Submission for OMB Review; Comment Request, 74851-74852 [2012-30390]
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Federal Register / Vol. 77, No. 243 / Tuesday, December 18, 2012 / Notices
emcdonald on DSK67QTVN1PROD with
(7) The applicability of the insured
institution’s fidelity bond coverage to
the person;
(8) The opinion or position of the
primary Federal and/or state regulator;
and
(9) Any additional factors in the
specific case that appear relevant.
The foregoing criteria will also be
applied by the FDIC to determine
whether the interests of justice are
served in seeking an exception in the
appropriate court when an application
is made to terminate the ten-year ban
prior to its expiration date.
Some applications can be approved
without an extensive review because the
person will not be in a position to
constitute any substantial risk to the
safety and soundness of the insured
institution. Persons who will occupy
clerical, maintenance, service or purely
administrative positions, generally fall
into this category. A more detailed
analysis will be performed in the case
of persons who will be in a position to
influence or control the management or
affairs of the insured institution.
Approval orders will be subject to the
condition that the person shall be
covered by a fidelity bond to the same
extent as others in similar positions. In
cases in which a waiver of the
institution filing requirement has been
granted to an individual, approval of the
application will be conditioned upon
that person disclosing the presence of
the conviction to all insured institutions
in the affairs of which he or she wishes
to participate. When deemed
appropriate, approval orders may also
be subject to the condition that the prior
consent of the FDIC will be required for
any proposed significant changes in the
person’s duties and/or responsibilities.
Such proposed changes may, in the
discretion of the Regional Director,
require a new application. In situations
in which an approval has been granted
for a person to participate in the affairs
of a particular insured institution and
subsequently seeks to participate at
another insured institution, approval
does not automatically follow. In such
cases, another application must be
submitted.
By Order of the Board of Directors.
Dated at Washington, DC, this 11th day of
December, 2012.
Federal Deposit Insurance Corporation.
Robert E. Feldman,
Executive Secretary.
[FR Doc. 2012–30351 Filed 12–17–12; 8:45 am]
15:29 Dec 17, 2012
Privacy Act of 1974; System of
Records
Federal Deposit Insurance
Corporation.
ACTION: Notice to Delete a System of
Records.
AGENCY:
In accordance with the
requirements of the Privacy Act of 1974,
as amended (Privacy Act), the Federal
Deposit Insurance Corporation (FDIC)
deletes one system of records from its
existing inventory of systems of records
subject to the Privacy Act.
DATES: Effective Date is July 23, 2012.
FOR FURTHER INFORMATION CONTACT: Gary
Jackson, Counsel, FDIC, 550 17th Street
NW., Washington, DC 20429, (703) 562–
2677.
SUPPLEMENTARY INFORMATION: The FDIC
deletes its system of records for the
Nationwide Mortgage Licensing System
and Registry, 76 FR 15309 (March 21,
2011). Section 1100 of Title X of the
Dodd-Frank Wall Street Reform and
Consumer Protection Act transferred to
the Bureau of Consumer Financial
Protection (CFPB) authority to develop
and maintain the national registration
system for residential mortgage loan
originators required by Section 1507 of
the Secure and Fair Enforcement for
Mortgage Licensing Act. The CFPB
published its own notice of the
establishment of a Privacy Act system of
records for the Nationwide Mortgage
Licensing System and Registry, 77 FR
35359 (June 13, 2012), effective as of
July 23, 2012.
The deletion is not within the
purview of subsection (r) of the Privacy
Act, which requires submission of a
report on a new or altered system of
records. The FDIC’s systems of records
notices subject to the Privacy Act have
been published in the Federal Register
and may be viewed at https://
www.fdic.gov/regulations/laws/rules/
2000-4000.html on the FDIC’s Privacy
Web page.
SUMMARY:
By order of the Board of Directors.
Dated at Washington, DC, this 11th day of
December 2012.
Robert E. Feldman,
Executive Secretary.
[FR Doc. 2012–30254 Filed 12–17–12; 8:45 am]
BILLING CODE P
FEDERAL ELECTION COMMISSION
Sunshine Act Meeting
AGENCY:
BILLING CODE 6714–01–P
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FEDERAL DEPOSIT INSURANCE
CORPORATION
Jkt 229001
PO 00000
Federal Election Commission.
