Proposed Data Collection Submitted for Public Comment and Recommendations, 3542-3544 [2022-01260]
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3542
Federal Register / Vol. 87, No. 15 / Monday, January 24, 2022 / Notices
Prevention, 100 Totius Street,
Groenkloof, Pretoria, South Africa,
Telephone: 800–232–6348, Email:
edu9@cdc.gov.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
The
single-source award will support the
SAG in four broad areas of public health
surveillance and response:
Communicable (e.g., HIV and TB) and
non-communicable disease surveillance,
public health laboratory capacity, public
health workforce development, and
global health security. The NICD, under
the National Public Health Institute of
South Africa (NAPHISA), is in a unique
position to conduct this work, through
an act of parliament mandating the
organization to provide microbiology,
virology, epidemiology, surveillance
and public health research and training
to support the government’s response to
communicable disease threats.
SUPPLEMENTARY INFORMATION:
Summary of the Award
Recipient: National Institute for
Communicable Diseases (NICD), South
Africa.
Purpose of the Award: The purpose of
this award is to provide accurate,
timely, and high-quality strategic
information to enable the SAG to track
critical infectious disease pathogens,
monitor interventions, and inform
policy and programming to reduce
disease transmission and burden.
Amount of Award: The approximate
year 1 funding amount will be
$5,000,000 in Federal Fiscal Year (FFY)
2022 funds, subject to the availability of
funds. Annual award amounts for years
2–5 will be set at continuation.
Authority: This program is authorized
under Public Law 108–25 (the United
States Leadership Against HIV AIDS,
Tuberculosis and Malaria Act of 2003).
Period of Performance: September 30,
2022, through September 29, 2027.
Dated: January 19, 2022.
Terrance Perry,
Chief Grants Management Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2022–01271 Filed 1–21–22; 8:45 am]
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Centers for Disease Control and
Prevention
[60Day–22–22BY; Docket No. CDC–2022–
0008]
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 Importation Regulations (42 CFR
71 subpart F), which specifies the
requirements for importing animals or
animal products that are regulated by
CDC into the United States.
DATES: CDC must receive written
comments on or before March 25, 2022.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0008 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 H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
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; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
SUMMARY:
PO 00000
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Fmt 4703
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(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
Importation Regulations (42 CFR 71
Subpart F)—New—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
This is a request for a new
information collection to consolidate
forms and information collections
related to the importation of animals,
animal products, and human remains
into one information collection. This
information collection was previously
part of three separate, OMB-approved
information collections: (1) 0920–1034
(expires 3/31/2022), (2) 0920–0263
(expires 9/30/2023), and (3) 0920–0199
(expires 8/31/2024). CDC is requesting a
three-year OMB clearance for this new,
combined information collection.
Section 361 of the Public Health
Service Act (PHSA) (42 U.S.C. 264)
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3543
Federal Register / Vol. 87, No. 15 / Monday, January 24, 2022 / Notices
authorizes the Secretary of Health and
Human Services to make and enforce
regulations necessary to prevent the
introduction, transmission or spread of
communicable diseases from foreign
countries into the United States. The
Statute, and the existing regulations
governing foreign quarantine activities
(42 CFR 71), authorize quarantine
officers and other personnel to inspect
and undertake necessary control
measures with respect to conveyances,
persons, and shipments of animals and
etiologic agents in order to protect the
public’s health.
CDC regulations govern the
importation of animals and animal
products capable of causing human
disease. Animals that are regulated by
CDC are dogs, cats, turtles, snakes,
lizards, non-human primates (NHP),
civets, African rodents, and bats. CDC
controls the importation of these
animals to ensure that these animals, or
animal products, being imported into
the United States meet CDC regulations.
CDC does this through a permitting
process for certain animals.
On June 16, 2021 CDC published a
Federal Register Notice informing the
public about a temporary suspension of
dogs entering the United States from
high-risk rabies countries. The canine
rabies virus variant (CRVV) was
declared eliminated in the United States
in 2007. The importation of just one dog
infected with CRVV risks reintroduction of the virus into the United
States resulting in a potential public
be imported for bona fide scientific,
educational, or exhibition purposes, as
defined in the regulations. Forms for the
importation of NHPs are currently under
information collection 0920–0263.
These forms will move into this new
information collection to consolidate all
forms related to the importation of
animals or animal products into one
collection.
A new form to request a permit to
import a regulated animal that is neither
a dog nor an NHP (e.g., turtles, African
rodents, civets) is included in this
information collection. It also
incorporates the addition of bats, which
is currently approved under OMB
control number 0920–0199.
