Agency Forms Undergoing Paperwork Reduction Act Review, 32329-32330 [2016-12053]
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Federal Register / Vol. 81, No. 99 / Monday, May 23, 2016 / Notices
Additionally submit a copy to GSA 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 9000–0077, Quality
Assurance Requirements’’. Follow the
instructions provided at the ‘‘Submit a
Comment’’ screen. Please include your
name, company name (if any), and
‘‘Information Collection 9000–0077,
Quality Assurance Requirements’’ on
your attached document.
• Mail: General Services
Administration, Regulatory Secretariat
Division (MVCB), 1800 F Street NW.,
Washington, DC 20405. ATTN: Ms.
Flowers/IC 9000–0077, Quality
Assurance Requirements.
Instructions: Please submit comments
only and cite Information Collection
9000–0077, Quality Assurance
Requirements, 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 email curtis.glover@
gsa.gov.
Responses per Respondent: 1.03226.
Total Responses: 142,753.
Hours per Response: .83511.
Total Burden hours: 119,214.
Affected Public: Businesses or other
for-profit and not-for-profit institutions.
Frequency: On occasion.
SUPPLEMENTARY INFORMATION:
BILLING CODE 6820–EP–P
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. 9000–0077,
Quality Assurance Requirements, in all
correspondence.
Dated: May 17, 2016.
Lorin S. Curit,
Director, Federal Acquisition Policy, Office
of Governmentwide Acquisition Policy, Office
of Acquisition Policy, Office of
Governmentwide Policy.
[FR Doc. 2016–12002 Filed 5–20–16; 8:45 am]
sradovich on DSK3TPTVN1PROD with NOTICES
A. Purpose
Supplies and services acquired under
Government contracts must conform to
the contract’s quality and quantity
requirements. FAR Part 46 prescribes
inspection, acceptance, warranty, and
other measures associated with quality
requirements. Standard clauses related
to inspection require the contractor to
provide and maintain an inspection
system that is acceptable to the
Government; gives the Government the
right to make inspections and test while
work is in process; and requires the
contractor to keep complete, and make
available to the Government, records of
its inspection work. A notice was
published in the Federal Register at 81
FR 11794 on March 7, 2016. No
comments were received.
B. Annual Reporting Burden
Respondents: 138,292.
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18:25 May 20, 2016
Jkt 238001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–16–16BX]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
PO 00000
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32329
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (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. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Monitoring and Reporting System
(MRS) for Rape Prevention and
Education (RPE) Program Awardees—
New—National Center for Injury
Prevention and Control NCIPC), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
Sexual violence (SV) is a major public
health problem, but it is preventable.
According to CDC’s National Intimate
Partner and Sexual Violence Survey
(NISVS), nearly 1 in 5 women and 1 in
71 men in the U.S. have been raped
during their lifetime, and nearly 1 in 2
women and 1 in 5 men have
experienced severe SV victimization
other than rape at some point in their
lives. The majority of victimization
starts early in life with approximately
80% of female victims experiencing
their first rape before the age of 25, and
almost half experiencing their first rape
before the age of 18.
CDC’s RPE Program is a national
initiative that addresses SV through
cooperative agreement funding and
technical assistance to health
E:\FR\FM\23MYN1.SGM
23MYN1
32330
Federal Register / Vol. 81, No. 99 / Monday, May 23, 2016 / Notices
departments in all 50 states, the District
of Columbia, and four territories (e.g.,
Guam, Puerto Rico, U.S. Virgin Islands,
and the Commonwealth of Northern
Mariana Islands) to conduct state-,
district-, and territorial-wide SV
prevention activities. The Violence
against Women Act of 1994 (VAWA)
and as amended in the Violence Against
Women Reauthorization Act of 2013
authorize the RPE program and
legislatively states that awardees will
allot RPE funds for prevention activities
conducted by local organizations (i.e.,
RPE sub-awardees), which include rape
crisis centers; State, territorial, or tribal
sexual assault coalitions; and other
public and private nonprofit entities
(e.g., community-based organizations,
nongovernmental organizations, and
academic institutions).
The CDC seeks a three-year OMB
approval to collect information from 55
RPE awardees (health departments in all
50 states, District of Columbia, and four
U.S. territories, i.e., Guam, Puerto Rico,
U.S. Virgin Islands, and the
Commonwealth of Northern Mariana
Islands) and their designees. RPE
awardees will report activity
information to CDC annually through
the Monitoring and Reporting System
(MRS), which consists of two reporting
tools, Work Plan Tool and Program
Report Tool. The Work Plan Tool
consists of items about awardees’
annual goals, objectives, progress, and
performance towards overall
cooperative agreement purpose and
strategies. The Program Report Tool
consists of items to assess awardees’
implementation, use of evidence-based
prevention strategies, and use of the
public health approach. The tools in the
MRS provide a systematic format to
collect data related to implementation
and performance consistently across all
awardees.
Information to be collected will
provide crucial data for program
performance monitoring, will allow
CDC analyze and synthesize information
across multiple RPE programs, help
ensure consistency in documenting
progress and TA, enhance
accountability of the use of federal
funds, and provide timely reports as
frequently requested by HHS, the White
House, and Congress. It provides CDC
with the capacity to respond in a timely
manner to requests for information
about the program, improve real-time
communications between CDC and RPE
awardees, and strengthen CDC’s ability
to monitor and evaluate awardees’
progress and performance.
