Proposed Data Collection Submitted for Public Comment and Recommendations, 36539-36540 [2015-15550]
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Federal Register / Vol. 80, No. 122 / Thursday, June 25, 2015 / Notices
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Dated: June 22, 2015.
Federal Deposit Insurance Corporation.
Robert E. Feldman,
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BILLING CODE 6714–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–0571]; [Docket No. CDC–2015–
0015]
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 the collection of Minimum
Data Elements (MDE) for the National
Breast and Cervical Cancer Early
Detection Program (NBCCEDP). CDC
collects information about the cancer
screening services provided through the
NBCCEDP to support program
management.
SUMMARY:
Written comments must be
received on or before August 24, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0015 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
asabaliauskas on DSK5VPTVN1PROD with NOTICES
VerDate Sep<11>2014
16:37 Jun 24, 2015
Jkt 235001
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
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
FOR FURTHER INFORMATION CONTACT:
[FR Doc. 2015–15608 Filed 6–24–15; 8:45 am]
DATES:
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
36539
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
Minimum Data Elements (MDE) for
the National Breast and Cervical Cancer
Early Detection Program (NBCCEDP)
(OMB No. 0920–0571, exp. 10/31/
2015)—Extension—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Many cancer-related deaths in women
could be avoided by increased
utilization of appropriate screening and
early detection tests for breast and
cervical cancer. Mammography is
extremely valuable as an early detection
tool because it can detect breast cancer
well before the woman can feel the
lump, when the cancer is still in an
early and more treatable stage.
Similarly, a substantial proportion of
cervical cancer-related deaths could be
prevented through the detection and
treatment of precancerous lesions. The
Papanicolaou (Pap) test is the primary
method of detecting both precancerous
cervical lesions as well as invasive
cervical cancer. Mammography and Pap
tests are underused by women who have
no source or no regular source of health
care and women without health
insurance.
Despite the availability and increased
use of effective screening and early
detection tests for breast and cervical
cancers, the American Cancer Society
(ACS) estimates that 231,840 new cases
of invasive breast cancer will be
diagnosed among women in 2015, and
40,290 women will die of this disease.
The ACS also estimates that 12,900 new
cases of invasive cervical cancer will be
diagnosed in 2015, and 4,100 women
will die of this disease.
The CDC’s National Breast and
Cervical Cancer Early Detection Program
(NBCCEDP) provides screening services
to underserved women through
cooperative agreements with 50 States,
the District of Columbia, 5 U.S.
Territories, and 11 American Indian/
Alaska Native tribal programs. The
program was established in response to
the Breast and Cervical Cancer Mortality
Prevention Act of 1990. Screening
services include clinical breast
examinations, mammograms and Pap
tests, as well as timely and adequate
diagnostic testing for abnormal results,
E:\FR\FM\25JNN1.SGM
25JNN1
36540
Federal Register / Vol. 80, No. 122 / Thursday, June 25, 2015 / Notices
and referrals to treatment for cancers
detected. NBCCEDP awardees collect
patient-level screening and tracking data
to manage the program and clinical
services. A de-identified subset of data
on patient demographics, screening tests
and outcomes are reported by each
awardee to CDC twice per year.
CDC plans to request OMB approval
to collect MDE information for an
additional three years. There are no
changes to the currently approved
minimum data elements, electronic data
collection procedures, or the estimated
burden. Because NBCCEDP awardees
already collect and aggregate data at the
state, territory and tribal level, the
additional burden of submitting data to
CDC will be modest. CDC will use the
information to monitor and evaluate
NBCCEDP awardees; improve the
availability and quality of screening and
diagnostic services for underserved
women; develop outreach strategies for
women who are never or rarely screened
for breast and cervical cancer; report
program results to stakeholders
including Congress and other legislative
authorities; and inform program
planning and management.
There are no costs to respondents
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hrs.)
NBCCEDP Grantees ........................
Minimum Data Elements ..................
67
2
4
536
Total ...........................................
...........................................................
........................
........................
........................
536
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. 2015–15550 Filed 6–24–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–15–0840; Docket No. CDC–2015–
0046]
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 extension of the
‘‘Formative Research and Tool
Development’’ information collection.
