Proposed Data Collection Submitted for Public Comment and Recommendations, 55806-55808 [2022-19565]
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55806
Federal Register / Vol. 87, No. 175 / Monday, September 12, 2022 / Notices
presented to the EXIM Board of
Directors prior to final action on these
Transactions.
DATES: Comments must be received on
or before October 7, 2022 to be assured
of consideration before final
consideration of the transactions by the
Board of Directors of EXIM.
ADDRESSES: Comments may be
submitted through Regulations.gov at
www.regulations.gov. To submit a
comment, enter EIB–2022–0005 under
the heading ‘‘Enter Keyword or ID’’ and
select Search. Follow the instructions
provided at the Submit a Comment
screen. Please include your name,
company name (if any) and EIB–2022–
0005 on any attached document.
SUPPLEMENTARY INFORMATION:
Reference: AP089437XX.
Purpose and Use:
Brief description of the purpose of the
transactions: To support the export of
U.S.-manufactured commercial aircraft
to Switzerland.
Brief non-proprietary description of
the anticipated use of the items being
exported: To be used for air cargo
transport between Switzerland and
other countries.
To the extent that EXIM is reasonably
aware, the item(s) being exported may
be used to produce exports or provide
services in competition with the
exportation of goods or provision of
services by a United States industry.
Parties:
Principal Supplier: The Boeing
Company.
Obligor: Titan Aviation Leasing
Limited—Americas, Inc.
Guarantor(s): Atlas Air Worldwide
Holdings, Inc.
Description of Items Being Exported:
Boeing commercial jet aircraft.
Information on Decision: Information
on the final decision for these
transactions will be available in the
‘‘Summary Minutes of Meetings of
Board of Directors’’ on https://exim.gov/
newsandevents/boardmeetings/board/.
Confidential Information: Please note
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disclosed, would violate the Trade
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States by supplying information that
competitors could use to compete with
companies in the United States.
Authority: Section 3(c)(10) of the
Export-Import Bank Act of 1945, as
amended (12 U.S.C. 635a(c)(10)).
Joyce B. Stone,
Assistant Corporate Secretary.
[FR Doc. 2022–19604 Filed 9–9–22; 8:45 am]
BILLING CODE 6690–01–P
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FEDERAL ELECTION COMMISSION
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Sunshine Act Meeting
TIME AND DATE:
Thursday, September 15,
2022 at 10 a.m.
Hybrid Meeting: 1050 First Street
NE Washington, DC (12th Floor) and
Virtual.
Note: For those attending the meeting
in person, current COVID–19 safety
protocols for visitors, which are based
on the CDC COVID–19 community level
in Washington, DC, will be updated on
the commission’s contact page by the
monday before the meeting. See the
contact page at https://www.fec.gov/
contact/. If you would like to virtually
access the meeting, see the instructions
below.
PLACE:
Centers for Disease Control and
Prevention
[60Day–22–1295; Docket No. CDC–2022–
0105]
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
STATUS: This meeting will be open to the
agencies the opportunity to comment on
public, subject to the above-referenced
a continuing information collection, as
guidance regarding the COVID–19
required by the Paperwork Reduction
community level and corresponding
Act of 1995. This notice invites
health and safety procedures. To access
comment on a proposed information
the meeting virtually, go to the
collection project titled Public Health
commission’s website www.fec.gov and
Accreditation Board (PHAB):
click on the banner to be taken to the
Assessment of Processes and Outcomes.
meeting page.
The purpose of this Extension is to
collect information from health
MATTERS TO BE CONSIDERED:
departments throughout the initial
Draft Advisory Opinion 2022–12:
accreditation and reaccreditation
Ready for Ron.
process to learn about program
Draft Advisory Opinion 2022–17:
processes and the accreditation/
reaccreditation standards, to improve
Warren Democrats.
the program’s quality, and to document
Draft Advisory Opinion 2022–19:
program outcomes and inform decision
Maggie for NH.
making about future program direction.
Final Determination on Eligibility to
DATES: CDC must receive written
Receive Primary Election Public
comments on or before November 14,
Funds—Howie Hawkins and Howie
2022.