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74851
Thursday, December 20,
2012 at 10:00 a.m.
PLACE: 999 E Street NW., Washington,
DC (Ninth Floor).
STATUS: This Meeting Will Be Open to
the Public.
ITEMS TO BE DISCUSSED:
Correction and Approval of the Minutes
for the Meeting of December 6, 2012;
Draft Advisory Opinion 2012–35: Global
Transaction Services Group, Inc.;
Draft Advisory Opinion 2012–37:
Yamaha Motor Corporation, U.S.A.;
Itemization of Ultimate Payee of
Committee Disbursements;
Request for Comment on the
Enforcement Process;
Election of Officers;
Future Meeting Dates;
Management and Administrative
Matters.
Individuals who plan to attend and
require special assistance, such as sign
language interpretation or other
reasonable accommodations, should
contact Shawn Woodhead Werth,
Secretary and Clerk, at (202) 694–1040,
at least 72 hours prior to the meeting
date.
PERSON TO CONTACT FOR INFORMATION:
Judith Ingram, Press Officer, Telephone:
(202) 694–1220.
DATE AND TIME:
Shawn Woodhead Werth,
Secretary and Clerk of the Commission.
[FR Doc. 2012–30492 Filed 12–14–12; 11:15 am]
BILLING CODE 6715–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Unaccompanied Refugee Minor
Placement and Outcomes Reports; ORR–
3 and ORR–4.
OMB No.: 0970–0034.
Description: The two reports collect
information necessary to administer the
Unaccompanied Refugee Minor (URM)
program. The ORR–3 (Placement
Report) is submitted to the Office of
Refugee Resettlement (ORR) by the State
agency at initial placement within 30
days of the placement, and whenever
there is a change in the child’s status,
including termination from the program,
within 60 days of the change or closure
of the case. The ORR–4 (Outcomes
Report) is submitted within
approximately 12 months of the initial
placement and each subsequent 12
months to record outcomes of the
E:\FR\FM\18DEN1.SGM
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74852
Federal Register / Vol. 77, No. 243 / Tuesday, December 18, 2012 / Notices
child’s progress toward the goals listed
in the child’s case plan and particularly
for youth 17 years of age and above
related to independent living and/or
educational plans. ORR–4 is also
submitted as a baseline report along
with the initial ORR–3 report for 17
years old and above youth, and as a
follow-up annual report for cases that
have terminated and are 17 to 21 years
old. ORR regulations at 45 CFR 400.120
describes specific URM program
reporting requirements.
Respondents: State governments.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Number of
responses per
respondent
Average burden
hours per
response
0.25 (15 Minutes).
1.5 (1 Hour and
30 Minutes).
ORR–3 ..........................................................................................................
15
75
ORR–4 ..........................................................................................................
15
119
Estimated Total Annual Burden
Hours: 2,958.75.
Additional Information: Copies of the
proposed collection may be obtained 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. All requests should be
identified by the title of the information
collection. Email address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7285,
Email:
OIRA_SUBMISSION@OMB.EOP.GOV.
Attn: Desk Officer for the
Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2012–30390 Filed 12–17–12; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
emcdonald on DSK67QTVN1PROD with
[Docket No. FDA–2012–D–1197]
Draft Guidance for Industry on
Certification of Designated Medical
Gases; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
VerDate Mar<15>2010
15:29 Dec 17, 2012
Jkt 229001
The Food and Drug
Administration (FDA) is announcing the
availability of a draft guidance for
industry entitled ‘‘Certification Process
for Designated Medical Gases.’’ This
draft guidance describes the new
certification process created by the Food
and Drug Administration Safety and
Innovation Act (FDASIA) for certain
medical gases and explains how FDA
plans to implement that process.
DATES: Although you can comment on
any guidance at any time (see 21 CFR
10.115(g)(5)), to ensure that the Agency
considers your comment on this draft
guidance before it begins work on the
final version of the guidance, submit
either electronic or written comments
on the draft guidance by February 19,
2013. Submit either electronic or
written comments concerning the
collection of information proposed in
the draft guidance and attached Form
3864 by February 19, 2013.
