Proposed Information Collection Activity; Comment Request, 32875-32877 [2018-15149]
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Federal Register / Vol. 83, No. 136 / Monday, July 16, 2018 / Notices
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. The term ‘‘collection of
information’’ is defined in 44 U.S.C.
3502(3) and 5 CFR 1320.3(c) and
includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension or
reinstatement of an existing collection
of information, before submitting the
collection to OMB for approval. To
comply with this requirement, CMS is
publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: New collection (Request for a
new OMB control number); Title of
Information Collection: Health Equity
Technical Assistance Monitoring and
Tracking; Use: The Centers for Medicare
& Medicaid Services (CMS) Office of
Minority Health (OMH) developed the
CMS Equity Plan for Improving Quality
in Medicare (CMS Equity Plan for
Medicare). The Plan outlines CMS’ path
to help advance health equity by
improving the quality of care provided
to minority and other underserved
Medicare beneficiaries, particularly
those with disparities in chronic
diseases. CMS identified six highimpact priority areas based on a review
of the evidence base and stakeholder
input. These priorities encompass both
system- and community-level
approaches to achieve equity in
Medicare. Priority 2: Evaluate
Disparities Impacts and Integrate Equity
Solutions Across CMS Programs,
focuses on increasing understanding of
the impact CMS programs have on
health disparities and on identifying,
developing and integrating proven
solutions to improve their impact on
vulnerable populations.
CMS created a Health Equity
Technical Assistance (TA) email
(HealthEquityTA@cms.hhs.gov) to
support CMS programs as they integrate
health equity into their programs. This
TA offers guidance from health equity
subject matter experts on a variety of
topics including reviewing data to
identify health disparities, identifying
root causes of health disparities, gaining
an organizational champion, building
organizational capacity to address
health disparities, implementing
interventions, tracking success of
intervention, and serves as a portal to
VerDate Sep<11>2014
17:31 Jul 13, 2018
Jkt 244001
access health equity resources. Form
Number: CMS–10669 (OMB control
number: 0938—New); Frequency:
Occasionally; Affected Public: Private
sector (Business or other For-profits);
Number of Respondents: 274; Total
Annual Responses 274; Total Annual
Hours: 23. (For policy questions
regarding this collection contact
Alexandra Bryden at 410–786–2076).
Dated: July 11, 2018.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2018–15146 Filed 7–13–18; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: U.S. Repatriation Program
Forms.
OMB No.: 0970—NEW (two of the
forms have prior OMB No: [SSA–3955 &
SSA–2061])
Description: The United States (U.S.)
Repatriation Program was established by
Title XI, Section 1113 of the Social
Security Act (Assistance for U.S.
Citizens Returned from Foreign
Countries) to provide temporary
assistance to U.S. citizens and their
dependents who have been identified by
the Department of State (DOS) as having
returned, or been brought from a foreign
country to the U.S. because of
destitution, illness, war, threat of war,
or a similar crisis, and are without
available resources immediately
accessible to meet their needs. The
Secretary of the Department of Health
and Human Services (HHS) was
provided with the authority to
administer this Program. On or about
1994, this authority was delegated by
the HHS Secretary to the Administration
for Children and Families (ACF) and
later re-delegated by ACf to the Office of
Refugee Resettlement. The Repatriation
Program works with States, Federal
agencies, and non-governmental
organizations to provide eligible
individuals with temporary assistance
for up to 90-days. This assistance is in
the form of a loan and must be repaid
to the Federal Government.
The Program was later expanded in
response to legislation enacted by
Congress to address the particular needs
of persons with mental illness (24
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
32875
U.S.C. Sections 321 through 329).
Further refinements occurred in
response to Executive Order (E.O.)
11490 (as amended) where HHS was
given the responsibility to ‘‘develop
plans and procedures for assistance at
ports of entry to U.S. personnel
evacuated from overseas areas, their
onward movement to final destination,
and follow-up assistance after arrival at
final destination.’’ In addition, under
E.O. 12656 (53 CFR 47491),
‘‘Assignment of emergency
preparedness responsibilities,’’ HHS
was given the lead responsibility to
develop plans and procedures in order
to provide assistance to U.S. citizens
and others evacuated from overseas
areas.
