Submission for OMB Review; Comment Request; National Evaluation of the Clinical and Translational Science Awards (CTSA) Initiative, 81611-81612 [2010-32659]
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Federal Register / Vol. 75, No. 248 / Tuesday, December 28, 2010 / Notices
1. Jan Malcolm Jones, Jr., and Leslie
Ann Jones, both in Jacksonville, Florida;
to retain outstanding voting shares of
Florida Capital Group, Inc., and thereby
indirectly retain outstanding voting
shares of Florida Capital Bank, both in
Jacksonville, Florida.
Board of Governors of the Federal
Reserve System, December 22, 2010.
Robert deV. Frierson,
Deputy Secretary of the Board.
Board of Governors of the Federal Reserve
System, December 22, 2010.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. 2010–32593 Filed 12–27–10; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Submission for OMB Review;
Comment Request; National
Evaluation of the Clinical and
Translational Science Awards (CTSA)
Initiative
[FR Doc. 2010–32651 Filed 12–27–10; 8:45 am]
BILLING CODE 6210–01–P
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies;
Correction
This notice corrects a notice (FR Doc.
2010–32092) published on page 80501
of the issue for Wednesday, December
22, 2010.
Under the Federal Reserve Bank of
New York heading, the entry for Chuo
Mitsui Trust Holding, Inc., Tokyo,
Japan, is revised to read as follows:
A. Federal Reserve Bank of New York
(Ivan Hurwitz, Vice President) 33
Liberty Street, New York, New York
10045–0001:
1. Chuo Mitsui Trust Holdings, Inc.,
Tokyo, Japan; to become a bank holding
Company by acquiring The Sumitomo
Trust and Banking Co., Ltd, Osaka,
Japan, and thereby acquire Sumitomo
Trust and Banking Co. (USA), Hoboken,
New Jersey.
In connection with this application,
Applicant also has applied to acquire
Nikko Americas Holding Co., Inc.,
Nikko Asset Management Americas,
Inc., and Chuo Mitsui Investments, all
in New York, New York, and thereby
engage in investment advisory activities,
pursuant to section 225.24(b)(6) of
Regulation Y.
Comments on this application must
be received by January 18, 2011.
Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Center for Research Resources, the
National Institutes of Health has
submitted to the Office of Management
and Budget (OMB) a request to review
and approve the information collection
listed below. This proposed information
collection was previously published in
the Federal Register on October 12,
2010, pages 62543–62544, and allowed
60-days for public comment. No
comments were received. The purpose
of this notice is to allow an additional
30 days for public comment. The
National Institutes of Health may not
conduct or sponsor, and the respondent
is not required to respond to, an
information collection that has been
extended, revised, or implemented on or
after October 1, 1995, unless it displays
a currently valid OMB control number.
Proposed Collection:
Title: The National Evaluation of the
Clinical and Translational Science
Awards (CTSA) Initiative.
Type of Information Collection
Request: New.
Need and Use of Information
Collection: The CTSA Initiative is
directed at transforming the way
biomedical research is conducted
nationwide by reducing the time it takes
SUMMARY:
Estimated
number of
respondents
Respondent type
for basic science or laboratory
discoveries to become treatments for
patients, and for those treatments in
turn to be incorporated and
disseminated throughout community
practice. The primary purpose of this
data collection is to provide information
about the process and early outcomes
associated with 46 awardees
participating in the first four cohorts of
CTSA awards, in order to fulfill the
congressional expectations for external
program evaluation. NIH will use the
results to understand the extent to
which the CTSA Initiative is bringing
about transformational changes in
clinical and translational science among
academic medical centers and their
research partners, increasing the
efficiency of the research process, and
enhancing the capacity of the field to
conduct clinical and translational
research. All information collected will
be used to provide analytical and policy
support to NCRR, assisting NIH in
making decisions about current CTSA
programming, future funding, and other
initiatives to improve clinical and
translational science. It may also
provide information for NIH’s
Government Performance and Results
Act (GPRA) report.
Frequency of Response: Biennial.
Affected Public: Individuals.
Type of Respondents: Scientific
researchers. The annual reporting
burden is as follows:
Estimated Number of Respondents:
3,563;
Estimated Number of Responses per
Respondent: 1;
Average Burden Hours Per Response:
0.13;
Estimated Total Annual Burden
Hours Requested: 451.5. The annualized
cost to respondents is estimated at
$14,056. There are no capital or start-up
costs, and no maintenance or service
cost components to report.
Estimated
number of
hours per
respondent
type
Frequency of
response
Estimated
total annual
burden hours
requested
emcdonald on DSK2BSOYB1PROD with NOTICES
Users survey ....................................................................................................
Nonusers survey ..............................................................................................
Trainees/scholars survey .................................................................................
Mentors survey ................................................................................................
500
500
1,213
1,350
.25
.08
.33
.25
.5
.5
.5
.5
62.5
20.0
200.0
169.0
Total ..........................................................................................................
........................
........................
........................