ADDRESSES: Submit written requests for
single copies of this draft guidance to
the Division of Drug Information, Center
for Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 2201,
Silver Spring, MD 20993–0002; or the
Communications Staff (HFV–12), Center
for Veterinary Medicine, Food and Drug
Administration, 7519 Standish Pl.,
Rockville, MD 20855. Send one selfaddressed adhesive label to assist that
office in processing your requests. See
the SUPPLEMENTARY INFORMATION section
for electronic access to the draft
guidance document.
Submit electronic comments on the
draft guidance to https://
www.regulations.gov. Submit written
comments to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Michael Folkendt, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
SUMMARY:
PO 00000
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Total burden
hours
281.25
2,677.5
Hampshire Ave., Silver Spring, MD
20993–0002, 301–796–1900; or
Germaine Connolly, Center for
Veterinary Medicine (HFV–116), Food
and Drug Administration, 7500
Standish Pl., Rockville, MD 20855,
240–276–8331.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a draft guidance for industry entitled
‘‘Certification Process for Designated
Medical Gases.’’ This guidance is
intended to help persons or entities
interested in requesting a certification
for a designated medical gas under the
new approval process for designated
medical gases created by FDASIA (Pub.
L. 112–144, 126 Stat. 993).
Title XI, subtitle B, of FDASIA added
sections 575 and 576 to the Federal
Food, Drug, and Cosmetic Act (the
FD&C Act), which created a certification
process for designated medical gases.
Specifically, section 575 provides that
oxygen, nitrogen, nitrous oxide, carbon
dioxide, helium, carbon monoxide, and
medical air are designated medical
gases. Section 576 permits any person,
beginning on January 5, 2013, to request
a certification of a medical gas for
certain indications and describes when
FDA will grant or deny these requests.
This draft guidance explains how
FDA plans to implement this new
certification process. Specifically, the
draft guidance describes the medical
gases that are eligible for certification,
who should submit a certification
request, what information should be
submitted, and how FDA will evaluate
and act on the request. The draft
guidance also describes how the new
certification requirement will be
enforced and describes FDA’s intent to
exercise enforcement discretion in
certain instances.
FDA has also developed a form to
help requestors submit their
certification requests. FDA recommends
that requestors use this form. The form
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]]>Agencies
[Federal Register Volume 77, Number 243 (Tuesday, December 18, 2012)]
[Notices]
[Pages 74851-74852]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-30390]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Unaccompanied Refugee Minor Placement and Outcomes Reports;
ORR-3 and ORR-4.
OMB No.: 0970-0034.
Description: The two reports collect information necessary to
administer the Unaccompanied Refugee Minor (URM) program. The ORR-3
(Placement Report) is submitted to the Office of Refugee Resettlement
(ORR) by the State agency at initial placement within 30 days of the
placement, and whenever there is a change in the child's status,
including termination from the program, within 60 days of the change or
closure of the case. The ORR-4 (Outcomes Report) is submitted within
approximately 12 months of the initial placement and each subsequent 12
months to record outcomes of the
[[Page 74852]]
child's progress toward the goals listed in the child's case plan and
particularly for youth 17 years of age and above related to independent
living and/or educational plans. ORR-4 is also submitted as a baseline
report along with the initial ORR-3 report for 17 years old and above
youth, and as a follow-up annual report for cases that have terminated
and are 17 to 21 years old. ORR regulations at 45 CFR 400.120 describes
specific URM program reporting requirements.
Respondents: State governments.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of
Instrument Number of responses per Average burden hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
ORR-3............................... 15 75 0.25 (15 Minutes).......... 281.25
ORR-4............................... 15 119 1.5 (1 Hour and 30 Minutes) 2,677.5
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 2,958.75.
Additional Information: Copies of the proposed collection may be
obtained 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. All
requests should be identified by the title of the information
collection. Email address: infocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect if OMB receives it within 30 days of
publication. Written comments and recommendations for the proposed
information collection should be sent directly to the following: Office
of Management and Budget, Paperwork Reduction Project, Fax: 202-395-
7285, Email: OIRA_SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for the
Administration for Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2012-30390 Filed 12-17-12; 8:45 am]
BILLING CODE 4184-01-P
