Agency Forms Undergoing Paperwork Reduction Act Review, 74149-74151 [2022-26306]
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Federal Register / Vol. 87, No. 231 / Friday, December 2, 2022 / Notices
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SUPPLEMENTARY INFORMATION:
A. Purpose
The Mission-Support Customer
Satisfaction Survey (CSS) is an annual
survey led by the Office of Management
and Budget (OMB) and managed by the
General Services Administration (GSA).
The CSS began in 2015 as part of the
Obama Administration’s President’s
Management Agenda (PMA).
The CSS asks Federal employees to
rate how satisfied they are with missionsupport functions and services, how
important specific mission-support
services are to achieving mission
outcomes, and whether a function
serves as an effective strategic partner.
Employees are asked to rate their
perception of satisfaction, importance,
and strategic partnership for 24 service
areas on a seven-point Likert Scale
within the following four support
functions (functions are in bold):
Contracting: Pre-Award Activities;
Contract Administration; Purchase Card
Management.
Finance: Budget Formulation; Budget
Execution; Financial Management
Information & Analysis; Bill Payments;
Bill Collections; Financial Risk
Management.
Human Capital: Recruiting & Hiring;
Training & Development; Work/Life
Support; Employee Relations; Labor
Relations; Performance & Recognition
Management; Workforce Planning &
Succession; Time & Attendance
Management; Benefits Management;
Retirement Planning & Processing.
Information Technology: IT Support;
IT Communications & Collaboration; IT
Equipment; Operations & Maintenance
(O&M); Development, Modernization &
Enhancement (DM&E).
The CSS is an annual, non-mandatory
survey typically sent in early spring to
all federal civilian employees at the 24
CFO Act Agencies.
The survey is distributed through
email and responses are collected
through an online survey platform. Each
email sent contains a unique link to take
the survey. Email contacts are obtained
through the Office of Personnel
Management’s (OPM) Enterprise Human
Resources Integration-Statistical Data
Mart (EHRI–SDM). The EHRI–SDM is an
information system that supports
statistical analyses of federal personnel
management programs. Agencies submit
data from their personnel systems to the
EHRI–SDM.
Agencies may choose to supplement
or edit the EHRI–SDM email list for the
purposes of this survey.
Survey reminders are sent once per
week to those who have not yet taken
the survey starting 7 days after the
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initial launch date until the closing of
the survey. The survey is typically open
for 6 to 8 weeks.
Individual survey responses are
tracked for completeness so that
reminders are sent only to those who
have not yet taken the survey.
This is a confidential survey. To
prevent identification of individual
respondents, average satisfaction scores
are excluded where the number of
responses is fewer than 10. Once the
survey is closed, all personal
identifiable information (PII) is stripped
from the data to protect privacy.
Survey participants only answered
questions related to functions or
services they had interaction within the
previous year.
The response rate from year to year is
approximately 20%.
Survey participants are allowed to opt
out or choose not to take the survey.
The CSS is 508 compliant.
The CSS data is used by the Federal
Government for three primary reasons:
• To provide a significant measure for
quality of service provided, so that
agencies can evaluate functional
performance on quality as well as cost.
• To allow agencies to compare their
performance to other agencies at the
agency and bureau level.
• To provide the center of
government a valuable data set to
analyze and provide actionable insights
for mission-support performance
improvement.
Here are other specifics around how
we plan to share the data:
• The items and the results of the
items will be made publicly available
for Federal agencies to assess their
scores to identify areas for
improvement;
• The general public, including
researchers and the media, will also
have access to this information;
• The collections are voluntary;
• Access to completed surveys will be
limited to GSA and contractors who are
involved in collecting and/or preparing
the information for further analysis at
OMB and distribution to other agencies:
• Information is only shared for the
for the whole population and for certain
subgroups. Neither federal agencies nor
the public will receive data by
subgroups that could be used to identify
a specific individual or a person’s
specific response to a survey question.
The Agency has established a
manager/managing entity to serve for
this generic clearance and will conduct
an independent review of each
information collection to ensure
compliance with the terms of this
clearance prior to submitting each
collection to OMB.
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74149
B. Annual Reporting Burden
Respondents: 300,100.
Responses per Respondent: 1.
Total Annual Responses: 1.
Hours per Response: 0.093 (338
seconds).
Total Burden Hours: 28,176.06.
