Proposed Data Collection Submitted for Public Comment and Recommendations, 45449-45451 [2018-19381]
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Federal Register / Vol. 83, No. 174 / Friday, September 7, 2018 / Notices
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[FR Doc. 2018–19418 Filed 9–6–18; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–18–0134; Docket No. CDC–2018–
0078]
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 Foreign Quarantine Regulations,
an information collection related to
illness and death reports from airplanes
and maritime vessels coming to the
United States, illness and death
investigations of travelers, and
information from importers of certain
items specified under 42 CFR 71
subpart F.
DATES: CDC must receive written
comments on or before November 6,
2018.
SUMMARY:
You may submit comments,
identified by Docket No. CDC–2018–
0078 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
ADDRESSES:
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45449
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Foreign Quarantine Regulations (42
CFR 71) (OMB Control No. 0920–0134)
(Exp 5/31/2019)—Revision—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
Section 361 of the Public Health
Service Act (PHSA) (42 U.S.C. 264)
(Attachment A1) 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. Statute and the existing
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45450
Federal Register / Vol. 83, No. 174 / Friday, September 7, 2018 / Notices
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. Other
inspection agencies, such as Customs
and Border Protection (CBP), assist
quarantine officers in public health
screening of persons, pets, and other
importations of public health
importance and make referrals to
quarantine station staff when indicated.
These practices and procedures ensure
protection against the introduction and
spread of communicable diseases into
and within the United States with a
minimum of recordkeeping and
reporting procedures, as well as a
minimum of interference with trade and
travel.
U.S. Quarantine Stations are located
at 20 ports of entry and land-border
crossings where international travelers
arrive. The jurisdiction of each station
includes air, maritime, and/or landborder ports of entry. Quarantine
Station staff work in partnership with
international, federal, state, and local
agencies and organizations to fulfill
their mission to reduce morbidity and
mortality among globally mobile
populations. This work is performed to
prevent the introduction, transmission,
and spread of communicable diseases
from foreign countries into the United
States or from one State or possession to
another State or possession. When an
illness suggestive of a communicable
disease is reported by conveyance
operators or port partners (e.g., Customs
and Border Protection), Quarantine
Officers respond to carry out an onsite
public health assessment and collect
reports of illness of each type, ILI and
others.
• For fall 2018, CDC is considering a
policy change related to requirements
for rabies vaccination documentation for
dogs coming from certain countries;
therefore, CDC is providing estimates of
burden and respondents related to
importation of dogs into the United
States.
• Revised estimates under 42 CFR
71.55, 42 CFR 71.32 Dead Bodies—
Death certificates.
• Revised estimate of the number of
requests for exemptions for importation
of African rodents.
Respondents for this information
collection request are any pilot in
command of an aircraft or maritime
vessel operator. With an ill person
meeting certain criteria, or death aboard;
any individual who is subject to federal
quarantine or isolation; any ill traveler
who is reported by the airlines, Customs
and Border Protection, or EMS to CDC
or the local public health authority that
meets the definition of ill person; and
any importer or filer who seeks to bring
certain animals, animal products, or
other CDC-regulated item into the
United States.
For most of these collections, there
are no costs to respondents other than
their time. Examinations of imported
animals is only required if the pet is ill
on arrival or if it has died during
transport. These exams are not routine.
Depending on the time of arrival, the
initial exam fee may be between $100
and $200. Rabies testing on a dog that
dies may be between $50 and $100. The
expected number of ill or dead dogs
arriving into the United States for which
CDC may require an examination is
estimated at less than 30 per year. CDC
is requesting a three-year approval.
data from the individual. This response
may occur jointly with port partners.
The collection of comprehensive,
pertinent public health information
during these responses enables
Quarantine Officers to make an accurate
public health assessment and identify
appropriate next steps. For this reason,
quarantine station staff need to
systematically interview ill travelers
and collect relevant health and
epidemiologic information.
CDC is making a number of changes
and adjustments to this information
collection. The changes are as follows:
• CDC is merging this information
collection with another, 0920–0821
Illness Response Forms: Airline,
Maritime, and Land/Border Crossing.
• CDC is disaggregating the
information collection 42 CFR 71.21(a)
report of illness or death from ships so
that the influenza like illness (ILI)
report, which is voluntary, is separate
from the required report of ill person or
death.
• CDC is removing the information
collection pertaining to Partner
Government Agency Message Sets,
because CDC will not collect
information using these tools.
• CDC is removing the acute
gastroenteritis reports from ships and
removal of medical logs information
collection from this information
collection request, because CDC’s Vessel
Sanitation Program will submit a
separate information collection request
for these tools.