Overall, the Program manages two
major activities, Emergency and Nonemergency Repatriation Activities. The
ongoing routine arrivals of individual
repatriates and the repatriation of
individuals with mental illness
constitute the Program Non-emergency
activities. Emergency activities are
comprised of group repatriations
(evacuations of 50–500 individuals) and
emergency repatriations (evacuations of
500 or more individuals). Operationally,
these activities involve different kinds
of preparation, resources, and
implementation. However, the core
Program policies and administrative
procedures are essentially the same. The
Program provides services through
agreements with local repatriation
service providers (e.g. States, federal
agencies, non-governmental agencies,
etc.). For the purpose of this Program,
local repatriation service provider (local
provider) has the same definition of
‘‘agency’’ as defined under 45 CFR 212.1
(i).
1. The HHS Repatriation Program
Emergency and Group Processing Form:
Under 45 CFR 211 and 212, ORR is to
make findings setting forth the pertinent
facts and conclusions according to
established standards to determine
whether an individual is an eligible
person. This form allows authorized
staff to gather necessary information to
determine eligibility and needed
services. This form is to be utilized
during emergencies and group
repatriations. Individuals interested in
receiving Repatriation assistance will
complete appropriate portions of this
form. State personnel will utilize this
form as a guide to perform an initial
eligibility and needs assessment. An
authorized federal staff from the ACF
will make final eligibility
determinations through the approval of
this form.
2. The U.S. Repatriation Program
Privacy and Repayment Agreement
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Federal Register / Vol. 83, No. 136 / Monday, July 16, 2018 / Notices
Form: Under 45 CFR 211 and 212,
individuals who receive Program
assistance are required to repay the
federal government for the cost
associated to the services received. This
form authorizes ORR to release personal
identifiable information to partners for
the purpose of providing services to
eligible repatriates. In addition, through
this form, eligible repatriates agree to
accept services under the terms and
conditions of the Program. Specifically,
eligible repatriates commit to repay the
federal government for all services
received while in the Program. This
form is to be completed by eligible
repatriates or authorized legal
custodian. Exception applies to
unaccompanied minors and individuals
eligible under 45 CFR 211, if no legal
custodian is identified.
3. Relinquish Repatriation Services
Form: For individuals who are eligible
to receive repatriation assistance but opt
to relinquish services, this form is
utilized to confirm and record
repatriate’s decision to refuse Program
assistance. This form is to be completed
by eligible repatriates or authorized
legal custodian. Exception applies to
unaccompanied minors and individuals
eligible under 45 CFR 211, if no legal
custodian is identified.
4. The U.S. Repatriation Program
Emergency Financial Form: Under
Section 1113 of the Social Security Act,
ORR is authorized to provide temporary
assistance directly or through utilization
of the services and facilities of
appropriate public or private agencies
and organizations, in accordance with
agreements providing for payment, as
may be determined by ORR. This form
is to be utilized and completed by ORR
local providers to request
reimbursement of reasonable and
allowable costs, both administrative and
actual temporary services, after
emergency activities.
5. The U.S. Repatriation Program
Non-emergency Reimbursement Form:
Under Section 1113 of the Social
Security Act, ORR is authorized to
provide temporary assistance directly or
through arrangements, in accordance
with agreements providing for payment,
as may be determined by ORR. This
form is to be utilized and completed by
ORR local providers to request
reimbursement of reasonable and
allowable costs, both administrative and
actual temporary services.
6. The U.S. Repatriation Program
Financial Waiver Request Form: In
accordance with 45 CFR 211 & 212
individuals who have received
Repatriation assistance may be eligible
to receive a waiver or deferral of their
repatriation loan. This form is to be
completed by eligible repatriates,
authorized legal custodian, or the
repatriation local provider. Exception
applies to unaccompanied minors and
individuals eligible under 45 CFR 211,
if no legal custodian is identified.