Regarding human remains, the
Division of Global Migration and
Quarantine (DGMQ) works with the
Division of Select Agents and Toxins
(DSAT) on the importation for human
remains. DGMQ requests death
certificates from those wishing to import
remains and then determines if the
importer will need a permit, which is
issued by DSAT and will remain in
0920–0199.
Lastly, people importing animal
products must make a statement or
provide documentation demonstrating
that the animal product is not
infectious.
CDC requests approval for an
estimated 60,215 annual burden hours.
There are no costs to respondents other
than their time to participate.
health risk with consequent monetary
cost and potential loss of human and
animal life. Since 2015 there have been
four known rabid dogs imported into
the United States.
During the suspension period, CDC
will issue permits for importers with
dogs who have been in a high-risk
CRVV country within the last six
months and do not have a current, valid
U.S.-issued rabies vaccination
certificate. Only importers who are
permanently relocating to the United
States, are a US government employee
traveling on official orders, are an owner
of a service dog that is trained to assist
them with a disability, are an individual
importing dogs for science, education,
exhibition, or law enforcement
purposes, or people who traveled with
their dog before July 31, 2021 are
eligible to apply for a permit. Dogs from
CRVV-free or low risk countries and
dogs with valid U.S.-issued rabies
vaccination certificates that are
microchipped, healthy, and at least six
months of age do not require a permit.
The current permit application to
import a dog is under collection 0920–
1034. When a dog or cat arrives at an
airport and is sick or dead, importers are
required to notify CDC. There is no form
for this notification.
Other animals that require a permit,
and are included in this information
collection are NHPs, which can carry of
number of diseases that can cause
severe infections in people. NHPs may
not be imported as pets and may only
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)
Total burden
hours
Form name
Dog Importers (42 CFR 71.51(c)(2),
(d)).
NHP Importers (42 CFR 71.53) ........
Dog Permit Application Form ...........
60,000
1
60/60
60,000
120
1
15/60
30
CFR
NHP Shipment Arrival Notification
Form.
NHP Importer Form ..........................
15
1
120/60
30
CFR
Other animal import form .................
2
1
30/60
1
CFR
Record of sickness or death ............
43
1
60/60
43
CFR
Provide death certificate ..................
50
1
15/60
13
CFR
Statement or documentation of noninfectiousness.
391
1
15/60
98
Total ...........................................
...........................................................
........................
........................
........................
60,215
First Time NHP Importer (42
71.53).
Regulated Animal Importer (42
71).
Dog and Cat Importers (42
71.51(b)(3)).
Human Remains Importers (42
71.55, 42 CFR 71.32).
Importer of animal products (42
71.32).
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Number of
responses per
respondent
Number of
respondents
Type of respondents
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3544
Federal Register / Vol. 87, No. 15 / Monday, January 24, 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. 2022–01260 Filed 1–21–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Notice of Award of a Single-Source
Cooperative Agreement To Fund the
Republican AIDS Center, Kyrgyz
Republic
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), located
within the Department of Health and
Human Services (HHS), announces the
award of approximately $2,000,000 for
Year 1 of funding to the Republican
AIDS Center, Kyrgyz Republic (KR). The
award will build on previous
President’s Emergency Plan for AIDS
Relief (PEPFAR) program support to
ensure continuity of high-quality HIV
services to existing clients across the
HIV cascade, the steps of care (from
diagnosis to achieving viral load (VL)
suppression) for people living with HIV
(PLHIV), and achieve the Joint United
Nations Programme on HIV/AIDs
(UNAIDS) 95–95–95 goals (95% of HIVpositive individuals knowing their
status, 95% of those receiving ART
[Antiretroviral therapy], and 95% of
those achieving viral suppression).
Annual award amounts for years 2–5
will be set at continuation.
DATES: The period for this award will be
September 30, 2022, through September
29, 2027.
FOR FURTHER INFORMATION CONTACT:
Patrick Nadol, Center for Global Health,
Centers for Disease Control and
Prevention, U.S. Embassy Bishkek, 171
Prospect Mira, Bishkek 720016 Kyrgyz
Republic, Telephone: 800–232–6348,
Email: pen5@cdc.gov.
SUPPLEMENTARY INFORMATION: The
single-source award will allow for
implementation of high-quality care and
treatment programs with a focus on
same-day antiretroviral therapy (SD–
ART) initiation. Programs will utilize
innovative approaches to ART
adherence and participant retention; as
well as HIV testing and counseling
(HTC), and prevention programs that
focus on pre-exposure prophylaxis
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SUMMARY:
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(PrEP) and opioid substitution therapy
(OST). The key focus of the project will
be integration of the Republican AIDS
Center’s granular site management
project in PEPFAR-supported subnational units to the national scale to
improve quality of provided services to
PLHIV and institutionalize quality
management system and incorporate
into national HIV plan.