Hawkins for Our Future, f/k/a Howie
ADDRESSES
: You may submit comments,
Hawkins 2020 (LRA 1132).
identified by Docket No. CDC–2022–
Management and Administrative
0105 by any of the following methods:
Matters.
• Federal eRulemaking Portal:
CONTACT PERSON FOR MORE INFORMATION: www.regulations.gov. Follow the
Judith Ingram, Press Officer, Telephone: instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
(202) 694–1220.
Collection Review Office, Centers for
Authority: Government in the
Disease Control and Prevention, 1600
Sunshine Act, 5 U.S.C. 552b.
Clifton Road NE, MS H21–8, Atlanta,
Individuals who plan to attend in
Georgia 30329.
Instructions: All submissions received
person and who require special
must include the agency name and
assistance, such as sign language
Docket Number. CDC will post, without
interpretation or other reasonable
change, all relevant comments to
accommodations, should contact Laura
www.regulations.gov.
E. Sinram, Acting Secretary and Clerk,
Please note: Submit all comments
at (202) 694–1040, at least 72 hours
through
the Federal eRulemaking portal
prior to the meeting date.
(www.regulations.gov) or by U.S. mail to
Vicktoria J. Allen,
the address listed above.
Acting Deputy Secretary of the Commission.
FOR FURTHER INFORMATION CONTACT: To
[FR Doc. 2022–19794 Filed 9–8–22; 4:15 pm]
request more information on the
proposed project or to obtain a copy of
BILLING CODE 6715–01–P
the information collection plan and
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SUMMARY:
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55807
Federal Register / Vol. 87, No. 175 / Monday, September 12, 2022 / Notices
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,
electronic, mechanical, or other
the accreditation program began in late
2012 and continue to date. Priorities
focus on gathering feedback for program
improvement and documenting program
outcomes to demonstrate impact and
inform decision making about future
program direction. From 2012–2019, the
Robert Wood Johnson Foundation
(RWJF) and the social science
organization NORC at the University of
Chicago, led evaluation efforts. CDC
assumed support of the evaluation
beginning in 2020 and is seeking OMB
approval to continue data collection.
The purpose of this Information
Collection Request (ICR) is to support
the collection of information from
participating health departments
through a series of five surveys. The
surveys seek to collect longitudinal data
on each health department throughout
their accreditation process. Data
collected through this ICR provides
documentation about the evidence and
value of health department
accreditation.
Respondents will include STLT
health department directors or
designees, one respondent per each
health department. All surveys will be
administered electronically; a link to the
survey website will be provided in an
email invitation. The surveys will be
administered on a quarterly basis and
sent to all health departments that reach
any of five milestones in the
accreditation process (application,
recently accredited, accredited for one
year, approaching reaccreditation, and
reaccreditation). Each health
department will be invited to participate
in each survey once (for a total of five
surveys max per health department).
The total annualized estimated burden
is 100 hours. There are no costs to
respondents other than their time to
participate.
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Public Health Accreditation Board
(PHAB): Assessment of Processes and
Outcomes (OMB Control No. 0920–
1295, Exp. 4/30/2023)—Extension—
Center for State, Tribal, Local and
Territorial Support (CSTLTS), Centers
for Disease Control and Prevention
(CDC)
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) works to protect
America from health, safety, and
security threats, both foreign and
domestic. CDC strives to fulfill this
mission, in part, by supporting state,
tribal, local, and territorial (STLT)
health departments. One mechanism for
supporting STLT health departments is
through CDC’s support of a national,
voluntary accreditation program.
CDC supports the Public Health
Accreditation Board (PHAB), a nonprofit organization that serves as the
independent accrediting body. PHAB,
with considerable input from national,
state, tribal, and local public health
professionals, developed a consensus
set of standards to assess the capacity of
STLT health departments. Between
February 2013 (when the first health
department was accredited) and August
2022, 40 state health departments, 305
local health departments, five Tribal
health departments, and one integrated
system (comprised of 67 local health
departments in one centralized state)
have been accredited. Accreditation is
granted for a five-year period and 68
health departments have successfully
completed the reaccreditation process.