7. The U.S. Repatriation Program
Temporary Assistance Extension
Request Form: Under 45 CFR 211 & 212
temporary assistance may be furnished
beyond the 90 days eligibility period.
This form is to be completed by the
eligible repatriates, authorized legal
custodian, or the repatriation local
provider. This form should be submitted
to ORR or its authorized grantee 14 days
prior to the expiration of the 90 days
eligibility period.
8. The U.S. Repatriation Program
Individual Case Management Report
and Financial Claim Form: Under
Section 1113 of the Social Security Act,
ORR is authorized to provide temporary
assistance directly or through
agreements with public and private
agencies. This form is to be utilized and
completed by ORR local provider to
request reimbursement of reasonable
and allowable costs, both administrative
and actual temporary services. This
form should also be utilized by the local
repatriation provider for submit case
updates. This forms is to be completed
by authorized local providers.
Respondents: Repatriation Program
local repatriation service provider and
individuals repatriated or evacuated by
DOS from overseas. These respondents
are authorized under Title XI, Section
1113 of the Social Security Act (42
U.S.C. 1313), Executive Order 12656
(amended by E.O. 13074, February 9,
1998; E.O. 13228, October 8, 2001; E.O.
13286, February 28, 2003), and 45 CFR
211 & 212.
ANNUAL BURDEN ESTIMATES
Number of
responses per
respondent
Average
burden hours
per response
Number of
respondents
U.S. Repatriation Program Emergency and Group Processing Form ...
U.S. Repatriation Program Privacy and Repayment Agreement Form:
U.S. Repatriation Program Relinquish Temporary Assistance Form .....
U.S. Repatriation Program Emergency and Group Financial Form .......
U.S. Repatriation Program Non-emergency Monthly Financial Statement Form.
U.S. Repatriation Program Loan Waiver Request Form ........................
U.S. Repatriation Program Temporary Assistance Extension Request
Form.
U.S. Repatriation Program Individual Case Management Report .........
sradovich on DSK3GMQ082PROD with NOTICES
Instrument
500 or more ......
1000 or more ....
50 or more ........
4 or more ..........
53 or more ........
1
1
1
1
1
.......................
.......................
.......................
.......................
.......................
0.15
0.05
0.05
.20
0.20
75 or more.
50 or more.
0.8 or more.
4 or more.
10.6 or more.
100 or more ......
500 or more ......
1 .......................
1 .......................
1
0.20
100 or more.
100 or more.
1000 or more ....
1 or more ..........
0.20
200 or more.
Estimated Total Annual Burden
Hours: 540.4.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
VerDate Sep<11>2014
17:31 Jul 13, 2018
Jkt 244001
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW, Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
Email address: infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
PO 00000
Frm 00045
Fmt 4703
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Total burden
hours
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
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Federal Register / Vol. 83, No. 136 / Monday, July 16, 2018 / Notices
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2018–15149 Filed 7–13–18; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–N–0341]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; New Animal Drugs
for Investigational Use
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
SUMMARY:
Fax written comments on the
collection of information by August 15,
2018.
DATES:
To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, Fax: 202–
395–7285, or emailed to oira_
submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0117. Also
include the FDA docket number found
in brackets in the heading of this
document.
ADDRESSES:
sradovich on DSK3GMQ082PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
Amber Sanford, Office of Operations,
Food and Drug Administration, Three
White Flint North, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–8867, PRAStaff@
fda.hhs.gov.
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
17:31 Jul 13, 2018
Jkt 244001
New Animal Drugs for Investigational
Use
OMB Control Number 0910–0117—
Extension
FDA has the authority under the
Federal Food, Drug, and Cosmetic Act
(FD&C Act) to approve new animal
drugs. A new animal drug application
(NADA) cannot be approved until,
among other things, the new animal
drug has been demonstrated to be safe
and effective for its intended use(s). In
order to properly test a new animal drug
for an intended use, appropriate
scientific investigations must be
conducted. Under specific
circumstances, section 512(j) of the
FD&C Act (21 U.S.C. 360b(j)) permits
the use of an investigational new animal
drug to generate data to support an
NADA approval. Section 512(j) of the
FD&C Act authorizes us to issue
regulations relating to the
investigational use of new animal drugs.