CDC is requesting the following
adjustments
• As described above, CDC is
requesting a separation of the maritime
(ILI) and other maritime illness or death
reports. CDC is also requesting an
increase in the total number of maritime
ESTIMATED ANNUALIZED BURDEN HOURS
Regulatory provision or form name
Maritime Vessel Operator ......
42 CFR 71.21(a) report of illness or death from ships—Maritime
Conveyance Illness or Death Investigation Form sections 1–4.
42 CFR 71.21(a) report of illness or death from ships—Maritime
Conveyance Illness or Death Investigation Form section 5.
Cumulative Influenza/Influenza-Like Illness (ILI) ..........................
42 CFR 71.21(b) Death/Illness reports from aircrafts ..................
Airline Travel Illness or Death Investigation Form .......................
Land Travel Illness or Death Investigation Form .........................
42 CFR 71.33 Report by persons in isolation or surveillance .....
Maritime Vessel Operator ......
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Number of
respondents
Type of respondent
Maritime Vessel Operator ......
Pilot in command ...................
Traveler ..................................
Traveler ..................................
Isolated or Quarantined individuals.
Maritime Vessel Operator ......
Importer ..................................
Importer ..................................
Importer ..................................
Importer ..................................
Importer ..................................
Importer ..................................
VerDate Sep<11>2014
42 CFR 71.35 Report of death/illness during stay in port ...........
42 CFR 71.51(c)(1), (d)—Valid Rabies Vaccination Certificates
CDC Form 75.37 Notice To Owners And Importers Of Dogs:
Requirement for Dog Confinement.
42 CFR 71.51(c)(i), (ii), and (iii) exemption criteria for the importation of a dog without a rabies vaccination certificate.
42 CFR 71.51(c)(2), (d) Application For Permission To Import A
Dog Inadequately Against Rabies.
42 CFR 71.51(b)(3) Dogs/cats: Record of sickness or deaths ....
42 CFR 71.52(d) Turtle Importation Permits ................................
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Number of
responses per
respondent
Average
burden
per response
(in hours)
Total burden
hours
500
1
5/60
42
100
1
2/60
3
3,000
1,700
1,700
100
11
1
1
1
1
1
2/60
2/60
5/60
5/60
3/60
100
57
142
8
1
5
113,500
14
1
1
1
30/60
15/60
10/60
3
28,375
2
958,000
1
15/60
239,500
50
1
45/60
38
20
5
1
1
15/60
30/60
5
3
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Federal Register / Vol. 83, No. 174 / Friday, September 7, 2018 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
responses per
respondent
Average
burden
per response
(in hours)
Total burden
hours
Regulatory provision or form name
Importers ................................
Importer ..................................
Importer ..................................
Importer ..................................
42 CFR 71.55 Dead Bodies, 42 CFR 71.32—Death certificates
42 CFR 71.56 (a)(2) African Rodents—Request for exemption ..
42 CFR 71.56(a)(iii) Appeal .........................................................
42 CFR 71.32 Statements or documentation of non-infectiousness.
20
25
2
2,000
1
1
1
1
1
1
1
5/60
20
25
2
167
Total ................................
.......................................................................................................
........................
........................
........................
268,493
Jeffrey M. Zirger,
Acting Chief, Information Collection Review
Office, Office of Scientific Integrity, Office
of the Associate Director for Science, Office
of the Director, Centers for Disease Control
and Prevention.
[FR Doc. 2018–19381 Filed 9–6–18; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–18–18CI]
Agency Forms Undergoing Paperwork
Reduction Act Review
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Number of
respondents
Type of respondent
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Evaluation of
TransLife Center (TLC): A LocallyDeveloped Combination Prevention
Intervention for Transgender Women at
High Risk of HIV Infection’’ 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
30, 2018 to obtain comments from the
public and affected agencies. CDC
received one (1) 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;
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(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 or
send an email to omb@cdc.gov. 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
Evaluation of TransLife Center (TLC):
A Locally-Developed Combination
Prevention Intervention for Transgender
Women at High Risk of HIV Infection—
New—National Center for HIV/AIDS,
Viral Hepatitis, STD and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The National Center for HIV/AIDS,
Viral Hepatitis, STD and TB Prevention
is requesting approval for 24 months of
data collection entitled, ‘‘Evaluation of
TransLife Center (TLC): A LocallyDeveloped Combination Prevention
Intervention for Transgender Women at
High Risk for HIV Infection.’’ The
purpose of this study is to evaluate the
efficacy of TLC, which provides
combination (biomedical, behavioral
and social/structural) HIV prevention
and care services to adult transgender
women at high risk for HIV infection, in
a culturally specific and accessible
environment. The information collected
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through this study will be used to
evaluate whether the TLC intervention
is an effective HIV-prevention strategy
by assessing whether exposure to TLC
services results in improvements in
participants’ health and HIV prevention
behaviors. The trial will assess whether
intervention participants’ behaviors
significantly change from baseline to 4and 8-month follow-up periods.
