Proposed Data Collection Submitted for Public Comment and Recommendations, 52575-52577 [2022-18443]
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52575
Federal Register / Vol. 87, No. 165 / Friday, August 26, 2022 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Form number & name
57.308 Hemovigilance Adverse Reaction—Allergic Transfusion Reaction .....
57.309 Hemovigilance Adverse Reaction—Delayed Hemolytic Transfusion
Reaction .......................................................................................................
57.310 Hemovigilance Adverse Reaction—Delayed Serologic Transfusion
Reaction .......................................................................................................
57.311 Hemovigilance Adverse Reaction—Febrile Non-hemolytic Transfusion Reaction ............................................................................................
57.312 Hemovigilance Adverse Reaction—Hypotensive Transfusion Reaction ................................................................................................................
57.313 Hemovigilance Adverse Reaction—Infection ......................................
57.314 Hemovigilance Adverse Reaction—Post Transfusion Purpura ...........
57.315 Hemovigilance Adverse Reaction—Transfusion Associated Dyspnea
57.316 Hemovigilance Adverse Reaction—Transfusion Associated Graft vs.
Host Disease ................................................................................................
57.317 Hemovigilance Adverse Reaction—Transfusion Related Acute Lung
Injury .............................................................................................................
57.318 Hemovigilance Adverse Reaction—Transfusion Associated Circulatory Overload .........................................................................................
57.319 Hemovigilance Adverse Reaction—Unknown Transfusion Reaction ..
57.320 Hemovigilance Adverse Reaction—Other Transfusion Reaction ........
57.400 Outpatient Procedure Component—Annual Facility Survey ...............
57.401 Outpatient Procedure Component—Monthly Reporting Plan .............
57.402 Outpatient Procedure Component Same Day Outcome Measures ....
57.403 Outpatient Procedure Component—Monthly Denominators for Same
Day Outcome Measures ..............................................................................
57.404 Outpatient Procedure Component—SSI Denominator ........................
57.405 Outpatient Procedure Component—Surgical Site (SSI) Event ...........
57.500 Outpatient Dialysis Center Practices Survey ......................................
57.501 Dialysis Monthly Reporting Plan ..........................................................
57.502 Dialysis Event ......................................................................................
57.503 Denominator for Outpatient Dialysis ....................................................
57.504 Prevention Process Measures Monthly Monitoring for Dialysis ..........
57.505 Dialysis Patient Influenza Vaccination .................................................
57.506 Dialysis Patient Influenza Vaccination Denominator ...........................
57.507 Home Dialysis Center Practices Survey .............................................
Weekly Healthcare Personnel Influenza Vaccination Cumulative Summary
for Non-Long-Term Care Facilities ...............................................................
Weekly Healthcare Personnel Influenza Vaccination Cumulative Summary
for Long-Term Care Facilities ......................................................................
Weekly Resident Influenza Vaccination Cumulative Summary for Long-Term
Care Facilities ..............................................................................................
Annual Healthcare Personnel Influenza Vaccination Summary ......................
Total ..........................................................................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–18442 Filed 8–25–22; 8:45 am]
BILLING CODE 4163–18–P
20/60
667
500
1
20/60
167
500
2
20/60
333
500
4
20/60
667
500
500
500
500
1
1
1
1
20/60
20/60
20/60
20/60
167
167
167
167
500
1
20/60
167
500
1
20/60
167
500
500
500
700
700
200
2
1
1
1
12
1
20/60
20/60
20/60
10/60
15/60
40/60
333
167
167
117
2,100
133
200
700
700
7,400
7,400
7,400
7,400
1,730
615
615
450
400
100
5
1
12
30
24
12
50
5
1
40/60
40/60
40/60
125/60
5/60
27/60
10/60
75/60
10/60
10/60
36/60
53,333
46,667
2,333
15,417
7,400
99,900
29,600
25,950
5,125
3075
270
125
52
60/60
6,500
1,200
52
60/60
62,400
2,500
5,000
52
1
60/60
120/60
130,000
10,000
........................
........................
........................
1,614,345
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–1166; Docket No. CDC–2022–
0100]
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
lotter on DSK11XQN23PROD with NOTICES1
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
SUMMARY:
Jkt 256001
PO 00000
Frm 00076
Fmt 4703
Total burden
(in hours)
4
AGENCY:
16:59 Aug 25, 2022
Avg. burden
per response
(in hours)
500
Proposed Data Collection Submitted
for Public Comment and
Recommendations
VerDate Sep<11>2014
Number of
responses per
respondent
Sfmt 4703
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 Poison Center
Collaborations for Public Health
Emergencies. This proposed collection
will allow CDC to quickly characterize
potential exposures identified through
the National Poison Data System
(NPDS), help determine potential risk
factors, identify illnesses related to the
public health emergency, and improve
the public health response to the
incident.
