
Contract Work Hours and Safety
Standards Act (40 U.S.C. 3701 et seq.)
4. 52.222–18, Certification Regarding
Knowledge of Child Labor for Listed
End Products, requires offerors to certify
they will not supply an end product of
a type identified on the DOL List of
Products Requiring Contractor
Certification as to Forced or Indentured
Child Labor, or that the offeror will
supply such product, but made a good
faith effort to determine whether forced
or indentured child labor was used to
mine, produce, or manufacture any
product furnished under the contract
and is unaware of any such use of child
labor. For solicitations for commercial
items, the Certification Regarding
Knowledge of Child Labor for Listed
End Products is at paragraph (i) of the
provision at 52.212–3, Offeror
Representations and Certifications—
Commercial Items. This requirement is
necessary to comply with Executive
Order 13126, Prohibition of Acquisition
of Products Produced by Forced or
VerDate Sep<11>2014
19:45 Oct 24, 2018
Jkt 247001
Indentured Child Labor, signed by
President Clinton on June 12, 1999.
5. 52.222–33, Notice of Requirement
for Project Labor Agreement, and
52.222–34, Project Labor Agreement,
require offerors (provision) to submit,
and contractors (clause) to maintain, a
copy of the project labor agreement
(PLA). Agencies have discretion on
whether or not to use a PLA in
connection with large-scale construction
contracts, valued at or above $25M.
Agencies may require the PLA be
submitted: (1) When offers are due, (2)
prior to award (by the apparent
successful offeror), or (3) after award.
6. 52.222–46, Evaluation of
Compensation for Professional
Employees. This provision requires
offerors to submit for evaluation a total
compensation plan setting forth
proposed salaries and fringe benefits for
professional employees working on the
contract. This is required for negotiated
service contracts when the contract
amount is expected to exceed $700,000
and the service to be provided will
require meaningful numbers of
professional employees.
C. Annual Reporting Burden
1. 52.222–2, Payment for Overtime
Premiums.
Respondents: 2,098.
Responses per Respondent: 1.
Total annual Responses: 2,098.
Hours per Response: 0.25.
Total Burden Hours: 525.
2. FAR 52.222–6 and SF 1,444 Request
for Authorization of Additional
Classification and Rate.
Respondents: 3,831.
Responses per Respondent: 2.
Total Annual Responses: 7,662.
Hours per Response: 0.5.
Total Burden Hours: 3,831.
3. FAR 52.222–11, Subcontracts
(Labor Standards), and SF 1413,
Statement and Acknowledgment.
Respondents: 36,553.
Responses per Respondent: 2.
Total Annual Responses: 73,106.
Hours per Response: 0.05.
Total Burden Hours: 3,655.
4. FAR 52.222–18 Certification
Regarding Knowledge of Child Labor for
Listed End Products
Respondents: 1,104.
Responses per Respondent: 1.
Total Annual Responses: 1,104.
Hours per Response: 0.18.
Total Burden Hours: 198.
5. FAR 52.222–33 and 52.222–34,
Project Labor Agreement
PO 00000
Respondents: 45.
Responses per Respondent: 1.
Frm 00031
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Sfmt 4703
53877
Total Annual Responses: 45.
Hours per Response: 1.
Total Burden Hours: 45.
6. FAR 52.222–46 Evaluation of
Compensation for Professional
Employees
Respondents: 3,136.
Responses per Respondent: 3.
Total Annual Responses: 9,408.
Hours per Response: 1.3333.
Total Burden Hours: 12,544.
7. Summary
Respondents: 46,767.
Total annual Responses: 93,423.
Total Burden Hours: 20,798.
Affected Public: Businesses or other
for-profit and not-for-profit institutions.
Obtaining Copies: 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. 9000–0066, Laborrelated Requirements, in all
correspondence.
Janet Fry,
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy,
Office of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2018–23351 Filed 10–24–18; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30 Day–19–1046]
Agency Forms Undergoing Paperwork
Reduction Act Review
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 Breast
and Cervical Cancer Early Detection
Program (NBCCEDP) Monitoring
Activities 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
26, 2018 to obtain comments from the
public and affected agencies. CDC did
not receive 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.
E:\FR\FM\25OCN1.SGM
25OCN1
53878
Federal Register / Vol. 83, No. 207 / Thursday, October 25, 2018 / Notices
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,
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 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, 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 Breast and Cervical Cancer
Early Detection Program (NBCCEDP)
Monitoring Activities (OMB No. 0920–
1046, Exp. 01/31/2018)—Reinstatement
with Change—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC requests a Reinstatement with
Change, of an information collection
previously approved under OMB
Control Number 0920–1046.
Information collection within the
previous OMB approval period
consisted of an annual grantee survey.
Information collection within the next
OMB approval period will consist of a
redesigned survey and a new cliniclevel data collection. The number of
respondents will increase from 67 to 70,
and the total estimated annualized
burden will increase from 45 hours to
683 hours.
In 2014, more than 236,000 women
were diagnosed with breast cancer, and
more than 12,000 women were
diagnosed with cervical cancer.
