Proposed Data Collection Submitted for Public Comment and Recommendations, 50124-50125 [2021-19163]
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50124
Federal Register / Vol. 86, No. 170 / Tuesday, September 7, 2021 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–19162 Filed 9–3–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–21–1092; Docket No. CDC–2021–
0091]
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 Sudden Death in the Young
(SDY). The goal of the SDY Case
Registry is to improve and standardize
the ascertainment of deaths so that
funded jurisdictions can better
understand the incidence and risk
factors for sudden death in youth. Per
CDC’s cooperative agreement,
respondents agree to compile a defined
set of SDY information about a defined
subset of child deaths through the
jurisdiction/state’s existing CDR
program.
DATES: CDC must receive written
comments on or before November 8,
2021.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2021–
0091 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
sradovich on DSKJLST7X2PROD with NOTICES
SUMMARY:
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.
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 Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7118; 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:
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
Proposed Project
Sudden Death in the Young (SDY)
(OMB Control No. 0920–1092, Exp. 04/
30/2022)—Extension—National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPHP), Centers
for Disease Control and Prevention
(CDC)
Background and Brief Description
Estimates of the annual incidence of
sudden death in the young (SDY) vary
broadly due to differences in case
definitions, inconsistencies in
classifying cause of death (on death
certificates), study populations, and
case ascertainment. To address the need
for improved estimates of SDY
incidence, and its epidemiology based
on uniform cases definitions, CDC, in
collaboration with NIH’s National Heart,
Lung, and Blood Institute (NHLBI) and
National Institute of Neurological
Disorders and Stroke (NINDS),
implemented the SDY Case Registry in
2015. To meet the ongoing need to
produce accurate and uniform
information, CDC and NIH continued
the SDY Case Registry in 2018 with 13
awardees through a CDC-based
cooperative agreement program (DP18–
1806).
CDC awardees agree to compile a
defined set of SDY information about a
defined subset of child deaths through
the jurisdiction/state’s existing CDR
program. Each of the 13 CDC-funded
jurisdiction/state awardees will, on
average, review and enter data on 55 of
720 cases each year. Additionally, based
on historical program information, it is
estimated that approximately half (360)
of the 720 estimated SDY cases each
year will be recommended for advanced
clinical review by a team of three
medical experts.
OMB approval is requested for three
years. The total estimated annual
burden is 511 hours. There are no costs
to respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
State health personnel ..........................................
SDY Module I ...............
VerDate Sep<11>2014
00:30 Sep 04, 2021
Jkt 253001
PO 00000
Frm 00113
Fmt 4703
I
Sfmt 4703
13
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Type of respondent
I
U:\07SEN1.SGM
55
07SEN1
I
10/60
Total burden
hours
119
50125
Federal Register / Vol. 86, No. 170 / Tuesday, September 7, 2021 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Average
burden per
response
(in hours)
Total burden
hours
Form name
Medical Expert ......................................................
State Health Personnel .........................................
Advanced Review .........
SDY Module N .............
39
13
28
55
15/60
10/60
273
119
Total hours .....................................................
.......................................
........................
........................
........................
511
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–19163 Filed 9–3–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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 Wastewater Surveillance
System for COVID–19. The proposed
information collection project aims to
collect SARS–CoV–2 wastewater and
associated sewershed-level case data
from participating jurisdictions in the
United States to inform COVID–19
prevention and control efforts.
DATES: CDC must receive written
comments on or before November 8,
2021.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2021–
0090 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
SUMMARY:
VerDate Sep<11>2014
00:30 Sep 04, 2021
Jkt 253001
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.
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–
D74, Atlanta, Georgia 30329; phone:
404–639–7118; Email: omb@cdc.gov.
FOR FURTHER INFORMATION CONTACT:
[60Day–21–21HT; Docket No. CDC–2021–
0090]
sradovich on DSKJLST7X2PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Type of respondent
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;
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00114
Fmt 4703
Sfmt 4703
U:\07SEN1.SGM
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 Wastewater Surveillance
System for COVID–19—New—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
The COVID–19 pandemic has
demonstrated the need for timely,
actionable surveillance data to inform
prevention and control activities. The
genetic material of SARS–CoV–2, the
virus that causes COVID–19, has been
detected in the feces of infected
individuals, regardless of their symptom
status. Therefore, sampling and testing
wastewater provides a means to obtain
an assessment of SARS–CoV–2 infection
trends in the community independent of
health care seeking, or other clinical
indicators.
The Waterborne Disease Prevention
Branch (WDPB) in the Division of
Foodborne, Waterborne, and
Environmental Diseases works to
prevent domestic and global water,
sanitation, and hygiene related disease.
In support of the Centers for Disease
Control and Prevention (CDC) COVID–
19 response, WDPB established the
National Wastewater Surveillance
System (NWSS). NWSS serves as a
public health tool to provide
environmental surveillance of SARS–
CoV–2 infections. Wastewater data have
provided impactful information to local
public health authorities, whether to
confirm trends observed in testing or
hospitalization rates, or to assert the
need for increased testing or healthcare
resources. NWSS has supported
07SEN1
]]>Agencies
[Federal Register Volume 86, Number 170 (Tuesday, September 7, 2021)]
[Notices]
[Pages 50124-50125]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-19163]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-21-1092; Docket No. CDC-2021-0091]
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 Sudden Death in the Young (SDY).
The goal of the SDY Case Registry is to improve and standardize the
ascertainment of deaths so that funded jurisdictions can better
understand the incidence and risk factors for sudden death in youth.
Per CDC's cooperative agreement, respondents agree to compile a defined
set of SDY information about a defined subset of child deaths through
the jurisdiction/state's existing CDR program.
DATES: CDC must receive written comments on or before November 8, 2021.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0091 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 Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7118; 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
Sudden Death in the Young (SDY) (OMB Control No. 0920-1092, Exp.
04/30/2022)--Extension--National Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP), Centers for Disease Control and
Prevention (CDC)
Background and Brief Description
Estimates of the annual incidence of sudden death in the young
(SDY) vary broadly due to differences in case definitions,
inconsistencies in classifying cause of death (on death certificates),
study populations, and case ascertainment. To address the need for
improved estimates of SDY incidence, and its epidemiology based on
uniform cases definitions, CDC, in collaboration with NIH's National
Heart, Lung, and Blood Institute (NHLBI) and National Institute of
Neurological Disorders and Stroke (NINDS), implemented the SDY Case
Registry in 2015. To meet the ongoing need to produce accurate and
uniform information, CDC and NIH continued the SDY Case Registry in
2018 with 13 awardees through a CDC-based cooperative agreement program
(DP18-1806).
CDC awardees agree to compile a defined set of SDY information
about a defined subset of child deaths through the jurisdiction/state's
existing CDR program. Each of the 13 CDC-funded jurisdiction/state
awardees will, on average, review and enter data on 55 of 720 cases
each year. Additionally, based on historical program information, it is
estimated that approximately half (360) of the 720 estimated SDY cases
each year will be recommended for advanced clinical review by a team of
three medical experts.
OMB approval is requested for three years. The total estimated
annual burden is 511 hours. There are no costs to respondents other
than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
State health personnel........ SDY Module I.... 13 55 10/60 119
[[Page 50125]]
Medical Expert................ Advanced Review. 39 28 15/60 273
State Health Personnel........ SDY Module N.... 13 55 10/60 119
---------------------------------------------------------------
Total hours............... ................ .............. .............. .............. 511
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2021-19163 Filed 9-3-21; 8:45 am]
BILLING CODE 4163-18-P
