Proposed Data Collection Submitted for Public Comment and Recommendations, 66308-66309 [2021-25448]
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66308
Federal Register / Vol. 86, No. 222 / Monday, November 22, 2021 / Notices
the services delivered in the Learning
Community.
No other federal agency collects these
types of national HIV prevention
capacity building data. Respondents
will provide information electronically
through the online Registration Form
and Post-Participation Survey. The
number of respondents is calculated
based on an expected number of CBO
managers at CDC-funded organizations,
given the previous number of
organizations funded by CDC. We
estimate 270 CBO managers will
complete the Registration Form and the
Post-Participation Survey, and 135 will
provide responses to the SemiStructured Interview, annually. The
total annualized burden is 89 hours.
There are no other costs to respondents
other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
CBO Managers ...............................................
CBO Managers ...............................................
CBO Managers ...............................................
Registration Form ...........................................
Post Participation Survey ...............................
Semi-Structured Zoom Interview ...................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–25446 Filed 11–19–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–0469; Docket No. CDC–2021–
0123]
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.
This information collection provides
useful data on cancer incidence and
trends.
SUMMARY:
jspears on DSK121TN23PROD with NOTICES1
Number of
respondents
Type of respondent
CDC must receive written
comments on or before January 21,
2022.
DATES:
You may submit comments,
identified by Docket No. CDC–2021–
0123 by any of the following methods:
ADDRESSES:
VerDate Sep<11>2014
18:30 Nov 19, 2021
Jkt 256001
• 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 H21–8, 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 Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, 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.
The OMB is particularly interested in
comments that will help:
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
270
270
135
1
1
1
Average
burden per
response
(in hours)
3/60
9/60
15/60
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;
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; and
5. Assess information collection costs.
Proposed Project
National Program of Cancer Registries
Cancer Surveillance System (OMB
Control No. 0920–0469, Exp. 12/31/
2022)—Revision—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 2018, the most recent year for
which complete incidence information
is available, almost 600,000 people died
of cancer and more than 1.7 million
were diagnosed with cancer. It is
estimated that 16.3 million Americans
are currently alive with a history of
cancer. In the United States, state/
territory-based central cancer registries
(CCR) are the only method for
systematically collecting and reporting
population-based information about
cancer incidence and outcomes such as
survival. These data are used to measure
the changing incidence and burden of
E:\FR\FM\22NON1.SGM
22NON1
66309
Federal Register / Vol. 86, No. 222 / Monday, November 22, 2021 / Notices
each cancer; identify populations at
increased or increasing risk; target
preventive measures; and measure the
success or failure of cancer control
efforts in the United States.
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 No. 0920–0469, Exp.
12/31/2022). 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. No changes to the
total estimated annualized burden hours
or number of respondents are
anticipated.
The NPCR CSS allows CDC to collect,
aggregate, evaluate, and disseminate
cancer incidence data at the national
level. The NPCR CSS is the primary
submitted in January, is a preliminary
report consisting of one year of data for
the most recent year of data available.
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., 2018). 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. CDC requests
approval for an estimated 200 annual
burden hours. There are no costs to
respondents other than their time.
source of information for the United
States Cancer Statistics (USCS), which
CDC has published annually since 2002.
The latest USCS report, published in
2021, provided cancer statistics for 99%
of the U.S. 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,
ESTIMATED ANNUALIZED BURDEN HOURS
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. 2021–25448 Filed 11–19–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–22AQ; Docket No. CDC–2021–
0122]
jspears on DSK121TN23PROD with NOTICES1
Average
burden per
response
(in hours)
Number of
responses per
respondent
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).
AGENCY:
ACTION:
Notice with comment period.
VerDate Sep<11>2014
18:30 Nov 19, 2021
Jkt 256001
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 ‘‘Requirement for Airlines and
Operators to Collect and Transmit
Designated Information for Passengers
and Crew Arriving Into the United
States; Requirement for Passengers to
Provide Designated Information,’’ which
will provide CDC with the ability to
collect traveler contact information from
passengers and airlines to facilitate any
necessary public health follow-up.
SUMMARY:
CDC must receive written
comments on or before January 21,
2022.
DATES:
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
You may submit comments,
identified by Docket No. CDC–2021–
0122 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffery M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, 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 Jeffery M. Zirger, of
ADDRESSES:
E:\FR\FM\22NON1.SGM
22NON1
]]>Agencies
[Federal Register Volume 86, Number 222 (Monday, November 22, 2021)]
[Notices]
[Pages 66308-66309]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-25448]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-22-0469; Docket No. CDC-2021-0123]
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. This information collection
provides useful data on cancer incidence and trends.
DATES: CDC must receive written comments on or before January 21, 2022.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0123 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 H21-8, 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 Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS H21-8, 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;
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; and
5. Assess information collection costs.
Proposed Project
National Program of Cancer Registries Cancer Surveillance System
(OMB Control No. 0920-0469, Exp. 12/31/2022)--Revision--National Center
for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention (CDC).
Background and Brief Description
In 2018, the most recent year for which complete incidence
information is available, almost 600,000 people died of cancer and more
than 1.7 million were diagnosed with cancer. It is estimated that 16.3
million Americans are currently alive with a history of cancer. In the
United States, state/territory-based central cancer registries (CCR)
are the only method for systematically collecting and reporting
population-based information about cancer incidence and outcomes such
as survival. These data are used to measure the changing incidence and
burden of
[[Page 66309]]
each cancer; identify populations at increased or increasing risk;
target preventive measures; and measure the success or failure of
cancer control efforts in the United States.
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 No. 0920-0469, Exp. 12/31/2022). 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. No changes to the total estimated
annualized burden hours or number of respondents are anticipated.
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 the United States Cancer
Statistics (USCS), which CDC has published annually since 2002. The
latest USCS report, published in 2021, provided cancer statistics for
99% of the U.S. 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 data
available. 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., 2018). 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. CDC
requests approval for an estimated 200 annual burden hours. 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 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. 2021-25448 Filed 11-19-21; 8:45 am]
BILLING CODE 4163-18-P