Evidence shows that deaths from both
breast and cervical cancers can be
avoided by increasing screening services
among women. However, screening is
typically underutilized among women
who are under- or uninsured, have no
regular source of healthcare, or who
recently immigrated to the U.S.
To improve access to cancer
screening, Congress passed the Breast
and Cervical Cancer Mortality
Prevention Act of 1990 (Pub. L. 101–
354), which directed CDC to create the
National Breast and Cervical Cancer
Early Detection Program (NBCCEDP).
The NBCCEDP currently provides
funding to 70 grantees under ‘‘Cancer
Prevention and Control Programs for
State, Territorial, and Tribal
Organizations (DP17–1701).’’ The
purpose of NBCCEDP is to increase
breast and cervical cancer screening
rates among women residing within
defined geographical locations (as
determined by the funded program) who
are at or below 250% of the federal
poverty level; aged 40–64 years for
breast cancer services, and aged 21–64
years for cervical cancer services; and
under- or uninsured.
The NBCCEDP was significantly
redesigned in 2017 to expand its focus
on direct service provision to include
implementation of evidence-based
interventions (EBIs) intended to
increase breast and cervical cancer
screening at the population level. Based
on the redesigned NBCCEDP, the
information collection plan has also
been redesigned.
The proposed information collection
includes: (1) An annual NBCCEDP
Grantee Survey revised to reflect the
focus of the redesigned program under
DP17–1701, and (2) CDC clinic-level
data will assess EBI implementation and
the NBCCEDP’s primary outcome of
interest—breast and cervical screening
rates within partner health system
clinics—at baseline and annually.
NBCCEDP grantees will collect and
report data for all partnering health
system clinic sites—an estimated 6
clinics per grantee for breast cancer data
and 6 clinics per grantee for cervical
cancer data.
The proposed information collections
will allow CDC to gauge progress in
meeting NBCCEDP program goals and
monitor implementation activities,
evaluate outcomes, and identify grantee
technical assistance needs. In addition,
findings will inform program
improvement and help identify
successful activities that need to be
maintained, replicated, or expanded.
OMB approval is requested for three
years. Participation is required for
NBCCEDP grantees. There are no costs
to respondents other than their time.
The total estimated annualized burden
hours are 683.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondent
Form name
NBCCEDP Grantees ..............
NBCCEDP Grantees ..............
NBCCEDP Grantee Survey ...................................................
NBCCEDP Clinic-level Information Collection Instrument—
Breast.
NBCCEDP Clinic-level Information Collection Instrument—
Cervical.
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NBCCEDP Grantees ..............
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Number of
respondents
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E:\FR\FM\25OCN1.SGM
Number of
responses per
respondent
Average
burden per
response
(in hr)
70
70
1
6
45/60
45/60
70
6
45/60
25OCN1
53879
Federal Register / Vol. 83, No. 207 / Thursday, October 25, 2018 / Notices
Jeffrey M. Zirger,
Acting 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. 2018–23293 Filed 10–24–18; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–19–0920]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Data Collection
Through Web Based Surveys for
Evaluating Act Against AIDS Social
Marketing Campaign Phases Targeting
Consumers 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 June 6,
2018 to obtain comments from the
public and affected agencies. CDC
received one comment 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, 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 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, 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
Data Collection Through Web Based
Surveys for Evaluating Act Against
AIDS Social Marketing Campaign
Phases Targeting Consumers (OMB
#0920–0920, Exp. 6/30/2018)—
Reinstatement with Change—National
Center for HIV/AIDS, Viral Hepatitis,
STD and TB Prevention (NCHHSTP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In response to the continued HIV
epidemic in our country, CDC launched
Act Against AIDS (AAA), a multifaceted
communication campaign to reduce HIV
incidence in the United States in 2009.
CDC has released the campaign in
phases, with some of the phases running
concurrently. Each phase of the
campaign uses mass media and directto-consumer channels to deliver
messages. Some campaigns provide
basic education and increase awareness
of HIV/AIDS among the general public,
whereas others emphasize HIV
prevention and testing among specific
subgroups or communities at greatest
risk of infection. CDC will also develop
new messages to address changes in
prevention science and subpopulations
affected by HIV. The proposed study
will assess the effectiveness of these
social marketing messages aimed at
increasing HIV/AIDS awareness,
increasing prevention behaviors, and
improving HIV testing rates among
consumers.
The reinstatement with change of this
ongoing study will allow for continued
evaluation of the effectiveness of AAA
social marketing campaign through
surveys with consumers. A total of
10,750 respondents were approved for
the previously renewed generic ICR
(0920–0920) and since the approval
date, 4,305 respondents were surveyed
under the GenIC, ‘‘Development of
Messages for the Act Against AIDS
National Testing’’. The information
collected from these data collections
was used to evaluate a specific AAA
campaign phase. We are requesting the
same amount of time to continue
surveying AAA target audiences as new
phases are developed.
Through the continuation of this
collection, we plan to reach the
remaining approved 6,445 respondents.