Formal efforts to assess the outcomes of
ESTIMATED ANNUALIZED BURDEN HOURS
lotter on DSK11XQN23PROD with NOTICES1
Type of
respondents
STLT HD
ignee.
STLT HD
ignee.
STLT HD
ignee.
STLT HD
ignee.
STLT HD
ignee.
Number of
respondents
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Directors or Des-
Survey 1: Applicant HDs ............................
60
1
20/60
20
Directors or Des-
Survey 2: Recently Accredited HDs ..........
60
1
20/60
20
Directors or Des-
Survey 3: HDs Accredited One Year .........
60
1
20/60
20
Directors or Des-
Survey 4: HDs Approaching Reaccreditation.
Survey 5: Reaccredited HDs .....................
60
1
20/60
20
60
1
20/60
20
.....................................................................
........................
........................
........................
100
Directors or Des-
Total .................................
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55808
Federal Register / Vol. 87, No. 175 / Monday, September 12, 2022 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–19565 Filed 9–9–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–22–1128]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘State
Unintentional Drug Overdose Reporting
System (SUDORS)’’ to the Office of
Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on April 18,
2022 to obtain comments from the
public and affected agencies. CDC
received one public comment related to
the previous notice. This notice serves
to allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) 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;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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 submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
State Unintentional Drug Overdose
Reporting System (SUDORS) (OMB
Control No. 0920–1128, Exp. 1/31/
2023)—Revision—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
There has been a rapid increase in
opioid overdose deaths since 2013. In
the United States, more people are now
dying of drug overdose than automobile
crashes, although opioids—both opioid
pain relievers (OPRs) and illicit forms
such as heroin—are also a major factor
in overdose-related automobile crashes.
On October 26, 2017, the U.S.
Department of Health and Human
Services (HHS) declared the opioid
overdose epidemic to be a national
public health emergency (PHE).
CDC established the State
Unintentional Drug Overdose Reporting
System (SUDORS) in order to detect
new trends in fatal unintentional drug
overdoses, support targeting of drug
overdose prevention efforts, and assess
the progress of the HHS initiative to
reduce opioid misuse and overdoses.
Respondents are state- or jurisdictionlevel health departments. The SUDORS
surveillance system generates detailed,
timely public health information on
unintentional, fatal opioid-related drug
overdoses and has been used to inform
prevention and response efforts at the
national, state, and local levels.
SUDORS consolidates and supplements
information available to health
departments, including vital statistics
and records created by medical
examiners and coroners (ME/C).
SUDORS is built on a web-based
software platform and a collaborative
surveillance and data integration model
developed by CDC and health
departments to improve understanding
of homicide, suicide, undetermined
deaths, and unintentional firearm
deaths (National Violent Death
Reporting System (NVDRS), OMB
Control No. 0920–0607).
Through SUDORS, CDC currently
collects information that is not provided
on death certificates, such as whether
the drug(s) causing the overdoses were
injected or taken orally; a toxicology
report on the decedent, if available; and
risk factors for fatal drug overdoses
including previous drug overdoses,
decedent’s mental health, and whether
the decedent recently exited a treatment
program. Without this information,
efforts to prevent drug overdose deaths
are often based on limited information
available on the death certificate and
anecdotal evidence.
OMB approval is requested for three
years. Participating states and
jurisdictions will continue to report
SUDORS information to CDC through a
module in the NVDRS web-based
platform. State- and jurisdiction-level
public health departments will be
funded to abstract standardized data
elements from ME/C reports as well as
death certificates. During the next three
years, CDC will remove data collection
activities in Puerto Rico, and update the
burden estimate to reflect the increase
in drug overdose deaths.
CDC requests OMB approval for an
estimated 43,631 annualized burden
hours. There are no costs to respondents
other than their time.
lotter on DSK11XQN23PROD with NOTICES1
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Public Agencies ..............................................
Retrieving and refiling records .......................