451.5
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies should
address one or more of the following
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22:37 Dec 27, 2010
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points: (1) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the function of the agency, including
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whether the information will have
practical utility; (2) Evaluate the
accuracy of the agency’s estimate of the
burden of the proposed collection of
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81612
Federal Register / Vol. 75, No. 248 / Tuesday, December 28, 2010 / Notices
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 the use
of appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs,
OIRA_submission@omb.eop.gov or by
fax to 202–395–6974, Attention: Desk
Officer for NIH. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and instruments, contact Patricia
Newman, Program Analyst, Office of
Science Policy, National Center for
Research Resources, 6701 Democracy
Boulevard, MSC 4874, Bethesda,
Maryland 20892–4874, or e-mail your
request, including your address to
pnewman@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30-days of the date of
this publication.
Dated: December 20, 2010.
Meryl Sufian,
Supervisory Health Science Policy Analyst,
Office of Science Policy, NCRR, National
Institutes of Health.
[FR Doc. 2010–32659 Filed 12–27–10; 8:45 am]
BILLING CODE 4140–01–P
FOR FURTHER INFORMATION CONTACT:
Karen Gorirossi or Sheila Fleming at
240–453–8800.
SUPPLEMENTARY INFORMATION:
I. Background
In FR Doc. 2010–29867 of November
29, 2010 (75 FR 73084–73085), there
was an error, which included an
incorrect date of implementation of
administrative actions. The error is
identified and corrected in the
Correction of Errors section below.
II. Correction of Errors
In FR Doc. 2010–29867 of November
29, 2010 (75 FR 73084–73085), make the
following corrections:
1. On page 73084, third column,
fourth paragraph, change the paragraph
to read as follows: ‘‘By letter dated
October 4, 2010, the Department of
Health and Human Services (HHS)
notified Dr. Sezen of findings of
misconduct in science made by ORI and
the Department’s intent to debar her for
a period of five (5) years pursuant to the
Public Health Service Policies on
Research Misconduct, 42 CFR part 50,
subpart A and part 93, and HHS’
Implementation (2 CFR part 376) of the
Office of Management and Budget
(OMB) Guidelines to Agencies on
Governmentwide Debarment and
Suspension (2 CFR part 180). In
accordance with part 93, subpart E, Dr.
Sezen was afforded 30 days within
which to request a hearing in this
matter. As of November 4, 2010, the
period of time to request a hearing
expired. Thus, the following
administrative actions have been
implemented for a period of five (5)
years, beginning on December 13, 2010.’’
Dated: December 17, 2010.
John Dahlberg,
Director, Division of Research Investigations,
Office of Research Integrity.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2010–32555 Filed 12–27–10; 8:45 am]
Office of the Secretary
BILLING CODE 4150–31–P
Findings of Misconduct in Science;
Correction
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary, HHS
ACTION: Correction of notice.
AGENCY:
[Docket No. HHS–OS–2010–0033; OCIIO–
9984–N]
This document corrects errors
that appeared in the notice published in
the November 29, Federal Register
entitled ‘‘Findings of Misconduct in
Science.’’
emcdonald on DSK2BSOYB1PROD with NOTICES
SUMMARY:
Effective Date: December 28,
2010.
Applicability Date: The correction
notice is applicable for the Findings of
Misconduct in Science notice published
on November 29, 2010.
DATES:
VerDate Mar<15>2010
23:49 Dec 27, 2010
Jkt 223001
The Consumer Operated and Oriented
Plan (CO–OP) Advisory Board; Office
of Consumer Information and
Insurance Oversight, January 13, 2011
Office of Consumer Information
and Insurance Oversight (OCIIO), HHS.
ACTION: Notice of meeting.
AGENCY:
This notice announces a
forthcoming meeting of an advisory
SUMMARY:
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Fmt 4703
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committee of the Office of Consumer
Information and Insurance Oversight
(OCIIO) in accordance with the Federal
Advisory Committee Act. The meeting
is open to the public. The purpose of the
meeting is to assist and advise the
Secretary and Congress through the
Department of Health and Human
Services’ Office of Consumer
Information and Insurance Oversight
(OCIIO) on the Department’s strategy to
foster the creation of qualified nonprofit
health insurance issuers. Specifically,
the Committee shall advise the
Secretary and Congress concerning the
award of grants and loans related to
Section 1322 of the Affordable Care Act.
In these matters, the Committee shall
consult with all components of the
Department, other federal entities, and
non-federal organizations, as
appropriate; and examine relevant data
sources to assess the grant and loan
award strategy to provide
recommendations to OCIIO. Notice of
this meeting is given under the Federal
Advisory Committee Act (Pub. L. No.
92–463, 5 U.S.C., App. 2).
DATES: Meeting Date: January 13, 2011
from 8 a.m. to 5 p.m., eastern standard
time (e.s.t.).
Deadline for Meeting Registration,
Presentations and Comments: January 6,
2011, 5 p.m., e.s.t.
Deadline for Requesting Special
Accommodations: January 6, 2011, 5
p.m., e.s.t.
