Agency Information Collection Request; 60-Day Public Comment Request, 23249-23250 [2012-9323]
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23249
Federal Register / Vol. 77, No. 75 / Wednesday, April 18, 2012 / Notices
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than May 13, 2012.
A. Federal Reserve Bank of San
Francisco (Kenneth Binning, Vice
President, Applications and
Enforcement) 101 Market Street, San
Francisco, California 94105–1579:
1. Mitsubishi UFJ Financial Group,
Inc., The Bank of Tokyo-Mitsubishi UFJ,
Ltd, both in Tokyo, Japan, and
UnionBanCal Corporation, San
Francisco, California; to acquire 100
percent of the voting shares of Pacific
Capital Bancorp and thereby indirectly
acquire Santa Barbara Bank & Trust,
both of Santa Barbara, California.
In connection with this application,
UnionBanCal Corporation has applied
to merge with and into Pacific Capital
Bancorp.
Board of Governors of the Federal Reserve
System, April 13, 2012.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. 2012–9321 Filed 4–17–12; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier OS–0990–0279]
Agency Information Collection
Request; 60-Day Public Comment
Request
Office of the Secretary, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Office of the Secretary (OS), Department
of Health and Human Services, is
publishing the following summary of a
proposed information collection request
for public comment. Interested persons
are invited to send comments regarding
this burden estimate or any other aspect
of this collection of information,
including any of the following subjects:
(1) The necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions; (2) the accuracy of the
estimated burden; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4) the
use of automated collection techniques
or other forms of information
AGENCY:
technology to minimize the information
collection burden.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, email your request,
including your address, phone number,
OMB number, and OS document
identifier, to
Sherette.funncoleman@hhs.gov, or call
the Reports Clearance Office on (202)
690–5683. Written comments and
recommendations for the proposed
information collections must be directed
to the OS Paperwork Clearance Officer
at the above email within 60 days.
Proposed Project: Institutional Review
Board Form—Extension—OMB No.
0990–0279—Office for Human Research
Protections.
Abstract: The Office for Human
Research Protections (OHRP) and the
Food and Drug Administration (FDA)
are requesting a three-year extension of
the OMB No. 0990–0279, Institutional
Review Board (IRB) Registration Form.
This form was modified in 2009 to be
consistent with IRB registration
requirements that were adopted in July
2009 by OHRP and FDA, respectively.
Respondents for this information
collection are institutions or
organizations operating IRBs designated
by an institution under an assurance of
compliance approved for federalwide
use by OHRP under 45 CFR 46.103(a)
and that review human subjects
research conducted or supported by
HHS, or, in the case of FDA’s regulation,
each IRB in the United States that
reviews clinical investigations regulated
by FDA under sections 505(i) or 520(g)
of the Federal Food, Drug and Cosmetic
Act; and each IRB in the United States
that reviews clinical investigations that
are intended to support applications for
research or marketing permits for FDAregulated products.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
6,100
900
2
2
1
1
12,200
1,800
Total ..........................................................................................................
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IRB Registration—0279 ...................................................................................
........................
........................
........................
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18APN1
23250
Federal Register / Vol. 77, No. 75 / Wednesday, April 18, 2012 / Notices
Keith A. Tucker,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
[FR Doc. 2012–9323 Filed 4–17–12; 8:45 am]
BILLING CODE 4150–36–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
HIT Standards Committee; Schedule
for the Assessment of HIT Policy
Committee Recommendations
Office of the National
Coordinator for Health Information
Technology, HHS.
ACTION: Notice.
AGENCY:
Section 3003(b)(3) of the
American Recovery and Reinvestment
Act of 2009 mandates that the HIT
Standards Committee develop a
schedule for the assessment of policy
recommendations developed by the HIT
Policy Committee and publish it in the
Federal Register. This notice fulfills the
requirements of Section 3003(b)(3) and
updates the schedule posted in the
Federal Register on May 4, 2011. In
anticipation of receiving
recommendations originally developed
by the HIT Policy Committee, the HIT
Standards Committee has created four
(4) workgroups to analyze the areas of
clinical quality, clinical operations,
implementation, and privacy and
security. Other groups are convened to
address specific issues as needed, such
as the Nationwide Health Information
Network Power Team, the Consumer/
Patient Engagement Power Team, and
the Vocabulary Task Force.
HIT Standards Committee’s Schedule
for the Assessment of HIT Policy
Committee Recommendations is as
follows:
The National Coordinator will
establish priority areas based in part on
recommendations received from the HIT
Policy Committee regarding health
information technology standards,
implementation specifications, and/or
certification criteria. Once the HIT
Standards Committee is informed of
those priority areas, it will:
(A) Direct the appropriate workgroup
or other special group to develop a
report for the HIT Standards Committee,
to the extent possible, within 90 days,
which will include, among other items,
the following:
(1) An assessment of what standards,
implementation specifications, and
certification criteria are currently
available to meet the priority area;
(2) an assessment of where gaps exist
(i.e., no standard is available or
harmonization is required because more
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than one standard exists) and identify
potential organizations that have the
capability to address those gaps; and
(3) a timeline, which may also
account for NIST testing, where
appropriate, and include dates when the
HIT Standards Committee is expected to
issue recommendation(s) to the National
Coordinator.
(B) Upon receipt of a report from a
workgroup or other special group, the
HIT Standards Committee will:
(1) Accept the timeline provided by
the subcommittee, and, if necessary,
revise it; and
(2) Assign subcommittee(s) to conduct
research and solicit testimony, where
appropriate, and issue
recommendations to the full committee
in a timely manner.
