Proposed Data Collection Submitted for Public Comment and Recommendations, 25055-25056 [2019-11215]
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Federal Register / Vol. 84, No. 104 / Thursday, May 30, 2019 / Notices
support. Individual members of the
Panel do not attend regularly-scheduled
meetings and do not serve for fixed
terms or a long period of time. Rather,
they are asked to participate in
particular review meetings which
require their type of expertise.
Each SEP meeting will commence in
open session before closing to the public
for the duration of the meeting. The SEP
meeting referenced above will be closed
to the public in accordance with the
provisions set forth in 5 U.S.C. App. 2,
section 10(d), 5 U.S.C. 552b(c)(4), and 5
U.S.C. 552b(c)(6). Grant applications for
AHRQ–HS–19–002, ‘‘Using Data
Analytics to Support Primary Care and
Community Interventions to Improve
Chronic Disease Prevention and
Management and Population Health
(R18),’’ are to be reviewed and
discussed at this meeting. The grant
applications and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the grant applications, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Gopal Khanna,
Director.
[FR Doc. 2019–11241 Filed 5–29–19; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-19–1128; Docket No. CDC–2019–
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 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 information
collection entitled ‘‘State Unintentional
Drug Overdose Reporting System
jbell on DSK3GLQ082PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:08 May 29, 2019
Jkt 247001
(SUDORS).’’ CDC will use the
information collected to perform fatal
unintentional drug overdose
surveillance in a quick and
comprehensive way.
DATES: CDC must receive written
comments on or before July 29, 2019.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0049 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 Jeffery M. Zirger,
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.
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,
PO 00000
Frm 00028
Fmt 4703
Sfmt 4703
25055
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
State Unintentional Drug Overdose
Reporting System (SUDORS) (0920–
1128, Expiration 10/31/2020)—
Revision—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In 2013, there were nearly 44,000
drug overdose deaths, including nearly
36,000 unintentional drug overdose
deaths, in the United States. More
people are now dying of drug overdose
than automobile crashes in the US. 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.
In order 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 that is more
detailed, useful, and timely than 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
inform the selection and targeting of
interventions in all 50 states, the District
of Columbia and Puerto Rico. CDC
requests OMB approval for three years
for this revision to make the following
changes: (1) Expand data collection
from the 50 jurisdictions currently
approved to include 52 jurisdictions
(i.e., all 50 states, Puerto Rico and the
District of Columbia), (2) expand data
E:\FR\FM\30MYN1.SGM
30MYN1
25056
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
]]>Agencies
[Federal Register Volume 84, Number 104 (Thursday, May 30, 2019)]
[Notices]
[Pages 25055-25056]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-11215]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-19-1128; Docket No. CDC-2019-0049]
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 a proposed
information collection entitled ``State Unintentional Drug Overdose
Reporting System (SUDORS).'' CDC will use the information collected to
perform fatal unintentional drug overdose surveillance in a quick and
comprehensive way.
DATES: CDC must receive written comments on or before July 29, 2019.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2019-
0049 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 Jeffery M. Zirger, 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
State Unintentional Drug Overdose Reporting System (SUDORS) (0920-
1128, Expiration 10/31/2020)--Revision--National Center for Injury
Prevention and Control (NCIPC), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In 2013, there were nearly 44,000 drug overdose deaths, including
nearly 36,000 unintentional drug overdose deaths, in the United States.
More people are now dying of drug overdose than automobile crashes in
the US. 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.
In order 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 that is more detailed, useful, and timely than 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 inform the
selection and targeting of interventions in all 50 states, the District
of Columbia and Puerto Rico. CDC requests OMB approval for three years
for this revision to make the following changes: (1) Expand data
collection from the 50 jurisdictions currently approved to include 52
jurisdictions (i.e., all 50 states, Puerto Rico and the District of
Columbia), (2) expand data
[[Page 25056]]
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 6-month time lag,
and (5) 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. This information will help develop,
inform, and assess the progress of drug overdose 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.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Total number
Number of of responses Average burden Total burden
Type of respondent Form name respondents per per response hours (in
respondent (in hours) hours)
----------------------------------------------------------------------------------------------------------------
Public agencies............... Retrieving and 52 1263 30/60 32,838
refile records.
---------------------------------------------------------------
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