ADDRESSES: Meeting Location: Jurys
Hotel, 1500 New Hampshire Ave., NW.,
Washington, DC 20036.
Meeting Online Access: To participate
in this meeting via the Internet, go to
https://www.readyshow.com/ and enter
participant code 78030350.
Meeting Phone Access: To participate
in this meeting via phone, please dial
into the toll free phone number 1–877–
366–0711, and enter the phone number
password 78030350#.
Meeting Registration, Presentations,
and Written Comments: Brian
Chiglinsky, Office of Consumer
Information and Insurance Oversight,
HHS, 200 Independence Avenue, SW.,
Washington, DC 20201, 202–260–6090,
Fax: 202–260–6108, or contact by e-mail
at brian.chiglinsky@hhs.gov.
Registration: The meeting is open to
the public, but attendance is limited to
the space available. Persons wishing to
attend this meeting must register by
contacting the Analyst at the address
listed in the ADDRESSES section of this
notice or by telephone at number listed
in the FOR FURTHER INFORMATION
CONTACT section of this notice, by the
date listed in the DATES section of this
notice.
E:\FR\FM\28DEN1.SGM
28DEN1
]]>Agencies
[Federal Register Volume 75, Number 248 (Tuesday, December 28, 2010)]
[Notices]
[Pages 81611-81612]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-32659]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Submission for OMB Review; Comment Request; National Evaluation
of the Clinical and Translational Science Awards (CTSA) Initiative
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National Center for Research Resources, the
National Institutes of Health has submitted to the Office of Management
and Budget (OMB) a request to review and approve the information
collection listed below. This proposed information collection was
previously published in the Federal Register on October 12, 2010, pages
62543-62544, and allowed 60-days for public comment. No comments were
received. The purpose of this notice is to allow an additional 30 days
for public comment. The National Institutes of Health may not conduct
or sponsor, and the respondent is not required to respond to, an
information collection that has been extended, revised, or implemented
on or after October 1, 1995, unless it displays a currently valid OMB
control number.
Proposed Collection:
Title: The National Evaluation of the Clinical and Translational
Science Awards (CTSA) Initiative.
Type of Information Collection Request: New.
Need and Use of Information Collection: The CTSA Initiative is
directed at transforming the way biomedical research is conducted
nationwide by reducing the time it takes for basic science or
laboratory discoveries to become treatments for patients, and for those
treatments in turn to be incorporated and disseminated throughout
community practice. The primary purpose of this data collection is to
provide information about the process and early outcomes associated
with 46 awardees participating in the first four cohorts of CTSA
awards, in order to fulfill the congressional expectations for external
program evaluation. NIH will use the results to understand the extent
to which the CTSA Initiative is bringing about transformational changes
in clinical and translational science among academic medical centers
and their research partners, increasing the efficiency of the research
process, and enhancing the capacity of the field to conduct clinical
and translational research. All information collected will be used to
provide analytical and policy support to NCRR, assisting NIH in making
decisions about current CTSA programming, future funding, and other
initiatives to improve clinical and translational science. It may also
provide information for NIH's Government Performance and Results Act
(GPRA) report.
Frequency of Response: Biennial.
Affected Public: Individuals.
Type of Respondents: Scientific researchers. The annual reporting
burden is as follows:
Estimated Number of Respondents: 3,563;
Estimated Number of Responses per Respondent: 1;
Average Burden Hours Per Response: 0.13;
Estimated Total Annual Burden Hours Requested: 451.5. The
annualized cost to respondents is estimated at $14,056. There are no
capital or start-up costs, and no maintenance or service cost
components to report.
----------------------------------------------------------------------------------------------------------------
Estimated
Estimated number of Estimated
Respondent type number of hours per Frequency of total annual
respondents respondent response burden hours
type requested
----------------------------------------------------------------------------------------------------------------
Users survey.................................... 500 .25 .5 62.5
Nonusers survey................................. 500 .08 .5 20.0
Trainees/scholars survey........................ 1,213 .33 .5 200.0
Mentors survey.................................. 1,350 .25 .5 169.0
---------------------------------------------------------------
Total....................................... .............. .............. .............. 451.5
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies should address one or more of the
following points: (1) Evaluate whether the proposed collection of
information is necessary for the proper performance of the function 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
[[Page 81612]]
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 the use of
appropriate automated, electronic, mechanical, or other technological
collection techniques or other forms of information technology.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974,
Attention: Desk Officer for NIH. To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact Patricia Newman, Program Analyst, Office of
Science Policy, National Center for Research Resources, 6701 Democracy
Boulevard, MSC 4874, Bethesda, Maryland 20892-4874, or e-mail your
request, including your address to pnewman@mail.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30-days
of the date of this publication.
Dated: December 20, 2010.
Meryl Sufian,
Supervisory Health Science Policy Analyst, Office of Science Policy,
NCRR, National Institutes of Health.
[FR Doc. 2010-32659 Filed 12-27-10; 8:45 am]
BILLING CODE 4140-01-P
