Joint Biomedical Laboratory Research and Development and Clinical Science Research and Development Services Scientific Merit Review Board; Notice of Meeting, 34418-34419 [06-5352]
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Federal Register / Vol. 71, No. 114 / Wednesday, June 14, 2006 / Notices
equivalency deposits on the depository
bank’s books and records.
• The funds deposited and
obligations that are placed in
safekeeping at a depository bank to
satisfy a foreign bank’s capital
equivalency deposit requirement must
be maintained pursuant to an agreement
prescribed by the OCC that shall be a
written agreement entered into with the
OCC.
Maintenance of capital equivalency
ledger account: Each Federal branch or
agency shall maintain a capital
equivalency account and keep records
of the amount of liabilities requiring
capital equivalency coverage in a
manner and form prescribed by the
OCC.
12 CFR 28.15(d)(1) Capital
Equivalency Deposits—Deposit
Arrangements: A foreign bank’s capital
equivalency deposits may not be
reduced in value below the minimum
required for that branch or agency
without the prior approval of the OCC,
but in no event below the statutory
minimum.
12 CFR 28.16(c) Deposit-taking by an
Uninsured Federal branch—Application
for an Exemption: A foreign bank may
apply to the OCC for an exemption to
permit an uninsured Federal branch to
accept or maintain deposit accounts that
are not listed in paragraph (b) of this
section. The request should describe:
• The types, sources, and estimated
amount of such deposits and explain
why the OCC should grant an
exemption;
• How the exemption maintains and
furthers the policies described in
paragraph (a) of this section.
12 CFR 28.16(d) Deposit taking by an
uninsured Federal branch—Aggregation
of deposits: A foreign bank that has
more than one Federal branch in the
same state may aggregate deposits in all
of its Federal branches in that state, but
exclude deposits of other branches,
agencies or wholly owned subsidiaries
of the bank. The Federal branch shall
compute the average amount by using
the sum of deposits as of the close of
business of the last 30 calendar days
ending with and including the last day
of the calendar quarter, divided by 30.
The Federal branch shall maintain
records of the calculation until its next
examination by the OCC.
12 CFR 28.17 Covered under
Information Collection 1557–0014
(Comptroller’s Licensing Manual) Notice
of Change in Activity or Operations: A
Federal branch or agency shall notify
the OCC if it changes its corporate title;
changes its mailing address; converts to
a state branch, state agency, or
representative office; or the parent
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foreign bank changes the designation of
its home state.
12 CFR 28.18(c)(1) Recordkeeping and
Reporting—Maintenance of Accounts,
Books, and Records: Each Federal
branch or agency shall maintain a set of
accounts and records reflecting its
transactions that are separate from those
of the foreign bank and any other branch
or agency. The Federal branch or agency
shall keep a set of accounts and records
in English sufficient to permit the OCC
to examine the condition of the Federal
branch or agency and its compliance
with applicable laws and regulations.
28.20(a)(1) Maintenance of Assets—
General Rule: The OCC may require a
foreign bank to hold certain assets, with
the approval of the OCC, in the state in
which its Federal branch or agency is
located.
12 CFR 28.22 (b) Covered under
Information Collection 1557–0014
(Comptroller’s Licensing Manual)
Voluntary Liquidation: Notice to
customers and creditors—A foreign
bank shall publish notice of the
impending closure of each Federal
branch or agency for a period of two
months in every issue of a local
newspaper where the Federal branch or
agency is located. If only weekly
publication is available, the notice must
be published for nine consecutive
weeks.
12 CFR 28.22(e) Reports of
Examination: The Federal branch or
agency shall send the OCC certification
that all of its Reports of Examination
have been destroyed or return its
Reports of Examination to the OCC.
12 CFR 28.25(a) Covered under
Information Collection 1557–0014
(Comptroller’s Licensing Manual)
Change in Control—After-the-fact
Notice: A foreign bank that operates a
Federal branch or agency shall inform
the OCC in writing of the direct or
indirect acquisition of control of the
foreign bank by any person or entity, or
group of persons or entities acting in
concert, within 14 calendar days after
the foreign bank becomes aware of a
change in control.
12 CFR 28.52 Covered under
Information Collection 1557–0081
(MA)—Reports of Condition and Income
(Interagency Call Report), FFIEC 031,
FFIEC 041 Allocated Transfer Risk
Reserve: A banking institution shall
establish an allocated transfer risk
reserve for specified international assets
when required by the OCC.
12 CFR 28.53 Accounting for Fees on
International Loans: Sets forth
restrictions on fees and specifies
accounting treatment for international
loans.
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12 CFR 28.54 Covered under
Information Collection 1557–0100
Country Exposure Report and Country
Exposure Information Report (FFIEC
009, FFIEC 009a) Reporting and
Disclosure of International Assets: A
banking institution shall submit to the
OCC, at least quarterly, information
regarding the amounts and composition
of its holdings of international assets. A
banking institution shall submit to the
OCC information regarding
concentrations in its holdings of
international assets that are material in
relation to total assets and to capital of
the institution.
Type of Review: Extension of a
currently approved collection.
Affected Public: Individuals;
Businesses or other for-profit.
Estimated Number of Respondents:
79.
Estimated Total Annual Responses:
117.
Frequency of Response: On occasion.
Estimated Total Annual Burden:
3,661.5.