This study will be carried out in
Chicago, Illinois, where the TLC
program is located. The study
population will include 150 HIVnegative adult transgender women
living in the Chicago metropolitan area.
Participants will be at least 18 years of
age; self-identify as transgender,
transsexual, women and/or female who
was assigned male sex at birth; and have
a self-reported history of sex with men
in the past four months. The study
population will also include 10 TLC
staff members. Staff members will be
adults, involved in the delivery of TLC
intervention services. Participation in
this study is voluntary.
We anticipate enrollment of a diverse
sample of transgender women
comprised mainly of racial/ethnic
minority participants under 35 years of
age, consistent with the current TLC
program and the epidemiology of HIV
infection among transgender women.
Intervention participants will be
recruited to the study through a
combination of approaches, including
traditional print advertisement, referral,
in-person outreach, and through word of
mouth. TLC staff members will be
randomly selected to participate in the
evaluation.
A computer-assisted quantitative
assessment will be used to collect
information for this study, which will
be delivered at the time of study
enrollment and again at 4-month and 8month follow-ups. The assessment will
be used to measure changes in sexual
risk behavior including condom use and
pre-exposure prophylaxis (PrEP) care
engagement. Intervention mediators,
including gender affirmation, collective
self-esteem and social support, and
intervention satisfaction will also be
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]]>Agencies
[Federal Register Volume 83, Number 174 (Friday, September 7, 2018)]
[Notices]
[Pages 45449-45451]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-19381]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-18-0134; Docket No. CDC-2018-0078]
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 Foreign Quarantine Regulations,
an information collection related to illness and death reports from
airplanes and maritime vessels coming to the United States, illness and
death investigations of travelers, and information from importers of
certain items specified under 42 CFR 71 subpart F.
DATES: CDC must receive written comments on or before November 6, 2018.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2018-
0078 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
[email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
Foreign Quarantine Regulations (42 CFR 71) (OMB Control No. 0920-
0134) (Exp 5/31/2019)--Revision--National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Section 361 of the Public Health Service Act (PHSA) (42 U.S.C. 264)
(Attachment A1) 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. Statute and the existing
[[Page 45450]]
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. Other inspection agencies, such as Customs
and Border Protection (CBP), assist quarantine officers in public
health screening of persons, pets, and other importations of public
health importance and make referrals to quarantine station staff when
indicated. These practices and procedures ensure protection against the
introduction and spread of communicable diseases into and within the
United States with a minimum of recordkeeping and reporting procedures,
as well as a minimum of interference with trade and travel.
U.S. Quarantine Stations are located at 20 ports of entry and land-
border crossings where international travelers arrive. The jurisdiction
of each station includes air, maritime, and/or land-border ports of
entry. Quarantine Station staff work in partnership with international,
federal, state, and local agencies and organizations to fulfill their
mission to reduce morbidity and mortality among globally mobile
populations. This work is performed to prevent the introduction,
transmission, and spread of communicable diseases from foreign
countries into the United States or from one State or possession to
another State or possession. When an illness suggestive of a
communicable disease is reported by conveyance operators or port
partners (e.g., Customs and Border Protection), Quarantine Officers
respond to carry out an onsite public health assessment and collect
data from the individual. This response may occur jointly with port
partners. The collection of comprehensive, pertinent public health
information during these responses enables Quarantine Officers to make
an accurate public health assessment and identify appropriate next
steps. For this reason, quarantine station staff need to systematically
interview ill travelers and collect relevant health and epidemiologic
information.
CDC is making a number of changes and adjustments to this
information collection. The changes are as follows:
CDC is merging this information collection with another,
0920-0821 Illness Response Forms: Airline, Maritime, and Land/Border
Crossing.
CDC is disaggregating the information collection 42 CFR
71.21(a) report of illness or death from ships so that the influenza
like illness (ILI) report, which is voluntary, is separate from the
required report of ill person or death.
CDC is removing the information collection pertaining to
Partner Government Agency Message Sets, because CDC will not collect
information using these tools.
CDC is removing the acute gastroenteritis reports from
ships and removal of medical logs information collection from this
information collection request, because CDC's Vessel Sanitation Program
will submit a separate information collection request for these tools.