To obtain the remaining respondents,
we anticipate screening approximately
32,220 individuals. Depending on the
target audience for the campaign phase,
the study screener will vary. The study
screener may address one or more of the
following items: Race/ethnicity, sexual
behavior, sexual orientation, gender
identity, HIV testing history, HIV status,
and injection drug use. Each survey will
have a core set of items asked in all
rounds, as well as a module of questions
relating to specific AAA phases and
activities.
Respondents will be recruited through
national opt-in email lists, the internet,
and external partnerships with
community-based and membership
organizations that work with or
represent individuals from targeted
populations (e.g., National Urban
League, the National Medical
Association). Respondents will selfadminister the survey at home on
personal computers. There is no cost to
the respondents other than their time.
The total annualized burden hours are
1,432.
daltland on DSKBBV9HB2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Individuals (male and female) aged 18 years and older ...........................
Study Screener ...
Survey .................
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Sfmt 4703
Number of
respondents
10,740
2,148
E:\FR\FM\25OCN1.SGM
25OCN1
Number of
responses per
respondent
1
1
Average
burden per
response
(in hours)
2/60
30/60
]]>Agencies
[Federal Register Volume 83, Number 207 (Thursday, October 25, 2018)]
[Notices]
[Pages 53877-53879]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-23293]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30 Day-19-1046]
Agency Forms Undergoing Paperwork Reduction Act Review
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 Breast and Cervical Cancer Early
Detection Program (NBCCEDP) Monitoring Activities 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 26, 2018 to obtain comments from
the public and affected agencies. CDC did not receive 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.
[[Page 53878]]
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, 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 or send an email to [email protected]. 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 Breast and Cervical Cancer Early Detection Program
(NBCCEDP) Monitoring Activities (OMB No. 0920-1046, Exp. 01/31/2018)--
Reinstatement with Change--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
CDC requests a Reinstatement with Change, of an information
collection previously approved under OMB Control Number 0920-1046.
Information collection within the previous OMB approval period
consisted of an annual grantee survey. Information collection within
the next OMB approval period will consist of a redesigned survey and a
new clinic-level data collection. The number of respondents will
increase from 67 to 70, and the total estimated annualized burden will
increase from 45 hours to 683 hours.
In 2014, more than 236,000 women were diagnosed with breast cancer,
and more than 12,000 women were diagnosed with cervical cancer.
Evidence shows that deaths from both breast and cervical cancers can be
avoided by increasing screening services among women. However,
screening is typically underutilized among women who are under- or
uninsured, have no regular source of healthcare, or who recently
immigrated to the U.S.
To improve access to cancer screening, Congress passed the Breast
and Cervical Cancer Mortality Prevention Act of 1990 (Pub. L. 101-354),
which directed CDC to create the National Breast and Cervical Cancer
Early Detection Program (NBCCEDP). The NBCCEDP currently provides
funding to 70 grantees under ``Cancer Prevention and Control Programs
for State, Territorial, and Tribal Organizations (DP17-1701).'' The
purpose of NBCCEDP is to increase breast and cervical cancer screening
rates among women residing within defined geographical locations (as
determined by the funded program) who are at or below 250% of the
federal poverty level; aged 40-64 years for breast cancer services, and
aged 21-64 years for cervical cancer services; and under- or uninsured.
The NBCCEDP was significantly redesigned in 2017 to expand its
focus on direct service provision to include implementation of
evidence-based interventions (EBIs) intended to increase breast and
cervical cancer screening at the population level. Based on the
redesigned NBCCEDP, the information collection plan has also been
redesigned.
The proposed information collection includes: (1) An annual NBCCEDP
Grantee Survey revised to reflect the focus of the redesigned program
under DP17-1701, and (2) CDC clinic-level data will assess EBI
implementation and the NBCCEDP's primary outcome of interest--breast
and cervical screening rates within partner health system clinics--at
baseline and annually. NBCCEDP grantees will collect and report data
for all partnering health system clinic sites--an estimated 6 clinics
per grantee for breast cancer data and 6 clinics per grantee for
cervical cancer data.
The proposed information collections will allow CDC to gauge
progress in meeting NBCCEDP program goals and monitor implementation
activities, evaluate outcomes, and identify grantee technical
assistance needs. In addition, findings will inform program improvement
and help identify successful activities that need to be maintained,
replicated, or expanded.
OMB approval is requested for three years. Participation is
required for NBCCEDP grantees. There are no costs to respondents other
than their time. The total estimated annualized burden hours are 683.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hr)
----------------------------------------------------------------------------------------------------------------
NBCCEDP Grantees................... NBCCEDP Grantee Survey..... 70 1 45/60
NBCCEDP Grantees................... NBCCEDP Clinic-level 70 6 45/60
Information Collection
Instrument--Breast.
NBCCEDP Grantees................... NBCCEDP Clinic-level 70 6 45/60
Information Collection
Instrument--Cervical.
----------------------------------------------------------------------------------------------------------------
[[Page 53879]]
Jeffrey M. Zirger,
Acting 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. 2018-23293 Filed 10-24-18; 8:45 am]
BILLING CODE 4163-18-P