Our regulations in 21 CFR part 511 set
forth the conditions for investigational
use of new animal drugs and require
reporting and recordkeeping. The
information collected is necessary to
protect the public health. We use the
information to determine that
investigational animal drugs are
distributed only to qualified
investigators, adequate drug
accountability records are maintained,
and edible food products from treated
food-producing animals are safe for
human consumption. We also use the
information collected to monitor the
validity of the studies submitted to us
to support new animal drug approval.
Reporting: Our regulations require
that certain information be submitted to
us in a ‘‘Notice of Claimed
Investigational Exemption for a New
Animal Drug’’ (NCIE) to qualify for the
exemption and to control shipment of
the new animal drug and prevent
potential abuse. The NCIE must contain,
among other things, the following
specific information: (1) Identity of the
new animal drug, (2) labeling, (3)
statement of compliance of any
nonclinical laboratory studies with good
laboratory practices, (4) name and
address of each clinical investigator, (5)
the approximate number of animals to
be treated or amount of new animal
drug(s) to be shipped, and (6)
information regarding the use of edible
tissues from investigational animals
(§ 511.1(b)(4) (21 CFR 511.1(b)(4)). If the
new animal drug is to be used in foodproducing animals, e.g., cattle, swine,
chickens, fish, etc., certain data must be
submitted to us to obtain authorization
for the use of edible food products from
treated food-producing animals
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Sfmt 4703
32877
(§ 511.1(b)(5)). We require sponsors
upon request to submit information
with respect to the investigation to
determine whether there are grounds for
terminating the exemption
(§ 511.1(b)(6)). We require sponsors to
report findings that may suggest
significant hazards pertinent to the
safety of the new animal drug
(§ 511.1(b)(8)(ii)). We also require
reporting by importers of investigational
new animal drugs for clinical
investigational use in animals
(§ 511.1(b)(9)). The information
provided by the sponsor in the NCIE is
needed to ensure that the proposed
investigational use of the new animal
drug is safe and that any edible food
will not be distributed without proper
authorization from FDA. Information
contained in an NCIE submission is
monitored under our Bio-Research
Monitoring Program. This program
permits us to monitor the validity of the
studies and to ensure the proper use of
the drugs is maintained by the
investigators.
Recordkeeping: If the new animal
drug is only for tests in vitro or in
laboratory research animals, the person
distributing the new animal drug must
maintain records showing the name and
post office address of the expert or
expert organization to whom it is
shipped and the date, quantity, and
batch or code mark of each shipment
and delivery for a period of 2 years after
such shipment or delivery (§ 511.1(a)(3)
and (b)(3)). We require complete records
of the investigation, including records of
the receipt and disposition of each
shipment or delivery of the
investigational new animal drug
(§ 511.1(b)(7)). We also require records
of all reports received by a sponsor from
investigators to be retained for 2 years
after the termination of an
investigational exemption or approval of
a new animal drug application
(§ 511.1(b)(8)(i)).
Description of Respondents:
Respondents to this collection of
information are persons who use new
animal drugs for investigational
purposes. Investigational new animal
drugs are used primarily by drug
industry firms, academic institutions,
and the government. Investigators may
include individuals from these entities,
as well as research firms and members
of the medical professions.
In the Federal Register of February
22, 2018 (83 FR 7735), FDA published
a 60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
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]]>Agencies
[Federal Register Volume 83, Number 136 (Monday, July 16, 2018)]
[Notices]
[Pages 32875-32877]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-15149]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: U.S. Repatriation Program Forms.
OMB No.: 0970--NEW (two of the forms have prior OMB No: [SSA-3955 &
SSA-2061])
Description: The United States (U.S.) Repatriation Program was
established by Title XI, Section 1113 of the Social Security Act
(Assistance for U.S. Citizens Returned from Foreign Countries) to
provide temporary assistance to U.S. citizens and their dependents who
have been identified by the Department of State (DOS) as having
returned, or been brought from a foreign country to the U.S. because of
destitution, illness, war, threat of war, or a similar crisis, and are
without available resources immediately accessible to meet their needs.