C. Public Comments
A 60-day notice published in the
Federal Register at 87 FR 39095 on June
30, 2022. No comments were received.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the Regulatory Secretariat Division by
calling 202–501–4755 or emailing
GSARegSec@gsa.gov. Please cite OMB
Control No. ‘‘3090–XXXX Generic
Clearance for the Collection of the
Mission-Support Customer Satisfaction
Survey’’ in all correspondence.
Beth Anne Killoran,
Deputy Chief Information Officer.
[FR Doc. 2022–26286 Filed 12–1–22; 8:45 am]
BILLING CODE 6820–14–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–23–1166]
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 ‘‘Poison Center
Collaborations for Public Health
Emergencies (PCCPHE)’’ 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 August
26, 2022 to obtain comments from the
public and affected agencies. CDC
received no substantive public
comments 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;
E:\FR\FM\02DEN1.SGM
02DEN1
74150
Federal Register / Vol. 87, No. 231 / Friday, December 2, 2022 / Notices
(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
Poison Center Collaborations for
Public Health Emergencies
(PCCPHE)(OMB Control No. 0920–1166,
Exp. 04/30/2023)—Revision—National
Center for Environmental Health
(NCEH), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) is requesting a threeyear Paperwork Reduction Act (PRA)
Revision of the Generic Information
Collection Request (Generic ICR) titled
Poison Center Collaborations for Public
Health Emergencies (PCCPHE) (OMB
Control No. 0920–1166; Expiration Date
04/30/2023).
CDC’s key partner is America’s Poison
Centers, formerly known as the
American Association of Poison Control
Centers (AAPCC). America’s Poison
Centers is a national network of 55
poison centers working to prevent and
treat poison exposures. America’s
Poison Centers manages its existing
surveillance system called the National
Poison Data System (NPDS) and
provides CDC access to monitor this
system under a cooperative agreement
and a data license agreement.
When a public health emergency of
interest emerges in NPDS, the CDC and
America’s Poison Centers hold a
meeting to mutually decide whether the
incident needs further investigation. For
a public health emergency to be selected
for call-back, adverse health effects must
have occurred, and a response is needed
to prevent further morbidity and
mortality. The event must meet the
following criteria: (1) the event is a
public health emergency causing
adverse health effects; (2) timely data
are urgently needed to inform rapid
public health action to prevent or
reduce injury, disease, or death; (3) the
incident is characterized by a natural or
man-made disaster, contaminated food
or water, a new or existing consumer
product, or an emerging public health
threat; (4) the incident has resulted in
calls to a poison center, and the poison
center agrees to conduct the call-back
data collection; (5) the incident is
domestic; and (6) data collection will be
completed in 60 days or less.
The purpose of this Generic ICR is to
create a timely mechanism to allow
poison centers, supported by CDC, to
follow-up with callers during select
public health emergencies on exposure
and health. These PCCPHE Generic
Information Collections (GenICs) will
obtain information on sources of
exposure, scenario of exposure, health
seeking behaviors following exposure,
and awareness of health communication
messaging. These additional data can
help CDC identify interventions to
improve health messaging meant to
reduce exposure; improve disaster and
emergency response; and prevent future
events for the specific area or incident
of interest.
Trained poison center staff will
conduct the call-back telephone survey
or will facilitate the call-back web
survey, after administering consent.
Respondents will include individuals
who call poison centers about exposures
related to the select public health
emergencies. These respondents include
adults, 18 years and older; adolescents,
15 to less than 18 years; and parents or
guardians on behalf of their children
less than 15 years of age.
In 2019, a PCCPHE GenIC, titled ‘‘Risk
Factors for Harmful Algal Blooms
(HABs),’’ was conducted to identify
sources of and risk factors for HAB
exposures. New information gained
about HAB exposures were used
improve HAB incident response,
communication, and outreach at the
state and national level. During the past
three-year approval period, no PCCPHE
GenICs were conducted; however, two
NPDS-related follow-up studies were
implemented using the Secretary’s
Public Health Emergency PRA Waiver
for COVID–19. During a non-pandemic
situation, these two studies would have
used this Generic ICR. These studies
assessed unintentional exposures
associated with cleaning products (e.g.,
bleach, hand sanitizers) in home
settings to determine knowledge,
attitudes, and practices regarding
cleaning behaviors and help guide
public health messaging.