(C) Advise the National Coordinator,
consistent with the accepted timeline in
(B)(1) and after NIST testing, where
appropriate, on standards,
implementation specifications, and/or
certification criteria, for the National
Coordinator’s review and determination
whether or not to endorse the
recommendations, and possible
adoption of the proposed
recommendations by the Secretary of
the Department of Health and Human
Services.
The standards and related topics
which the HIT Standards Committee is
expected to address over the coming
year include, but may not be limited to:
Quality measurement; the extended
portfolio of standards for the nationwide
health information network; distributed
queries and results; radiology;
consumer-mediated information
exchange; public health; data
portability; and a process for the
maintenance of standards.
For a listing of upcoming HIT
Standards Committee meetings, please
visit the ONC web site at https://
healthit.hhs.gov.
Notice of this schedule is given under
the American Recovery and
Reinvestment Act of 2009 (Pub. L. 111–
5), section 3003.
Dated: April 11, 2012.
MacKenzie Robertson,
FACA Program Manager, Office of Policy and
Planning, Office of the National Coordinator
for Health Information Technology.
[FR Doc. 2012–9251 Filed 4–17–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Statement of Organization, Functions,
and Delegations of Authority;
Administration for Community Living
Department of Health and
Human Services.
AGENCY:
ACTION:
Notice.
The Department of Health and
Human Services establishes the
Administration for Community Living
in order to achieve several important
objectives: reduce the fragmentation that
currently exists in Federal programs
addressing the community living service
and support needs of both the aging and
disability populations; enhance access
to quality health care and long-term
services and supports for all
individuals; promote consistency in
community living policy across other
areas of the Federal government; and
complement the community
infrastructure, as supported by both
Medicaid and other Federal programs,
in order to better respond to the full
spectrum of needs of seniors and
persons with disabilities.
SUMMARY:
Dan
Berger, Administration for Community
Living, 1 Massachusetts Avenue NW.,
Washington, DC 20201, 202–357–3419
FOR FURTHER INFORMATION CONTACT:
This
notice amends Part B of the Statement
of Organization, Functions, and
Delegations of Authority of the
Department of Health and Human
Services (HHS), Administration on
Aging, as last amended at 75 FR 18219–
18228, dated April 9, 2010, and 76 FR
5178, dated January 28, 2011; Part K of
the Statement of Organization,
Functions, and Delegations of Authority
of the Department of Health and Human
Services, Administration for Children
and Families, at Chapter K,
Administration on Children and
Families, as last amended at 75 FR
60471–60473, dated September 30,
2010, and at Chapter KC,
Administration on Developmental
Disabilities, as last amended at 76 FR
72418–72420, dated November 23, 2011;
Part A of the Statement of Organization,
Functions, and Delegations of Authority
of the Department of Health and Human
Services, Office of the Secretary,
Immediate Office of the Secretary, at
Chapter AA, Immediate Office of the
Secretary, as last amended at 76 FR
42710–11, dated July 19, 2011, and at
Chapter AAC, Office on Disability, as
last amended at 67 FR 70433, dated
November 22, 2002; as follows:
SUPPLEMENTARY INFORMATION:
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]]>Agencies
[Federal Register Volume 77, Number 75 (Wednesday, April 18, 2012)]
[Notices]
[Pages 23249-23250]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-9323]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier OS-0990-0279]
Agency Information Collection Request; 60-Day Public Comment
Request
AGENCY: Office of the Secretary, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Office of the Secretary (OS),
Department of Health and Human Services, is publishing the following
summary of a proposed information collection request for public
comment. Interested persons are invited to send comments regarding this
burden estimate or any other aspect of this collection of information,
including any of the following subjects: (1) The necessity and utility
of the proposed information collection for the proper performance of
the agency's functions; (2) the accuracy of the estimated burden; (3)
ways to enhance the quality, utility, and clarity of the information to
be collected; and (4) the use of automated collection techniques or
other forms of information technology to minimize the information
collection burden.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, email your
request, including your address, phone number, OMB number, and OS
document identifier, to Sherette.funncoleman@hhs.gov, or call the
Reports Clearance Office on (202) 690-5683. Written comments and
recommendations for the proposed information collections must be
directed to the OS Paperwork Clearance Officer at the above email
within 60 days.
Proposed Project: Institutional Review Board Form--Extension--OMB
No. 0990-0279--Office for Human Research Protections.
Abstract: The Office for Human Research Protections (OHRP) and the
Food and Drug Administration (FDA) are requesting a three-year
extension of the OMB No. 0990-0279, Institutional Review Board (IRB)
Registration Form. This form was modified in 2009 to be consistent with
IRB registration requirements that were adopted in July 2009 by OHRP
and FDA, respectively. Respondents for this information collection are
institutions or organizations operating IRBs designated by an
institution under an assurance of compliance approved for federalwide
use by OHRP under 45 CFR 46.103(a) and that review human subjects
research conducted or supported by HHS, or, in the case of FDA's
regulation, each IRB in the United States that reviews clinical
investigations regulated by FDA under sections 505(i) or 520(g) of the
Federal Food, Drug and Cosmetic Act; and each IRB in the United States
that reviews clinical investigations that are intended to support
applications for research or marketing permits for FDA-regulated
products.
Total Estimated Annualized Burden--Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Form name respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
IRB Registration--0279.......................... 6,100 2 1 12,200
900 2 1 1,800
---------------------------------------------------------------
Total....................................... .............. .............. .............. 14,000
----------------------------------------------------------------------------------------------------------------
[[Page 23250]]
Keith A. Tucker,
Paperwork Reduction Act Reports Clearance Officer, Office of the
Secretary.
[FR Doc. 2012-9323 Filed 4-17-12; 8:45 am]
BILLING CODE 4150-36-P