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51
12SEN1
Total number
of responses
per
respondent
1,711
Average
burden
per response
(in hours)
30/60
]]>Agencies
[Federal Register Volume 87, Number 175 (Monday, September 12, 2022)]
[Notices]
[Pages 55806-55808]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-19565]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-22-1295; Docket No. CDC-2022-0105]
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 continuing information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed information collection project
titled Public Health Accreditation Board (PHAB): Assessment of
Processes and Outcomes. The purpose of this Extension is to collect
information from health departments throughout the initial
accreditation and reaccreditation process to learn about program
processes and the accreditation/reaccreditation standards, to improve
the program's quality, and to document program outcomes and inform
decision making about future program direction.
DATES: CDC must receive written comments on or before November 14,
2022.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2022-
0105 by any 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 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
[[Page 55807]]
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:
[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
Public Health Accreditation Board (PHAB): Assessment of Processes
and Outcomes (OMB Control No. 0920-1295, Exp. 4/30/2023)--Extension--
Center for State, Tribal, Local and Territorial Support (CSTLTS),
Centers for Disease Control and Prevention (CDC)
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) works to
protect America from health, safety, and security threats, both foreign
and domestic. CDC strives to fulfill this mission, in part, by
supporting state, tribal, local, and territorial (STLT) health
departments. One mechanism for supporting STLT health departments is
through CDC's support of a national, voluntary accreditation program.
CDC supports the Public Health Accreditation Board (PHAB), a non-
profit organization that serves as the independent accrediting body.
PHAB, with considerable input from national, state, tribal, and local
public health professionals, developed a consensus set of standards to
assess the capacity of STLT health departments. Between February 2013
(when the first health department was accredited) and August 2022, 40
state health departments, 305 local health departments, five Tribal
health departments, and one integrated system (comprised of 67 local
health departments in one centralized state) have been accredited.
Accreditation is granted for a five-year period and 68 health
departments have successfully completed the reaccreditation process.
Formal efforts to assess the outcomes of the accreditation program
began in late 2012 and continue to date. Priorities focus on gathering
feedback for program improvement and documenting program outcomes to
demonstrate impact and inform decision making about future program
direction. From 2012-2019, the Robert Wood Johnson Foundation (RWJF)
and the social science organization NORC at the University of Chicago,
led evaluation efforts. CDC assumed support of the evaluation beginning
in 2020 and is seeking OMB approval to continue data collection.
The purpose of this Information Collection Request (ICR) is to
support the collection of information from participating health
departments through a series of five surveys. The surveys seek to
collect longitudinal data on each health department throughout their
accreditation process. Data collected through this ICR provides
documentation about the evidence and value of health department
accreditation.
Respondents will include STLT health department directors or
designees, one respondent per each health department. All surveys will
be administered electronically; a link to the survey website will be
provided in an email invitation. The surveys will be administered on a
quarterly basis and sent to all health departments that reach any of
five milestones in the accreditation process (application, recently
accredited, accredited for one year, approaching reaccreditation, and
reaccreditation). Each health department will be invited to participate
in each survey once (for a total of five surveys max per health
department). The total annualized estimated burden is 100 hours. There
are no costs to respondents other than their time to participate.
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)
--------------------------------------------------------------------------------------------------------------------------------------------------------
STLT HD Directors or Designee......................... Survey 1: Applicant HDs......... 60 1 20/60 20
STLT HD Directors or Designee......................... Survey 2: Recently Accredited 60 1 20/60 20
HDs.
STLT HD Directors or Designee......................... Survey 3: HDs Accredited One 60 1 20/60 20
Year.
STLT HD Directors or Designee......................... Survey 4: HDs Approaching 60 1 20/60 20
Reaccreditation.
STLT HD Directors or Designee......................... Survey 5: Reaccredited HDs...... 60 1 20/60 20
---------------------------------------------------------------
Total............................................. ................................ .............. .............. .............. 100
--------------------------------------------------------------------------------------------------------------------------------------------------------
[[Page 55808]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-19565 Filed 9-9-22; 8:45 am]
BILLING CODE 4163-18-P