Based on CDC’s past experience, the
following revisions affecting public
burden are proposed. CDC plans to
increase the annual number of public
health emergencies of interest from two
to three per year. CDC will reduce the
estimated time per response from 40
minutes to 10 minutes. CDC plans to
add web surveys as a second secure
mode of collection to the currently
approved telephone surveys. CDC will
also increase the annual number of
respondents from 150 to 500 per callback investigation.
Based on these revisions, the annual
time burden requested is 250 hours,
which is an increase of 50 hours over
the 200 hours previously approved.
There is no cost to the respondents
other than their time.
lotter on DSK11XQN23PROD with NOTICES1
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Adult Poison Center Callers ...........................
Adolescent Poison Center Callers ..................
Parent or Guardian Poison Center Callers .....
Call-back Questionnaire for Self ....................
Call-back Questionnaire for Self ....................
Call-back Questionnaire for Proxy .................
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1,200
150
150
02DEN1
Number of
responses per
respondent
1
1
1
Average burden per
response
(in hours)
10/60
10/60
10/60
74151
Federal Register / Vol. 87, No. 231 / Friday, December 2, 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. 2022–26306 Filed 12–1–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–23–22CB]
Agency Forms Undergoing Paperwork
Reduction Act Review
lotter on DSK11XQN23PROD with NOTICES1
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Assessment for
the Get Ahead of Sepsis (GAOS)
Consumer and Healthcare Professional
Campaign’’ 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 January
31, 2022, to obtain comments from the
public and affected agencies. CDC
received two comments 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
Assessment for the Get Ahead of
Sepsis (GAOS) Consumer and
Healthcare Professional Campaign—
New—National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Sepsis is a life threating emergency,
and it is the body’s overactive and toxic
response to an infection. Each year 1.7
million adults in the United States
develop sepsis, with 270,000 fatalities.
Sepsis is the leading cause of death in
hospitals and one out of three hospital
fatalities are due to sepsis infection.
Sepsis management in U.S. hospitals is
the highest when compared to inpatient
cost for all other medical conditions.
Annual costs are estimated to be over
$62 billion.
In media and public health
campaigns, antimicrobial resistance and
sepsis are rarely presented together
which does not make their linkage
apparent. It has been concluded that
sepsis and antimicrobial stewardship
should not be discussed in isolation.
Surprisingly, 24% of adults in the U.S.
have never heard of sepsis, so this
presents a unique opportunity for future
messaging campaigns.
The goals of the Get Ahead of Sepsis
(GAOS) educational campaign are to
prevent and reduce infections that lead
to sepsis and to optimize healthcare
quality and patient safety by raising
awareness, knowledge, and motivating
behavior change related to sepsis
prevention, early recognition, and
appropriate treatment among consumer
and healthcare professional (HCP)
audiences. A panel survey will be
utilized to recruit participants. Surveys
will be distributed to consumer
audiences and HCPs both before and
after the media campaign and partner
outreach.
Consumer audiences include:
(1) Cancer patients and their
caregivers,
(2) Patients who survived severe
COVID–19 or sepsis and their
caregivers,
(3) Parents of children 12 and
younger,
(4) Adults who care for a family
member age 65+, (5) Men aged 65+ with
one or more chronic conditions, and (6)
Healthy adults 65+
HCP audiences include:
(1) Emergency Medical Services
personnel,
(2) Nurse Practitioners and Physician
Assistants who work at urgent care
clinics,
(3) Emergency Department triage
nurses,
(4) General medical ward staff,
(5) Primary care physicians,
(6) Long-term care (LTC) nurses, and
(7) LTC medical technicians and
sitters.
This program evaluation will assist
CDC in determining if the GAOS media
campaign, along with partner outreach,
was successful in raising knowledge and
awareness and motivating behavior
change among consumer and HCP
audiences in select markets. The
information gathered from this
evaluation will also be used to inform
refinement and implementation of the
campaign (materials and tactics).
CDC requests OMB approval for an
estimated 1366 annual burden hours.
There is no cost to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Consumers ......................................................
GAOS Consumer ...........................................
Pre-Campaign web survey .............................