CDC is requesting the following adjustments
As described above, CDC is requesting a separation of the
maritime (ILI) and other maritime illness or death reports. CDC is also
requesting an increase in the total number of maritime reports of
illness of each type, ILI and others.
For fall 2018, CDC is considering a policy change related
to requirements for rabies vaccination documentation for dogs coming
from certain countries; therefore, CDC is providing estimates of burden
and respondents related to importation of dogs into the United States.
Revised estimates under 42 CFR 71.55, 42 CFR 71.32 Dead
Bodies--Death certificates.
Revised estimate of the number of requests for exemptions
for importation of African rodents.
Respondents for this information collection request are any pilot
in command of an aircraft or maritime vessel operator. With an ill
person meeting certain criteria, or death aboard; any individual who is
subject to federal quarantine or isolation; any ill traveler who is
reported by the airlines, Customs and Border Protection, or EMS to CDC
or the local public health authority that meets the definition of ill
person; and any importer or filer who seeks to bring certain animals,
animal products, or other CDC-regulated item into the United States.
For most of these collections, there are no costs to respondents
other than their time. Examinations of imported animals is only
required if the pet is ill on arrival or if it has died during
transport. These exams are not routine. Depending on the time of
arrival, the initial exam fee may be between $100 and $200. Rabies
testing on a dog that dies may be between $50 and $100. The expected
number of ill or dead dogs arriving into the United States for which
CDC may require an examination is estimated at less than 30 per year.
CDC is requesting a three-year approval.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Regulatory provision or form name Number of responses per per response Total burden
respondents respondent (in hours) hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Maritime Vessel Operator.................. 42 CFR 71.21(a) report of illness or death 500 1 5/60 42
from ships--Maritime Conveyance Illness or
Death Investigation Form sections 1-4.
Maritime Vessel Operator.................. 42 CFR 71.21(a) report of illness or death 100 1 2/60 3
from ships--Maritime Conveyance Illness or
Death Investigation Form section 5.
Maritime Vessel Operator.................. Cumulative Influenza/Influenza-Like Illness 3,000 1 2/60 100
(ILI).
Pilot in command.......................... 42 CFR 71.21(b) Death/Illness reports from 1,700 1 2/60 57
aircrafts.
Traveler.................................. Airline Travel Illness or Death 1,700 1 5/60 142
Investigation Form.
Traveler.................................. Land Travel Illness or Death Investigation 100 1 5/60 8
Form.
Isolated or Quarantined individuals....... 42 CFR 71.33 Report by persons in isolation 11 1 3/60 1
or surveillance.
Maritime Vessel Operator.................. 42 CFR 71.35 Report of death/illness during 5 1 30/60 3
stay in port.
Importer.................................. 42 CFR 71.51(c)(1), (d)--Valid Rabies 113,500 1 15/60 28,375
Vaccination Certificates.
Importer.................................. CDC Form 75.37 Notice To Owners And 14 1 10/60 2
Importers Of Dogs: Requirement for Dog
Confinement.
Importer.................................. 42 CFR 71.51(c)(i), (ii), and (iii) 958,000 1 15/60 239,500
exemption criteria for the importation of a
dog without a rabies vaccination
certificate.
Importer.................................. 42 CFR 71.51(c)(2), (d) Application For 50 1 45/60 38
Permission To Import A Dog Inadequately
Against Rabies.
Importer.................................. 42 CFR 71.51(b)(3) Dogs/cats: Record of 20 1 15/60 5
sickness or deaths.
Importer.................................. 42 CFR 71.52(d) Turtle Importation Permits.. 5 1 30/60 3
[[Page 45451]]
Importers................................. 42 CFR 71.55 Dead Bodies, 42 CFR 71.32-- 20 1 1 20
Death certificates.
Importer.................................. 42 CFR 71.56 (a)(2) African Rodents--Request 25 1 1 25
for exemption.
Importer.................................. 42 CFR 71.56(a)(iii) Appeal................. 2 1 1 2
Importer.................................. 42 CFR 71.32 Statements or documentation of 2,000 1 5/60 167
non-infectiousness.
---------------------------------------------------------------
Total................................. ............................................ .............. .............. .............. 268,493
--------------------------------------------------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Acting Chief, Information Collection Review Office, Office of
Scientific Integrity, Office of the Associate Director for Science,
Office of the Director, Centers for Disease Control and Prevention.
[FR Doc. 2018-19381 Filed 9-6-18; 8:45 am]
BILLING CODE 4163-18-P
