Proposed Data Collection Submitted for Public Comment and Recommendations, 44965-44966 [2015-18456]
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44965
Federal Register / Vol. 80, No. 144 / Tuesday, July 28, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Safety/health Mine Representative .................
Safety/health Mine Manager ...........................
Mine Manager Recruitment Script .................
HSMS Interview/Focus Group Protocol .........
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. 2015–18455 Filed 7–27–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–15AUK: Docket No. CDC–2015–
0058]
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
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 a proposed information
collection entitled Monitoring and
Reporting System for the Prescription
Drug Overdose Prevention for States
Cooperative Agreement. CDC will use
the information collected to monitor
cooperative agreement awardees and to
identify challenges to program
implementation and achievement of
outcomes.
DATES: Written comments must be
received on or before September 28,
2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0058 by any of the following methods:
Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson,
Information Collection Review Office,
asabaliauskas on DSK5VPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
19:17 Jul 27, 2015
Jkt 235001
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.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact 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
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 OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
8
34
Average
burden per
response
(in hours)
1
1
5/60
55/60
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Monitoring and Reporting System for
the Prescription Drug Overdose
Prevention for States Cooperative
agreement—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Drug overdose is the leading cause of
injury death in the United States.
Opioid-prescribing behaviors are
associated with an increased risk for
morbidity and mortality. While opioid
pain relievers can play an important
role in the management of some types
of pain, the overprescribing of these
powerful drugs has fueled a national
epidemic of prescription drug abuse and
overdose. To reverse this complex
epidemic and prevent future overdose,
abuse, and misuse, the Centers for
Disease Control and Prevention (CDC)
provides support to states to improve
surveillance. Support and guidance for
these programs have been provided
through cooperative agreement funding
and technical assistance administered
by CDC’s National Center for Injury
Prevention and Control (NCIPC).
E:\FR\FM\28JYN1.SGM
28JYN1
44966
Federal Register / Vol. 80, No. 144 / Tuesday, July 28, 2015 / Notices
The goal of this ICR is to collect
information from awardees funded
under the Prescription Drug Overdose
Prevention for States (CDC–RFA–CE15–
1501) cooperative agreement, for
program monitoring and improvement
among funded state health departments.
Information to be collected will
provide crucial data for program
performance monitoring and budget
tracking, and provide CDC with the
capacity to respond in a timely manner
to requests for information about the
program from the Department of Health
and Human Services (HHS), the White
House, Congress, and other sources.
Awardees will report progress and
activity information to CDC on an
annual schedule using an Excel-based
fillable electronic templates, prepopulated to the extent possible by CDC
information only needs to be updated
for each annual report. The same
instruments will be used for all
information collection and reporting.
CDC will use the information
collected to monitor each awardee’s
progress and to identify facilitators and
challenges to program implementation
and achievement of outcomes.
Monitoring allows CDC to determine
whether an awardee is meeting
performance and budget goals and to
make adjustments in the type and level
of technical assistance provided to
them, as needed, to support attainment
of their performance measures.
OMB approval is requested for three
years. Participation in the information
collection is required as a condition of
funding. There are no costs to
respondents other than their time.
staff, to be submitted via Grant
Solutions. Each awardee will submit an
Annual reporting Progress Report Tool.
The estimated burden per response is 4
hours for each Annual reporting
Progress Report Tool. In addition, each
awardee will submit an Annual
reporting Evaluation Plan Tool. The
estimated burden per response is 3
hours for each Annual reporting
Evaluation Plan Tool.
In Year 1, each awardee will have
additional burden related to initial
collection of the reporting tools. Initial
Collection Annual Progress Report Tool
is estimated to be 20 hours per response,
Initial population of the tools is a onetime activity which is annualized over
the 3 years of the information collection
request. After completing the initial
population of the tools, pertinent
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Type of respondents
Form name
State and Territorial Health Department Program Awardees.
Initial Collection Annual Progress
Report Tool.
Annual reporting—Progress Report
Tool.
Annual reporting Evaluation Plan
Tool.
16
1
20
320
16
1
4
64
16
1
4
64
...........................................................
........................
........................
........................
448
Total ...........................................
