Proposed Data Collection Submitted for Public Comment and Recommendations, 25056-25057 [2019-11216]
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Federal Register / Vol. 84, No. 104 / Thursday, May 30, 2019 / Notices
collection from its current focus on
opioid overdose deaths to a broader
focus on drug overdose deaths, (3)
account for increasing data collection
burden related to large increases in drug
overdose deaths, (4) increase the
timeliness of data reporting to a 6month time lag, and (5) update the web-
prevention strategies at both the state
and national levels. Improve
identification and response to changes
in fatal unintentional and undetermined
intent drug-related overdose trends at
the local, state, and national level. There
are no costs to respondents other than
their time.
based system to improve performance,
functionality, and accessibility as well
as add data elements to the State
Unintentional Drug Overdose Reporting
System (SUDORS) module to capture
more detailed information. This
information will help develop, inform,
and assess the progress of drug overdose
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Total
burden hours
(in hours)
Form name
Public agencies .................................
Retrieving and refile records ............
52
1263
30/60
32,838
Total ...........................................
...........................................................
........................
........................
........................
32,838
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–11215 Filed 5–29–19; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–19–0469; Docket No. CDC–2019–
0031]
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 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 and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled National Program of Cancer
Registries Cancer Surveillance System
(NPCR CSS). The NPCR CSS provides
useful data on cancer incidence and
trends.
SUMMARY:
jbell on DSK3GLQ082PROD with NOTICES
Total number
of responses
per
respondent
Number of
respondents
Type of respondent
CDC must receive written
comments on or before July 29, 2019.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0031 by any of the following methods:
DATES:
VerDate Sep<11>2014
18:08 May 29, 2019
Jkt 247001
• Federal eRulemaking Portal:
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–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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 Leroy A.
Richardson, 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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
PO 00000
Frm 00029
Fmt 4703
Sfmt 4703
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; and
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.
5. Assess information collection costs.
Proposed Project
National Program of Cancer Registries
Cancer Surveillance System (OMB No.
0920–0469, Exp. 6/30/2019)—
Revision—National Center for Chronic
Disease Prevention and health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 2015, the most recent year for
which complete information is
available, almost 596,000 people died of
cancer and more than 1.6 million were
diagnosed with cancer. It is estimated
that 15.8 million Americans are
currently alive with a history of cancer.
In the U.S., state/territory-based cancer
registries are the only method for
systematically collecting and reporting
population based information about
cancer incidence and outcomes such as
E:\FR\FM\30MYN1.SGM
30MYN1
25057
Federal Register / Vol. 84, No. 104 / Thursday, May 30, 2019 / Notices
survival. These data are used to measure
the changing incidence and burden of
each cancer; identify populations at
increased or increasing risk; target
preventive measures; and measure the
success or failure of cancer control
efforts in the U.S.
In 1992, Congress passed the Cancer
Registries Amendment Act which
established the National Program of
Cancer Registries (NPCR). The NPCR
provides support for state/territorybased cancer registries that collect,
manage and analyze data about cancer
cases. The state/territory-based cancer
registries report information to CDC
through the National Program of Cancer
Registries Cancer Surveillance System
(NPCR CSS), (OMB Control No. 0920–
0469). CDC plans to request OMB
approval to continue collecting this
information for three years. Data
definitions will be updated to reflect
changes in national standards for cancer
diagnosis and coding. The number of
respondents has been updated to reflect
the increased number of states/
territories supported by CDC, but the
burden per respondent will not change.
The NPCR CSS allows CDC to collect,
aggregate, evaluate, and disseminate
The first NPCR CSS Standard file,
submitted in January, is a preliminary
report consisting of one year of data for
the most recent year of available data.
CDC evaluates the preliminary data for
completeness and quality and provides
a report back to the CCR. The second
NPCR CSS Standard file, submitted by
November, contains cumulative cancer
incidence data from the first diagnosis
year for which the cancer registry
collected data with the assistance of
NPCR funds (e.g., 1995) through 12
months past the close of the most recent
diagnosis year (e.g., 2016). The
cumulative file is used for analysis and
reporting.
The burden for each file transmission
is estimated at two hours per response.
Because cancer incidence data are
already collected and aggregated at the
state level the additional burden of
reporting the information to CDC is
small. All information is transmitted to
CDC electronically. Participation is
required as a condition of the
cooperative agreement with CDC. The
total estimated annual burden hours is
200. There are no costs to respondents
except their time.
cancer incidence data at the national
level. The NPCR CSS is the primary
source of information for United States
Cancer Statistics (USCS), which CDC
has published annually since 2002. The
latest USCS report published in 2018
provided cancer statistics for 100% of
the United States population from all
cancer registries in the United States.
Prior to the publication of USCS, cancer
incidence data at the national level were
available for only 14% of the population
of the United States.
The NPCR CSS also allows CDC to
monitor cancer trends over time,
describe geographic variation in cancer
incidence throughout the country, and
provide incidence data on racial/ethnic
populations and rare cancers. These
activities and analyses further support
CDC’s planning and evaluation efforts
for state and national cancer control and
prevention. In addition, datasets can be
made available for secondary analysis.
Respondents are NPCR-supported
central cancer registries (CCR) in 46 U.S.
states, three territories, and the District
of Columbia. Fifty CCRs submit data
elements specified for the Standard
NPCR CSS Report. Each CCR is asked to
transmit two data files to CDC per year.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden
per response
(in hours)
Number of
responses per
respondent
Total burden
(in hours)
Form name
Central Cancer Registries in States,
Territories, and the District of Columbia.