The Republican AIDS Center (RAC) is
in a unique position to conduct this
work in the Kyrgyz Republic, as it is the
leading organization responsible for
National HIV Program implementation
under the Ministry of Health and Social
Development. In the Kyrgyz Republic,
the Ministry of Health and Social
Development has mandated the RAC to
lead and coordinate the national
response to HIV/AIDS, including
developing and regulating national HIV
guidelines and policies.
Summary of the Award
Recipient: Republican AIDS Center,
Kyrgyz Republic.
Purpose of the Award: The purpose of
this award is to build on previous
PEPFAR program support to ensure
continuity of high-quality HIV services
to existing clients across the HIV
cascade and achieve the UNAIDS 95–
95–95 goals. The award will support a
comprehensive and integrated HIV
program (e.g.: Surveillance, prevention,
and treatment to prevent new
infections), improve health outcomes for
PLHIV (i.e.: Achieving and sustaining
VL suppression), reduce HIV
transmission and mortality in
accordance with KR’s national
prevention goal, and strengthen public
health functions to address other health
priorities.
Amount of Award: The approximate
year 1 funding amount will be
$2,000,000 in Federal Fiscal Year (FFY)
2022 funds, subject to the availability of
funds. Annual award amounts for years
2–5 will be set at continuation.
Authority: This program is authorized
under Public Law 108–25 (the United
States Leadership Against HIV AIDS,
Tuberculosis and Malaria Act of 2003).
Period of Performance: September 30,
2022, through September 29, 2027.
Dated: January 19, 2022.
Terrance Perry,
Chief Grants Management Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2022–01266 Filed 1–21–22; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Notice of Award of a Single-Source
Cooperative Agreement To Fund the
Vietnam Department of Animal Health
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), located
within the Department of Health and
Human Services (HHS), announces the
award of approximately $1,000,000,
with an expected total funding of
approximately $5,000,000 over a fiveyear project period, to the Vietnam
Department of Animal Health. The
award will strengthen capabilities and
maintain the government run
laboratory-supported surveillance at the
animal-human interface for avian and
non-avian influenza viruses, other
zoonotic diseases (e.g., rabies, African
Swine Fever, etc.), and other respiratory
zoonotic viruses (e.g., SARS–CoV–2) in
Vietnam.
DATES: The period for this award will be
September 30, 2022, through September
29, 2027.
FOR FURTHER INFORMATION CONTACT: Nga
Vuong, National Center for
Immunization and Respiratory Diseases,
Centers for Disease Control and
Prevention, 1600 Clifton Rd. NE, MS
H24–7, Atlanta, GA 30329, Telephone:
800–232–6348.
SUPPLEMENTARY INFORMATION: The
single-source award will strengthen
capabilities and maintain the
government run laboratory-supported
surveillance at the animal-human
interface for avian and non-avian
zoonotic influenza viruses, other
zoonotic diseases, and other respiratory
zoonotic viruses in Vietnam.
The Vietnam Department of Animal
Health (DAH) is in a unique position to
conduct this work because of their
position as the sole official, authorized
governmental agency with the legal and
regulatory authority and ability to lead
and manage animal health and pathogen
surveillance. DAH provides technical
management and oversight to its subdepartments across the country to
implement animal surveillance and
related activities such as outbreak
investigation. DAH’s 7 Regional Animal
Health Offices (RAHOs) are strategically
located throughout the country and
have in-house lab testing capacity. DAH
is at the center of a national network of
SUMMARY:
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Agencies
[Federal Register Volume 87, Number 15 (Monday, January 24, 2022)]
[Notices]
[Pages 3542-3544]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-01260]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-22-22BY; Docket No. CDC-2022-0008]
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 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 Importation Regulations (42 CFR
71 subpart F), which specifies the requirements for importing animals
or animal products that are regulated by CDC into the United States.
DATES: CDC must receive written comments on or before March 25, 2022.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2022-
0008 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 H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of 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; 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;
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
Importation Regulations (42 CFR 71 Subpart F)--New--National Center
for Emerging and Zoonotic Infectious Diseases (NCEZID), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
This is a request for a new information collection to consolidate
forms and information collections related to the importation of
animals, animal products, and human remains into one information
collection. This information collection was previously part of three
separate, OMB-approved information collections: (1) 0920-1034 (expires
3/31/2022), (2) 0920-0263 (expires 9/30/2023), and (3) 0920-0199
(expires 8/31/2024). CDC is requesting a three-year OMB clearance for
this new, combined information collection.