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945
02DEN1
Number of
responses per
respondent
1
Average burden
per response
(in hours)
20/60
]]>Agencies
[Federal Register Volume 87, Number 231 (Friday, December 2, 2022)]
[Notices]
[Pages 74149-74151]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-26306]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-23-1166]
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 ``Poison Center Collaborations for Public
Health Emergencies (PCCPHE)'' 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 August 26, 2022 to obtain comments from the public and
affected agencies. CDC received no substantive public comments 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;
[[Page 74150]]
(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
Poison Center Collaborations for Public Health Emergencies
(PCCPHE)(OMB Control No. 0920-1166, Exp. 04/30/2023)--Revision--
National Center for Environmental Health (NCEH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) is requesting
a three-year Paperwork Reduction Act (PRA) Revision of the Generic
Information Collection Request (Generic ICR) titled Poison Center
Collaborations for Public Health Emergencies (PCCPHE) (OMB Control No.
0920-1166; Expiration Date 04/30/2023).
CDC's key partner is America's Poison Centers, formerly known as
the American Association of Poison Control Centers (AAPCC). America's
Poison Centers is a national network of 55 poison centers working to
prevent and treat poison exposures. America's Poison Centers manages
its existing surveillance system called the National Poison Data System
(NPDS) and provides CDC access to monitor this system under a
cooperative agreement and a data license agreement.
When a public health emergency of interest emerges in NPDS, the CDC
and America's Poison Centers hold a meeting to mutually decide whether
the incident needs further investigation. For a public health emergency
to be selected for call-back, adverse health effects must have
occurred, and a response is needed to prevent further morbidity and
mortality. The event must meet the following criteria: (1) the event is
a public health emergency causing adverse health effects; (2) timely
data are urgently needed to inform rapid public health action to
prevent or reduce injury, disease, or death; (3) the incident is
characterized by a natural or man-made disaster, contaminated food or
water, a new or existing consumer product, or an emerging public health
threat; (4) the incident has resulted in calls to a poison center, and
the poison center agrees to conduct the call-back data collection; (5)
the incident is domestic; and (6) data collection will be completed in
60 days or less.
The purpose of this Generic ICR is to create a timely mechanism to
allow poison centers, supported by CDC, to follow-up with callers
during select public health emergencies on exposure and health. These
PCCPHE Generic Information Collections (GenICs) will obtain information
on sources of exposure, scenario of exposure, health seeking behaviors
following exposure, and awareness of health communication messaging.
These additional data can help CDC identify interventions to improve
health messaging meant to reduce exposure; improve disaster and
emergency response; and prevent future events for the specific area or
incident of interest.
Trained poison center staff will conduct the call-back telephone
survey or will facilitate the call-back web survey, after administering
consent. Respondents will include individuals who call poison centers
about exposures related to the select public health emergencies. These
respondents include adults, 18 years and older; adolescents, 15 to less
than 18 years; and parents or guardians on behalf of their children
less than 15 years of age.
In 2019, a PCCPHE GenIC, titled ``Risk Factors for Harmful Algal
Blooms (HABs),'' was conducted to identify sources of and risk factors
for HAB exposures. New information gained about HAB exposures were used
improve HAB incident response, communication, and outreach at the state
and national level. During the past three-year approval period, no
PCCPHE GenICs were conducted; however, two NPDS-related follow-up
studies were implemented using the Secretary's Public Health Emergency
PRA Waiver for COVID-19. During a non-pandemic situation, these two
studies would have used this Generic ICR. These studies assessed
unintentional exposures associated with cleaning products (e.g.,
bleach, hand sanitizers) in home settings to determine knowledge,
attitudes, and practices regarding cleaning behaviors and help guide
public health messaging.
Based on CDC's past experience, the following revisions affecting
public burden are proposed. CDC plans to increase the annual number of
public health emergencies of interest from two to three per year. CDC
will reduce the estimated time per response from 40 minutes to 10
minutes. CDC plans to add web surveys as a second secure mode of
collection to the currently approved telephone surveys. CDC will also
increase the annual number of respondents from 150 to 500 per call-back
investigation.
Based on these revisions, the annual time burden requested is 250
hours, which is an increase of 50 hours over the 200 hours previously
approved. There is no cost to the respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Adult Poison Center Callers........... Call-back Questionnaire 1,200 1 10/60
for Self.
Adolescent Poison Center Callers...... Call-back Questionnaire 150 1 10/60
for Self.
Parent or Guardian Poison Center Call-back Questionnaire 150 1 10/60
Callers. for Proxy.
----------------------------------------------------------------------------------------------------------------
[[Page 74151]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-26306 Filed 12-1-22; 8:45 am]
BILLING CODE 4163-18-P
