60-day Federal Register Notice

Att B Published 60-Day Federal Register Notice.pdf

State Unintentional Drug Overdose Reporting System (SUDORS)

60-day Federal Register Notice

OMB: 0920-1128

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22890

Federal Register / Vol. 87, No. 74 / Monday, April 18, 2022 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name

Smokeless Tobacco Manufacturers, Packagers, and Importers.

SLT Nicotine Report ...............

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–08214 Filed 4–15–22; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–1128; Docket No. CDC–2022–
0050]

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 continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled State
Unintentional Drug Overdose Reporting
System (SUDORS). This information
collection supports drug overdose
prevention efforts, detects new trends in
fatal unintentional drug overdoses, and
assesses the progress of HHS’s initiative
to reduce opioid abuse.
DATES: CDC must receive written
comments on or before June 17, 2022.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0050 by either of the following methods:
• Federal eRulemaking Portal:
www.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
SUMMARY:

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Number of
respondents

Type of respondents

VerDate Sep<11>2014

17:22 Apr 15, 2022

Jkt 256001

Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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;
Telephone: 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:
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,

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11

Number of
responses per
respondent
1

Average
burden per
response
(in hours)
1,706.5

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
State Unintentional Drug Overdose
Reporting System (SUDORS) (OMB
Control No. 0920–1128, Exp. 10/31/
2023)—Revision—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
This is a Revision request for the
currently approved State Unintentional
Drug Overdose Reporting System
(SUDORS) (OMB Control No. 0920–
1128, Exp. Date 10/31/2023). SUDORS
assists with ongoing surveillance of fatal
unintentional and undetermined intent
drug-related overdoses to support
prevention and response efforts.
In 2013, there were nearly 44,000
drug overdose deaths, including nearly
36,000 unintentional drug overdose
deaths, in the United States, with more
people now dying of drug overdoses
than automobile crashes. A major driver
of the problem are overdoses related to
opioids, both opioid pain relievers
(OPRs) and illicit forms such as heroin.
In order to address this public health
problem, the U.S. Department of Health
and Human Services (HHS) has made
addressing the opioid abuse problem a
high priority.
To support targeting of drug overdose
prevention efforts, detect new trends in
fatal unintentional drug overdoses, and
assess the progress of HHS’s initiative to
reduce opioid abuse and overdoses, the
State Unintentional Drug Overdose
Reporting System (SUDORS) generates
public health surveillance information
at the national, state, and local levels.
This information is more detailed,
useful, and timely than other
information that is currently available.
This collection will detect state and
local community changes in
unintentional and undetermined intent
drug-related overdose mortality faster
and provide in-depth state and local
(e.g., county) information on risk factors
for fatal drug overdose deaths that can

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Federal Register / Vol. 87, No. 74 / Monday, April 18, 2022 / Notices
inform the selection and targeting of
interventions in all 50 states, the District
of Columbia and Puerto Rico. This
information will help develop, inform,
and assess the progress of drug overdose
prevention strategies at both the state
and national levels. Information will
also improve the identification and
response to changes in fatal
unintentional and undetermined intent
drug-related overdose trends at the
local, state, and national level. CDC
obtained OMB approval in 2020 for a
Revision to make the following changes:
(1) Expand data collection from the 50
jurisdictions previously approved to
include 52 jurisdictions (i.e., all 50
states, Puerto Rico and the District of
Columbia), (2) expand data collection
from its current focus on opioid
overdose deaths to a broader focus on
drug overdose deaths, (3) account for

undetermined intent drug overdose
deaths that occurred among all 50 states
in 2017 (64,998 deaths). This Revision
request will use the total number of
unintentional or undetermined intent
drug overdose deaths in the US from
2020 (87,302 deaths). The total number
of unintentional or undetermined intent
drug overdose deaths per jurisdiction
was estimated by dividing the total
number of drug overdose deaths, 87,302
by the number of participating health
departments, 51, or approximately 1,711
deaths per participating health
department. This created an increase
from the previously approved burden.
CDC requests OMB approval for an
estimated 43,631 annual burden hours.
There are no costs to respondents other
than their time to participate.

increasing data collection burden
related to large increases in drug
overdose deaths, and (4) update the
web-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.
CDC requests a three-year approval for
an additional Revision request to
continue collecting SUDORS data. The
current Revision request has the
following change: The burden estimate
has been updated to reflect the increase
in the number of drug overdose deaths.
This new burden estimate is higher than
the previously approved estimate of
32,838 hours because the previous
burden estimates were based on the
number of unintentional and

ESTIMATED ANNUALIZED BURDEN HOURS
Total
number of
responses per
respondent

Average
burden per
response
(in hours)

Total
burden
hours
(in hours)

Form name

Public Agencies ................................

Retrieving and refiling records .........

51

1,711

30/60

43,631

Total ...........................................

...........................................................

........................

........................

........................

43,631

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–08217 Filed 4–15–22; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–0881; Docket No. CDC–2022–
0049]

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.

SUMMARY:
khammond on DSKJM1Z7X2PROD with NOTICES

Number of
respondents

Type of respondent

VerDate Sep<11>2014

17:22 Apr 15, 2022

Jkt 256001

This notice invites comment on a
proposed information collection project
titled Laboratory Response Network
(LRN) Data Calls. This project will help
CDC conduct special data calls to obtain
additional information from LRN
laboratories regarding biological or
chemical terrorism, or emerging
infectious disease preparedness.
DATES: CDC must receive written
comments on or before June 17, 2022.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0049 by either 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

PO 00000

Frm 00024

Fmt 4703

Sfmt 4703

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;
Telephone: 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:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including

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18APN1


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File Modified2022-04-16
File Created2022-04-16

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