E:\FR\FM\26AUN1.SGM
26AUN1
52576
Federal Register / Vol. 87, No. 165 / Friday, August 26, 2022 / Notices
CDC must receive written
comments on or before October 25,
2022.
DATES:
You may submit comments,
identified by Docket No. CDC–2022–
0100 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
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;
lotter on DSK11XQN23PROD with NOTICES1
ADDRESSES:
VerDate Sep<11>2014
16:59 Aug 25, 2022
Jkt 256001
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
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 TM, formerly known as the
American Association of Poison Control
Centers (AAPCC). America’s Poison
Centers TM is a national network of 55
poison centers working to prevent and
treat poison exposures. America’s
Poison Centers TM 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 TM 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
event 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 event has resulted in calls
to a poison center, and the poison center
agrees to conduct the call-back data
PO 00000
Frm 00077
Fmt 4703
Sfmt 4703
collection; (5) the event 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
E:\FR\FM\26AUN1.SGM
26AUN1
52577
Federal Register / Vol. 87, No. 165 / Friday, August 26, 2022 / Notices
respondents from 150 to 500 per callback investigation.
Based on these revisions, the total
number of annual respondents
requested is 1,500, which is an increase
of 1,200 over the 300 respondents
previously approved. 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
Average
burden per
response
(in hours)
Total burden
(in hours)
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 ...
1,200
150
150
1
1
1
10/60
10/60
10/60
200
25
25
Total ...........................................
...........................................................
........................
........................
........................
250
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–18443 Filed 8–25–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–22–1291; Docket No. CDC–2022–
0097]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
ACTION:
Notice with comment period.
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 Generic
Information Collection Request for
Cognitive Testing and Pilot Testing for
the National Center for Chronic Disease
Prevention and Health Promotion. The
Generic Clearance is needed to support
methodological studies that improve
information quality and the efficiency of
information collection.
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Number of
responses per
respondent
Number of
respondents
Type of respondents
CDC must receive written
comments on or before October 25,
2022.
DATES:
VerDate Sep<11>2014
16:59 Aug 25, 2022
Jkt 256001
You may submit comments,
identified by Docket No. CDC–2022–
0097 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
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: 404–639–7118; 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
ADDRESSES:
PO 00000
Frm 00078
Fmt 4703
Sfmt 4703
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
Generic Information Collection
Request (ICR) for Cognitive Testing and
Pilot Testing for the National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP) (OMB Control
No. 0921–1291, Exp. 03/31/2023)—
Extension—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC’s National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP) plans has
established a Generic Clearance (OMB
Control No. 0920–1291) to support
information collection for cognitive
testing and pilot testing activities.
Information collections that support the
E:\FR\FM\26AUN1.SGM
26AUN1
]]>Agencies
[Federal Register Volume 87, Number 165 (Friday, August 26, 2022)]
[Notices]
[Pages 52575-52577]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-18443]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-22-1166; Docket No. CDC-2022-0100]
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 Poison Center Collaborations for Public Health Emergencies. This
proposed collection will allow CDC to quickly characterize potential
exposures identified through the National Poison Data System (NPDS),
help determine potential risk factors, identify illnesses related to
the public health emergency, and improve the public health response to
the incident.
[[Page 52576]]
DATES: CDC must receive written comments on or before October 25, 2022.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2022-
0100 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 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: [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
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 \TM\, formerly known
as the American Association of Poison Control Centers (AAPCC).
America's Poison Centers \TM\ is a national network of 55 poison
centers working to prevent and treat poison exposures. America's Poison
Centers \TM\ 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 \TM\ 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 event 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 event has resulted in calls to a poison center, and the
poison center agrees to conduct the call-back data collection; (5) the
event 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
[[Page 52577]]
respondents from 150 to 500 per call-back investigation.
Based on these revisions, the total number of annual respondents
requested is 1,500, which is an increase of 1,200 over the 300
respondents previously approved. 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 respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Adult Poison Center Callers... Call-back 1,200 1 10/60 200
Questionnaire
for Self.
Adolescent Poison Center Call-back 150 1 10/60 25
Callers. Questionnaire
for Self.
Parent or Guardian Poison Call-back 150 1 10/60 25
Center Callers. Questionnaire
for Proxy.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 250
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-18443 Filed 8-25-22; 8:45 am]
BILLING CODE 4163-18-P