All comments will become a matter of
public record. Comments are invited on:
(a) Whether the collection of
information is necessary for the proper
performance of the functions of the
agency, including whether the
information has practical utility;
(b) The accuracy of the agency’s
estimate of the burden of the collection
of information;
(c) Ways to enhance the quality,
utility, and clarity of the information to
be collected;
(d) Ways to minimize the burden of
the collection on respondents, including
through the use of automated collection
techniques or other forms of information
technology; and
(e) Estimates of capital or startup costs
and costs of operation, maintenance,
and purchase of services to provide
information.
Dated: June 8, 2006.
Stuart Feldstein,
Assistant Director, Legislative and Regulatory
Activities Division.
[FR Doc. E6–9229 Filed 6–13–06; 8:45 am]
BILLING CODE 4810–33–P
DEPARTMENT OF VETERANS
AFFAIRS
Joint Biomedical Laboratory Research
and Development and Clinical Science
Research and Development Services
Scientific Merit Review Board; Notice
of Meeting
The Department of Veterans Affairs
gives notice under the Public Law 92–
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Federal Register / Vol. 71, No. 114 / Wednesday, June 14, 2006 / Notices
rwilkins on PROD1PC63 with NOTICES
463 (Federal Advisory Committee Act)
that a subcommittee of the Joint
Biomedical Laboratory Research and
Development and Clinical Science
Research and Development Services
Scientific Merit Review Board will meet
from 8 a.m. to 5 p.m. on August 1, 2006
at the Doubletree Hotel, 1515 Rhode
Island Ave., NW., Washington, DC. The
subcommittee meeting will focus on
evaluating Pharmacogenomics Analysis
Laboratory proposals submitted by VA
investigators.
The purpose of the Merit Review
Board is to provide advice on the
scientific quality, budget, safety and
mission relevance of center-based
research proposals submitted for VA
merit review consideration. Proposals
submitted for review by the Board
involve a range of medical specialties
within the general areas of biomedical,
behavioral and clinical science research.
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The subcommittee meeting will be
open to the public for approximately
one hour at the start of its meeting to
discuss the general status of the
program. The remaining portion of the
meeting will be closed to the public for
the review, discussion, and evaluation
of initial and renewal projects.
The closed portion of the meeting
involves discussion, examination, and
reference to staff and consultant
critiques of research protocols. During
this portion of the subcommittee
meeting, discussion and
recommendations will deal with
qualifications of personnel conducting
the studies, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy, as well as
research information, the premature
disclosure of which could significantly
frustrate implementation of proposed
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34419
agency action regarding such research
projects.
As provided by subsection 10(d) of
Public Law 92–463, as amended, closing
portions of this meeting is in accordance
with 5 U.S.C., 552b(c)(6) and (9)(B).
Those who plan to attend or would like
to obtain a copy of minutes of the
subcommittee meeting and a roster of
the members of the subcommittee
should contact LeRoy G. Frey, PhD.,
Chief, Program Review (121F),
Department of Veterans Affairs, 810
Vermont Avenue, NW., Washington, DC
20420 at (202) 254–0288.
Dated: June 2, 2006.
By direction of the Secretary.
E. Philip Riggin,
Committee Management Officer.
[FR Doc. 06–5352 Filed 6–13–06; 8:45 am]
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Agencies
[Federal Register Volume 71, Number 114 (Wednesday, June 14, 2006)]
[Notices]
[Pages 34418-34419]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-5352]
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DEPARTMENT OF VETERANS AFFAIRS
Joint Biomedical Laboratory Research and Development and Clinical
Science Research and Development Services Scientific Merit Review
Board; Notice of Meeting
The Department of Veterans Affairs gives notice under the Public
Law 92-
[[Page 34419]]
463 (Federal Advisory Committee Act) that a subcommittee of the Joint
Biomedical Laboratory Research and Development and Clinical Science
Research and Development Services Scientific Merit Review Board will
meet from 8 a.m. to 5 p.m. on August 1, 2006 at the Doubletree Hotel,
1515 Rhode Island Ave., NW., Washington, DC. The subcommittee meeting
will focus on evaluating Pharmacogenomics Analysis Laboratory proposals
submitted by VA investigators.
The purpose of the Merit Review Board is to provide advice on the
scientific quality, budget, safety and mission relevance of center-
based research proposals submitted for VA merit review consideration.
Proposals submitted for review by the Board involve a range of medical
specialties within the general areas of biomedical, behavioral and
clinical science research.
The subcommittee meeting will be open to the public for
approximately one hour at the start of its meeting to discuss the
general status of the program. The remaining portion of the meeting
will be closed to the public for the review, discussion, and evaluation
of initial and renewal projects.
The closed portion of the meeting involves discussion, examination,
and reference to staff and consultant critiques of research protocols.
During this portion of the subcommittee meeting, discussion and
recommendations will deal with qualifications of personnel conducting
the studies, the disclosure of which would constitute a clearly
unwarranted invasion of personal privacy, as well as research
information, the premature disclosure of which could significantly
frustrate implementation of proposed agency action regarding such
research projects.
As provided by subsection 10(d) of Public Law 92-463, as amended,
closing portions of this meeting is in accordance with 5 U.S.C.,
552b(c)(6) and (9)(B). Those who plan to attend or would like to obtain
a copy of minutes of the subcommittee meeting and a roster of the
members of the subcommittee should contact LeRoy G. Frey, PhD., Chief,
Program Review (121F), Department of Veterans Affairs, 810 Vermont
Avenue, NW., Washington, DC 20420 at (202) 254-0288.
Dated: June 2, 2006.
By direction of the Secretary.
E. Philip Riggin,
Committee Management Officer.
[FR Doc. 06-5352 Filed 6-13-06; 8:45 am]
BILLING CODE 8320-01-M