The estimated annual burden hours
are 654. There is no cost to respondents
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses
per respondent
Average
burden
per response
(in hours)
Type of respondents
Form name
RPE Program Awardees .........................................................
(State, District of Columbia, and Territorial Health Departments) and Designees.
Work Plan Tool—Initial ..........
18
1
10
Program Report Tool—Initial
Work Plan Tool—Annual Reporting.
Program Report Tool—Annual
Reporting.
18
55
1
1
8
3
55
1
3
Leroy A. Richardson,
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. 2016–12053 Filed 5–20–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16AJE; Docket No. CDC–2016–
0043]
sradovich on DSK3TPTVN1PROD with NOTICES
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), as part of
its continuing efforts to reduce public
SUMMARY:
VerDate Sep<11>2014
18:25 May 20, 2016
Jkt 238001
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the proposed National
Health and Nutrition Examination
Survey (NHANES) Longitudinal
Study—Feasibility Component. This
project will provide a logistical test of
proposed survey procedures along with
contact, interview, and examination
rates for a sample of previously
examined NHANES participants. The
information obtained will be used to
determine the feasibility of conducting
future follow-up surveys.
DATES: Written comments must be
received on or before July 22, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0043 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Leroy A. Richardson, the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 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
E:\FR\FM\23MYN1.SGM
23MYN1
]]>Agencies
[Federal Register Volume 81, Number 99 (Monday, May 23, 2016)]
[Notices]
[Pages 32329-32330]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-12053]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-16-16BX]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for the proposed
information collection is published to obtain comments from the public
and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (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. Written comments and/or
suggestions regarding the items contained in this notice should be
directed to the Attention: CDC Desk Officer, Office of Management and
Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written
comments should be received within 30 days of this notice.
Proposed Project
Monitoring and Reporting System (MRS) for Rape Prevention and
Education (RPE) Program Awardees--New--National Center for Injury
Prevention and Control NCIPC), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Sexual violence (SV) is a major public health problem, but it is
preventable. According to CDC's National Intimate Partner and Sexual
Violence Survey (NISVS), nearly 1 in 5 women and 1 in 71 men in the
U.S. have been raped during their lifetime, and nearly 1 in 2 women and
1 in 5 men have experienced severe SV victimization other than rape at
some point in their lives. The majority of victimization starts early
in life with approximately 80% of female victims experiencing their
first rape before the age of 25, and almost half experiencing their
first rape before the age of 18.
CDC's RPE Program is a national initiative that addresses SV
through cooperative agreement funding and technical assistance to
health
[[Page 32330]]
departments in all 50 states, the District of Columbia, and four
territories (e.g., Guam, Puerto Rico, U.S. Virgin Islands, and the
Commonwealth of Northern Mariana Islands) to conduct state-, district-,
and territorial-wide SV prevention activities. The Violence against
Women Act of 1994 (VAWA) and as amended in the Violence Against Women
Reauthorization Act of 2013 authorize the RPE program and legislatively
states that awardees will allot RPE funds for prevention activities
conducted by local organizations (i.e., RPE sub-awardees), which
include rape crisis centers; State, territorial, or tribal sexual
assault coalitions; and other public and private nonprofit entities
(e.g., community-based organizations, nongovernmental organizations,
and academic institutions).
The CDC seeks a three-year OMB approval to collect information from
55 RPE awardees (health departments in all 50 states, District of
Columbia, and four U.S. territories, i.e., Guam, Puerto Rico, U.S.
Virgin Islands, and the Commonwealth of Northern Mariana Islands) and
their designees. RPE awardees will report activity information to CDC
annually through the Monitoring and Reporting System (MRS), which
consists of two reporting tools, Work Plan Tool and Program Report
Tool. The Work Plan Tool consists of items about awardees' annual
goals, objectives, progress, and performance towards overall
cooperative agreement purpose and strategies. The Program Report Tool
consists of items to assess awardees' implementation, use of evidence-
based prevention strategies, and use of the public health approach. The
tools in the MRS provide a systematic format to collect data related to
implementation and performance consistently across all awardees.
Information to be collected will provide crucial data for program
performance monitoring, will allow CDC analyze and synthesize
information across multiple RPE programs, help ensure consistency in
documenting progress and TA, enhance accountability of the use of
federal funds, and provide timely reports as frequently requested by
HHS, the White House, and Congress. It provides CDC with the capacity
to respond in a timely manner to requests for information about the
program, improve real-time communications between CDC and RPE awardees,
and strengthen CDC's ability to monitor and evaluate awardees' progress
and performance.
The estimated annual burden hours are 654. There is no cost to
respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
RPE Program Awardees.................. Work Plan Tool--Initial. 18 1 10
(State, District of Columbia, and
Territorial Health Departments) and
Designees.
Program Report Tool-- 18 1 8
Initial.
Work Plan Tool--Annual 55 1 3
Reporting.
Program Report Tool-- 55 1 3
Annual Reporting.
----------------------------------------------------------------------------------------------------------------
Leroy A. Richardson,
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. 2016-12053 Filed 5-20-16; 8:45 am]
BILLING CODE 4163-18-P