Section 361 of the Public Health Service Act (PHSA) (42 U.S.C. 264)
[[Page 3543]]
authorizes the Secretary of Health and Human Services to make and
enforce regulations necessary to prevent the introduction, transmission
or spread of communicable diseases from foreign countries into the
United States. The Statute, and the existing regulations governing
foreign quarantine activities (42 CFR 71), authorize quarantine
officers and other personnel to inspect and undertake necessary control
measures with respect to conveyances, persons, and shipments of animals
and etiologic agents in order to protect the public's health.
CDC regulations govern the importation of animals and animal
products capable of causing human disease. Animals that are regulated
by CDC are dogs, cats, turtles, snakes, lizards, non-human primates
(NHP), civets, African rodents, and bats. CDC controls the importation
of these animals to ensure that these animals, or animal products,
being imported into the United States meet CDC regulations. CDC does
this through a permitting process for certain animals.
On June 16, 2021 CDC published a Federal Register Notice informing
the public about a temporary suspension of dogs entering the United
States from high-risk rabies countries. The canine rabies virus variant
(CRVV) was declared eliminated in the United States in 2007. The
importation of just one dog infected with CRVV risks re-introduction of
the virus into the United States resulting in a potential public health
risk with consequent monetary cost and potential loss of human and
animal life. Since 2015 there have been four known rabid dogs imported
into the United States.
During the suspension period, CDC will issue permits for importers
with dogs who have been in a high-risk CRVV country within the last six
months and do not have a current, valid U.S.-issued rabies vaccination
certificate. Only importers who are permanently relocating to the
United States, are a US government employee traveling on official
orders, are an owner of a service dog that is trained to assist them
with a disability, are an individual importing dogs for science,
education, exhibition, or law enforcement purposes, or people who
traveled with their dog before July 31, 2021 are eligible to apply for
a permit. Dogs from CRVV-free or low risk countries and dogs with valid
U.S.-issued rabies vaccination certificates that are microchipped,
healthy, and at least six months of age do not require a permit. The
current permit application to import a dog is under collection 0920-
1034. When a dog or cat arrives at an airport and is sick or dead,
importers are required to notify CDC. There is no form for this
notification.
Other animals that require a permit, and are included in this
information collection are NHPs, which can carry of number of diseases
that can cause severe infections in people. NHPs may not be imported as
pets and may only be imported for bona fide scientific, educational, or
exhibition purposes, as defined in the regulations. Forms for the
importation of NHPs are currently under information collection 0920-
0263. These forms will move into this new information collection to
consolidate all forms related to the importation of animals or animal
products into one collection.
A new form to request a permit to import a regulated animal that is
neither a dog nor an NHP (e.g., turtles, African rodents, civets) is
included in this information collection. It also incorporates the
addition of bats, which is currently approved under OMB control number
0920-0199.
Regarding human remains, the Division of Global Migration and
Quarantine (DGMQ) works with the Division of Select Agents and Toxins
(DSAT) on the importation for human remains. DGMQ requests death
certificates from those wishing to import remains and then determines
if the importer will need a permit, which is issued by DSAT and will
remain in 0920-0199.
Lastly, people importing animal products must make a statement or
provide documentation demonstrating that the animal product is not
infectious.
CDC requests approval for an estimated 60,215 annual burden 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) hours
----------------------------------------------------------------------------------------------------------------
Dog Importers (42 CFR Dog Permit 60,000 1 60/60 60,000
71.51(c)(2), (d)). Application
Form.
NHP Importers (42 CFR 71.53).. NHP Shipment 120 1 15/60 30
Arrival
Notification
Form.
First Time NHP Importer (42 NHP Importer 15 1 120/60 30
CFR 71.53). Form.
Regulated Animal Importer (42 Other animal 2 1 30/60 1
CFR 71). import form.
Dog and Cat Importers (42 CFR Record of 43 1 60/60 43
71.51(b)(3)). sickness or
death.
Human Remains Importers (42 Provide death 50 1 15/60 13
CFR 71.55, 42 CFR 71.32). certificate.
Importer of animal products Statement or 391 1 15/60 98
(42 CFR 71.32). documentation
of non-
infectiousness.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 60,215
----------------------------------------------------------------------------------------------------------------
[[Page 3544]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-01260 Filed 1-21-22; 8:45 am]
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