Project activities are designed to allow
CDC’s National Center for HIV/AIDS,
Viral Hepatitis, STD, and TB Prevention
(NCHHSTP) to conduct formative
research information collection
asabaliauskas on DSK5VPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
16:37 Jun 24, 2015
Jkt 235001
activities used to inform many aspects
of surveillance, communications, health
promotion, and research project
development for NCHHSTP’s four
priority diseases (HIV/AIDS), sexually
transmitted diseases/infections (STD/
STI), viral hepatitis, tuberculosis
elimination (TB), and school and
adolescent health (DASH).
DATES: Written comments must be
received on or before August 24, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0046 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,
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
Total burden
(in hrs.)
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
E:\FR\FM\25JNN1.SGM
25JNN1
]]>Agencies
[Federal Register Volume 80, Number 122 (Thursday, June 25, 2015)]
[Notices]
[Pages 36539-36540]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-15550]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-0571]; [Docket No. CDC-2015-0015]
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 the collection of
Minimum Data Elements (MDE) for the National Breast and Cervical Cancer
Early Detection Program (NBCCEDP). CDC collects information about the
cancer screening services provided through the NBCCEDP to support
program management.
DATES: Written comments must be received on or before August 24, 2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0015 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
Minimum Data Elements (MDE) for the National Breast and Cervical
Cancer Early Detection Program (NBCCEDP) (OMB No. 0920-0571, exp. 10/
31/2015)--Extension--National Center for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
Many cancer-related deaths in women could be avoided by increased
utilization of appropriate screening and early detection tests for
breast and cervical cancer. Mammography is extremely valuable as an
early detection tool because it can detect breast cancer well before
the woman can feel the lump, when the cancer is still in an early and
more treatable stage. Similarly, a substantial proportion of cervical
cancer-related deaths could be prevented through the detection and
treatment of precancerous lesions. The Papanicolaou (Pap) test is the
primary method of detecting both precancerous cervical lesions as well
as invasive cervical cancer. Mammography and Pap tests are underused by
women who have no source or no regular source of health care and women
without health insurance.
Despite the availability and increased use of effective screening
and early detection tests for breast and cervical cancers, the American
Cancer Society (ACS) estimates that 231,840 new cases of invasive
breast cancer will be diagnosed among women in 2015, and 40,290 women
will die of this disease. The ACS also estimates that 12,900 new cases
of invasive cervical cancer will be diagnosed in 2015, and 4,100 women
will die of this disease.
The CDC's National Breast and Cervical Cancer Early Detection
Program (NBCCEDP) provides screening services to underserved women
through cooperative agreements with 50 States, the District of
Columbia, 5 U.S. Territories, and 11 American Indian/Alaska Native
tribal programs. The program was established in response to the Breast
and Cervical Cancer Mortality Prevention Act of 1990. Screening
services include clinical breast examinations, mammograms and Pap
tests, as well as timely and adequate diagnostic testing for abnormal
results,
[[Page 36540]]
and referrals to treatment for cancers detected. NBCCEDP awardees
collect patient-level screening and tracking data to manage the program
and clinical services. A de-identified subset of data on patient
demographics, screening tests and outcomes are reported by each awardee
to CDC twice per year.
CDC plans to request OMB approval to collect MDE information for an
additional three years. There are no changes to the currently approved
minimum data elements, electronic data collection procedures, or the
estimated burden. Because NBCCEDP awardees already collect and
aggregate data at the state, territory and tribal level, the additional
burden of submitting data to CDC will be modest. CDC will use the
information to monitor and evaluate NBCCEDP awardees; improve the
availability and quality of screening and diagnostic services for
underserved women; develop outreach strategies for women who are never
or rarely screened for breast and cervical cancer; report program
results to stakeholders including Congress and other legislative
authorities; and inform program planning and management.
There are no costs 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 Total burden
respondents respondent (in hrs.) (in hrs.)
----------------------------------------------------------------------------------------------------------------
NBCCEDP Grantees............ Minimum Data 67 2 4 536
Elements.
------------------------------------------------------------------
Total................... ............... ............... ............... ............... 536
----------------------------------------------------------------------------------------------------------------
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. 2015-15550 Filed 6-24-15; 8:45 am]
BILLING CODE 4163-18-P