The Secretary of the Department of Health and Human Services (HHS) was
provided with the authority to administer this Program. On or about
1994, this authority was delegated by the HHS Secretary to the
Administration for Children and Families (ACF) and later re-delegated
by ACf to the Office of Refugee Resettlement. The Repatriation Program
works with States, Federal agencies, and non-governmental organizations
to provide eligible individuals with temporary assistance for up to 90-
days. This assistance is in the form of a loan and must be repaid to
the Federal Government.
The Program was later expanded in response to legislation enacted
by Congress to address the particular needs of persons with mental
illness (24 U.S.C. Sections 321 through 329). Further refinements
occurred in response to Executive Order (E.O.) 11490 (as amended) where
HHS was given the responsibility to ``develop plans and procedures for
assistance at ports of entry to U.S. personnel evacuated from overseas
areas, their onward movement to final destination, and follow-up
assistance after arrival at final destination.'' In addition, under
E.O. 12656 (53 CFR 47491), ``Assignment of emergency preparedness
responsibilities,'' HHS was given the lead responsibility to develop
plans and procedures in order to provide assistance to U.S. citizens
and others evacuated from overseas areas.
Overall, the Program manages two major activities, Emergency and
Non-emergency Repatriation Activities. The ongoing routine arrivals of
individual repatriates and the repatriation of individuals with mental
illness constitute the Program Non-emergency activities. Emergency
activities are comprised of group repatriations (evacuations of 50-500
individuals) and emergency repatriations (evacuations of 500 or more
individuals). Operationally, these activities involve different kinds
of preparation, resources, and implementation. However, the core
Program policies and administrative procedures are essentially the
same. The Program provides services through agreements with local
repatriation service providers (e.g. States, federal agencies, non-
governmental agencies, etc.). For the purpose of this Program, local
repatriation service provider (local provider) has the same definition
of ``agency'' as defined under 45 CFR 212.1 (i).
1. The HHS Repatriation Program Emergency and Group Processing
Form: Under 45 CFR 211 and 212, ORR is to make findings setting forth
the pertinent facts and conclusions according to established standards
to determine whether an individual is an eligible person. This form
allows authorized staff to gather necessary information to determine
eligibility and needed services. This form is to be utilized during
emergencies and group repatriations. Individuals interested in
receiving Repatriation assistance will complete appropriate portions of
this form. State personnel will utilize this form as a guide to perform
an initial eligibility and needs assessment. An authorized federal
staff from the ACF will make final eligibility determinations through
the approval of this form.
2. The U.S. Repatriation Program Privacy and Repayment Agreement
[[Page 32876]]
Form: Under 45 CFR 211 and 212, individuals who receive Program
assistance are required to repay the federal government for the cost
associated to the services received. This form authorizes ORR to
release personal identifiable information to partners for the purpose
of providing services to eligible repatriates. In addition, through
this form, eligible repatriates agree to accept services under the
terms and conditions of the Program. Specifically, eligible repatriates
commit to repay the federal government for all services received while
in the Program. This form is to be completed by eligible repatriates or
authorized legal custodian. Exception applies to unaccompanied minors
and individuals eligible under 45 CFR 211, if no legal custodian is
identified.
3. Relinquish Repatriation Services Form: For individuals who are
eligible to receive repatriation assistance but opt to relinquish
services, this form is utilized to confirm and record repatriate's
decision to refuse Program assistance. This form is to be completed by
eligible repatriates or authorized legal custodian. Exception applies
to unaccompanied minors and individuals eligible under 45 CFR 211, if
no legal custodian is identified.
4. The U.S. Repatriation Program Emergency Financial Form: Under
Section 1113 of the Social Security Act, ORR is authorized to provide
temporary assistance directly or through utilization of the services
and facilities of appropriate public or private agencies and
organizations, in accordance with agreements providing for payment, as
may be determined by ORR. This form is to be utilized and completed by
ORR local providers to request reimbursement of reasonable and
allowable costs, both administrative and actual temporary services,
after emergency activities.