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. 2015–18456 Filed 7–27–15; 8:45 am]
BILLING CODE 4163–18P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–15–15UJ]
asabaliauskas on DSK5VPTVN1PROD with NOTICES
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
VerDate Sep<11>2014
19:17 Jul 27, 2015
Jkt 235001
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
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
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
Examining How Local Health
Departments Can Leverage Age-Friendly
Cities Initiatives to Build Resilience in
Elderly Populations—New—Office of
Public Health Preparedness and
Response, Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Despite considerable progress in
efforts to define and build community
resilience (CR), critical gaps remain in
addressing the needs of older adults (age
60+), which is expected to rise to 25%
by 2050. Age Friendly Initiatives (AFIs),
including Senior Villages (SV) represent
a promising strategy for U.S.
communities and cities to support older
adults aging in place, and could
potentially build CR. However, few AFIs
have wholly incorporated the critical
element of emergency preparedness and
E:\FR\FM\28JYN1.SGM
28JYN1
]]>Agencies
[Federal Register Volume 80, Number 144 (Tuesday, July 28, 2015)]
[Notices]
[Pages 44965-44966]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-18456]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-15AUK: Docket No. CDC-2015-0058]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts to reduce public 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 a proposed
information collection entitled Monitoring and Reporting System for the
Prescription Drug Overdose Prevention for States Cooperative Agreement.
CDC will use the information collected to monitor cooperative agreement
awardees and to identify challenges to program implementation and
achievement of outcomes.
DATES: Written comments must be received on or before September 28,
2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0058 by any of the following methods:
Federal eRulemaking Portal: Regulation.gov. Follow the instructions
for submitting comments.
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.
Please note: All public comment should be submitted through the
Federal eRulemaking portal (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 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 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 OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; (d) ways to
minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services
to provide information. Burden means the total time, effort, or
financial resources expended by persons to generate, maintain, retain,
disclose or provide information to or for a Federal agency. This
includes the time needed to review instructions; to develop, acquire,
install and utilize technology and systems for the purpose of
collecting, validating and verifying information, processing and
maintaining information, and disclosing and providing information; to
train personnel and to be able to respond to a collection of
information, to search data sources, to complete and review the
collection of information; and to transmit or otherwise disclose the
information.
Proposed Project
Monitoring and Reporting System for the Prescription Drug Overdose
Prevention for States Cooperative agreement--New--National Center for
Injury Prevention and Control (NCIPC), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Drug overdose is the leading cause of injury death in the United
States. Opioid-prescribing behaviors are associated with an increased
risk for morbidity and mortality. While opioid pain relievers can play
an important role in the management of some types of pain, the
overprescribing of these powerful drugs has fueled a national epidemic
of prescription drug abuse and overdose. To reverse this complex
epidemic and prevent future overdose, abuse, and misuse, the Centers
for Disease Control and Prevention (CDC) provides support to states to
improve surveillance. Support and guidance for these programs have been
provided through cooperative agreement funding and technical assistance
administered by CDC's National Center for Injury Prevention and Control
(NCIPC).
[[Page 44966]]
The goal of this ICR is to collect information from awardees funded
under the Prescription Drug Overdose Prevention for States (CDC-RFA-
CE15-1501) cooperative agreement, for program monitoring and
improvement among funded state health departments.
Information to be collected will provide crucial data for program
performance monitoring and budget tracking, and provide CDC with the
capacity to respond in a timely manner to requests for information
about the program from the Department of Health and Human Services
(HHS), the White House, Congress, and other sources. Awardees will
report progress and activity information to CDC on an annual schedule
using an Excel-based fillable electronic templates, pre-populated to
the extent possible by CDC staff, to be submitted via Grant Solutions.
Each awardee will submit an Annual reporting Progress Report Tool. The
estimated burden per response is 4 hours for each Annual reporting
Progress Report Tool. In addition, each awardee will submit an Annual
reporting Evaluation Plan Tool. The estimated burden per response is 3
hours for each Annual reporting Evaluation Plan Tool.
In Year 1, each awardee will have additional burden related to
initial collection of the reporting tools. Initial Collection Annual
Progress Report Tool is estimated to be 20 hours per response, Initial
population of the tools is a one-time activity which is annualized over
the 3 years of the information collection request. After completing the
initial population of the tools, pertinent information only needs to be
updated for each annual report. The same instruments will be used for
all information collection and reporting.
CDC will use the information collected to monitor each awardee's
progress and to identify facilitators and challenges to program
implementation and achievement of outcomes. Monitoring allows CDC to
determine whether an awardee is meeting performance and budget goals
and to make adjustments in the type and level of technical assistance
provided to them, as needed, to support attainment of their performance
measures.
OMB approval is requested for three years. Participation in the
information collection is required as a condition of funding. There are
no costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
State and Territorial Health Initial 16 1 20 320
Department Program Awardees. Collection
Annual Progress
Report Tool.
Annual 16 1 4 64
reporting--Prog
ress Report
Tool.
Annual reporting 16 1 4 64
Evaluation Plan
Tool.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 448
----------------------------------------------------------------------------------------------------------------
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. 2015-18456 Filed 7-27-15; 8:45 am]
BILLING CODE 4163-18P