Standard NPCR CSS Report ...........
50
2
2
200
Total ...........................................
...........................................................
........................
........................
........................
200
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–11216 Filed 5–29–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–19–19AWX; Docket No. CDC–2019–
0042]
jbell on DSK3GLQ082PROD with NOTICES
Number of
respondents
Type of respondents
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:
VerDate Sep<11>2014
18:08 May 29, 2019
Jkt 247001
The Centers for Disease
Control and Prevention (CDC), 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 and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled WISEWOMAN National Program
Evaluation. The goal of the study is to
assess the implementation of the
WISEWOMAN program under the
current cooperative agreement and
measure the effect of the program on
individual-, organizational-, and
community-level outcomes.
SUMMARY:
CDC must receive written
comments on or before July 29, 2019.
DATES:
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
You may submit comments,
identified by Docket No. CDC–2019–
0042 by any of the following methods:
• Federal eRulemaking Portal:
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–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
ADDRESSES:
Please note: Submit all comments 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
FOR FURTHER INFORMATION CONTACT:
E:\FR\FM\30MYN1.SGM
30MYN1
]]>Agencies
[Federal Register Volume 84, Number 104 (Thursday, May 30, 2019)]
[Notices]
[Pages 25056-25057]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-11216]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-19-0469; Docket No. CDC-2019-0031]
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 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 and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled National Program of Cancer
Registries Cancer Surveillance System (NPCR CSS). The NPCR CSS provides
useful data on cancer incidence and trends.
DATES: CDC must receive written comments on or before July 29, 2019.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2019-
0031 by any of the following methods:
Federal eRulemaking Portal: 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-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments 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 Leroy A. Richardson, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
[email protected].
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; and
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.
5. Assess information collection costs.
Proposed Project
National Program of Cancer Registries Cancer Surveillance System
(OMB No. 0920-0469, Exp. 6/30/2019)--Revision--National Center for
Chronic Disease Prevention and health Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 2015, the most recent year for which complete information is
available, almost 596,000 people died of cancer and more than 1.6
million were diagnosed with cancer. It is estimated that 15.8 million
Americans are currently alive with a history of cancer. In the U.S.,
state/territory-based cancer registries are the only method for
systematically collecting and reporting population based information
about cancer incidence and outcomes such as
[[Page 25057]]
survival. These data are used to measure the changing incidence and
burden of each cancer; identify populations at increased or increasing
risk; target preventive measures; and measure the success or failure of
cancer control efforts in the U.S.
In 1992, Congress passed the Cancer Registries Amendment Act which
established the National Program of Cancer Registries (NPCR). The NPCR
provides support for state/territory-based cancer registries that
collect, manage and analyze data about cancer cases. The state/
territory-based cancer registries report information to CDC through the
National Program of Cancer Registries Cancer Surveillance System (NPCR
CSS), (OMB Control No. 0920-0469). CDC plans to request OMB approval to
continue collecting this information for three years. Data definitions
will be updated to reflect changes in national standards for cancer
diagnosis and coding. The number of respondents has been updated to
reflect the increased number of states/territories supported by CDC,
but the burden per respondent will not change.
The NPCR CSS allows CDC to collect, aggregate, evaluate, and
disseminate cancer incidence data at the national level. The NPCR CSS
is the primary source of information for United States Cancer
Statistics (USCS), which CDC has published annually since 2002. The
latest USCS report published in 2018 provided cancer statistics for
100% of the United States population from all cancer registries in the
United States. Prior to the publication of USCS, cancer incidence data
at the national level were available for only 14% of the population of
the United States.
The NPCR CSS also allows CDC to monitor cancer trends over time,
describe geographic variation in cancer incidence throughout the
country, and provide incidence data on racial/ethnic populations and
rare cancers. These activities and analyses further support CDC's
planning and evaluation efforts for state and national cancer control
and prevention. In addition, datasets can be made available for
secondary analysis.
Respondents are NPCR-supported central cancer registries (CCR) in
46 U.S. states, three territories, and the District of Columbia. Fifty
CCRs submit data elements specified for the Standard NPCR CSS Report.
Each CCR is asked to transmit two data files to CDC per year. The first
NPCR CSS Standard file, submitted in January, is a preliminary report
consisting of one year of data for the most recent year of available
data. CDC evaluates the preliminary data for completeness and quality
and provides a report back to the CCR. The second NPCR CSS Standard
file, submitted by November, contains cumulative cancer incidence data
from the first diagnosis year for which the cancer registry collected
data with the assistance of NPCR funds (e.g., 1995) through 12 months
past the close of the most recent diagnosis year (e.g., 2016). The
cumulative file is used for analysis and reporting.
The burden for each file transmission is estimated at two hours per
response. Because cancer incidence data are already collected and
aggregated at the state level the additional burden of reporting the
information to CDC is small. All information is transmitted to CDC
electronically. Participation is required as a condition of the
cooperative agreement with CDC. The total estimated annual burden hours
is 200. There are no costs to respondents except 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 hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Central Cancer Registries in Standard NPCR 50 2 2 200
States, Territories, and the CSS Report.
District of Columbia.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 200
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-11216 Filed 5-29-19; 8:45 am]
BILLING CODE 4163-18-P