5. The U.S. Repatriation Program Non-emergency Reimbursement Form:
Under Section 1113 of the Social Security Act, ORR is authorized to
provide temporary assistance directly or through arrangements, in
accordance with agreements providing for payment, as may be determined
by ORR. This form is to be utilized and completed by ORR local
providers to request reimbursement of reasonable and allowable costs,
both administrative and actual temporary services.
6. The U.S. Repatriation Program Financial Waiver Request Form: In
accordance with 45 CFR 211 & 212 individuals who have received
Repatriation assistance may be eligible to receive a waiver or deferral
of their repatriation loan. This form is to be completed by eligible
repatriates, authorized legal custodian, or the repatriation local
provider. Exception applies to unaccompanied minors and individuals
eligible under 45 CFR 211, if no legal custodian is identified.
7. The U.S. Repatriation Program Temporary Assistance Extension
Request Form: Under 45 CFR 211 & 212 temporary assistance may be
furnished beyond the 90 days eligibility period. This form is to be
completed by the eligible repatriates, authorized legal custodian, or
the repatriation local provider. This form should be submitted to ORR
or its authorized grantee 14 days prior to the expiration of the 90
days eligibility period.
8. The U.S. Repatriation Program Individual Case Management Report
and Financial Claim Form: Under Section 1113 of the Social Security
Act, ORR is authorized to provide temporary assistance directly or
through agreements with public and private agencies. This form is to be
utilized and completed by ORR local provider to request reimbursement
of reasonable and allowable costs, both administrative and actual
temporary services. This form should also be utilized by the local
repatriation provider for submit case updates. This forms is to be
completed by authorized local providers.
Respondents: Repatriation Program local repatriation service
provider and individuals repatriated or evacuated by DOS from overseas.
These respondents are authorized under Title XI, Section 1113 of the
Social Security Act (42 U.S.C. 1313), Executive Order 12656 (amended by
E.O. 13074, February 9, 1998; E.O. 13228, October 8, 2001; E.O. 13286,
February 28, 2003), and 45 CFR 211 & 212.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Average burden
Instrument Number of respondents Number of responses hours per Total burden hours
per respondent response
----------------------------------------------------------------------------------------------------------------
U.S. Repatriation Program 500 or more.......... 1................... 0.15 75 or more.
Emergency and Group
Processing Form.
U.S. Repatriation Program 1000 or more......... 1................... 0.05 50 or more.
Privacy and Repayment
Agreement Form:.
U.S. Repatriation Program 50 or more........... 1................... 0.05 0.8 or more.
Relinquish Temporary
Assistance Form.
U.S. Repatriation Program 4 or more............ 1................... .20 4 or more.
Emergency and Group
Financial Form.
U.S. Repatriation Program Non- 53 or more........... 1................... 0.20 10.6 or more.
emergency Monthly Financial
Statement Form.
U.S. Repatriation Program 100 or more.......... 1................... 1 100 or more.
Loan Waiver Request Form.
U.S. Repatriation Program 500 or more.......... 1................... 0.20 100 or more.
Temporary Assistance
Extension Request Form.
U.S. Repatriation Program 1000 or more......... 1 or more........... 0.20 200 or more.
Individual Case Management
Report.
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 540.4.
In compliance with the requirements of Section 506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Planning, Research and Evaluation, 370 L'Enfant Promenade SW,
Washington, DC 20447, Attn: ACF Reports Clearance Officer. Email
address: [email protected]. All requests should be identified
by the title of the information collection.
The Department specifically requests comments on: (a) Whether the
proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden information to be
collected; and (d) ways to minimize the burden of the collection of
information on
[[Page 32877]]
respondents, including through the use of automated collection
techniques or other forms of information technology. Consideration will
be given to comments and suggestions submitted within 60 days of this
publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2018-15149 Filed 7-13-18; 8:45 am]
BILLING CODE 4184-01-P
