Proposed Data Collections Submitted for Public Comment and Recommendations, 492-493 [E7-25564]
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Federal Register / Vol. 73, No. 2 / Thursday, January 3, 2008 / Notices
FEDERAL RESERVE SYSTEM
Change in Bank Control Notices;
Acquisition of Shares of Bank or Bank
Holding Companies
The notificants listed below have
applied under the Change in Bank
Control Act (12 U.S.C. 1817(j)) and
§ 225.41 of the Board’s Regulation Y (12
CFR 225.41) to acquire a bank or bank
holding company. The factors that are
considered in acting on the notices are
set forth in paragraph 7 of the Act (12
U.S.C. 1817(j)(7)).
The notices are available for
immediate inspection at the Federal
Reserve Bank indicated. The notices
also will be available for inspection at
the office of the Board of Governors.
Interested persons may express their
views in writing to the Reserve Bank
indicated for that notice or to the offices
of the Board of Governors. Comments
must be received not later than January
18, 2008.
A. Federal Reserve Bank of San
Francisco (Tracy Basinger, Director,
Regional and Community Bank Group)
101 Market Street, San Francisco,
California 94105–1579:
1. Polamar QFP, LP, Long Beach,
California; to acquire 100 percent of the
voting shares of Palomar Enterprises,
LLC and thereby indirectly acquire
voting shares of Farmers & Merchants
Bank of Long Beach, both of Long
Beach, California.
Board of Governors of the Federal Reserve
System, December 28, 2007.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. E7–25562 Filed 1–2–08; 8:45 am]
inspection at the Federal Reserve Bank
indicated. The application also will 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.
Additional information on all bank
holding companies may be obtained
from the National Information Center
website at www.ffiec.gov/nic/.
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 January 28,
2008.
A. Federal Reserve Bank of
Minneapolis (Jacqueline G. King,
Community Affairs Officer) 90
Hennepin Avenue, Minneapolis,
Minnesota 55480–0291:
1. Frandsen Financial Corporation,
Arden Hills, Minnesota; to acquire 100
percent of the voting shares of The First
National Bank of Montgomery,
Montgomerey, Minnesota.
Board of Governors of the Federal Reserve
System, December 28, 2007.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. E7–25561 Filed 1–2–08; 8:45 am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
FEDERAL RESERVE SYSTEM
Centers for Disease Control and
Prevention
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
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BILLING CODE 6210–01–S
[60 Day–08–08AG]
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
VerDate Aug<31>2005
20:29 Jan 02, 2008
Jkt 214001
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 or send
comments to Maryam I. Daneshvar, CDC
Reports Clearance Officer, 1600 Clifton
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
Road, MS–D74, Atlanta, GA 30333 or
send an e-mail to omb@cdc.gov.
Comments are invited 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)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
HIV/AIDS Surveillance, Research, and
Intervention Methods and Materials
Development—New—National Center
for HIV, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Division of HIV/AIDS Prevention
(DHAP) within the National Center for
HIV, Hepatitis, STD, and TB Prevention
(NCHHSTP) of the Centers for Disease
Control and Prevention (CDC) is
planning to request the Office of
Management and Budget for a generic
clearance mechanism to support
behavioral projects. The projects
encompass several qualitative analytic
methods, intervention, and materials
development activities to be carried out
by CDC, its contractors, or its partners.
The major activities fall into six
categories based on their purpose and
intended use:
(1) Qualitative interviewing for HIV/
AIDS surveillance, research, and
intervention methods and material
development. Results of individual
interviews or group interviews are used
to develop population-appropriate
methods, interventions, and data
collection materials for current and
future projects.
(2) Cognitive interviewing for
development and testing of specific data
collection instruments used for HIV/
AIDS surveillance or research. Draft
instruments to be used by DHAP are
developed and tested through rounds of
cognitive interviews with volunteer
respondents. Results of cognitive
interviews are used to make instrument
design decisions that minimize response
error and reduce burden to the public.
(3) Research on methodology for HIV/
AIDS surveillance or research projects.
The purpose of the research is to
E:\FR\FM\03JAN1.SGM
03JAN1
493
Federal Register / Vol. 73, No. 2 / Thursday, January 3, 2008 / Notices
enhance understanding of the
psychology of participation and
response, to develop better standards for
project methodology and instrument
design, or to improve data collection
and other study procedures. Such
research could take the form of
experiments embedded within fielded
surveillance or research projects or
exploratory studies employing
individual interviews or focus groups.
(4) Research on utilizing computerassisted instruments (including webbased technology) for HIV surveillance
or research projects. This research uses
qualitative and quantitative data
collection methods with volunteer
respondents in order to assess the
design and use of computer-assisted
instruments.
(5) Pilot interviews. A limited number
of pilot interviews are conducted using
proposed instruments and data
respond to recruitment advertisements.
In addition to utilizing advertisements
for recruitment, respondents who will
participate in research on survey
methods may be selected purposively or
systematically from within an ongoing
surveillance or research project.
CDC estimates that an average of 1430
individuals will participate in HIV/
AIDS methods, intervention, and
instrument development activities in a
given year and the average annual
respondent burden is estimated to be
2135 hours. The estimates given below
cover the time that each respondent will
spend communicating with the
recruitment staff, in answering survey
questions and, in some cases, being
debriefed about the decision and recall
strategies they used. Participation of
respondents is voluntary and there is no
cost to the respondents other than their
time.
collection methodologies. Sources of
response error are identified through
examination of pilot data, observation
by methodologists, and techniques such
as the coding of the interviewerrespondent interaction. Respondents for
pilot interviews and interventions will
be selected using the methods
developed for the study that is being
piloted.
(6) Pilot testing of behavioral
interventions. Component testing will
assess acceptability and feasibility of
separate intervention activities. A
limited number of pilot tests are
conducted for behavioral interventions
prior to being tested in a ‘‘full
intervention trial.’’
Respondents who will participate in
individual and group interviews
(qualitative, cognitive, and computerassisted development activities) are
selected purposively from those who
ESTIMATE OF ANNUALIZED BURDEN TABLE
No. of respondents
Types of data collection
(1) Methods, interventions, and materials development—individual interviews ............................................................................................................
(2) Methods, interventions, and materials development—group interviews ...
(3) Research on survey methodology .............................................................
(4) Research on human-computer interface ....................................................
(5) Pilot interviewing ........................................................................................
(6) Pilot interventions .......................................................................................
Total ..........................................................................................................
Dated: December 26, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E7–25564 Filed 1–2–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Toxicology Program (NTP);
NTP Interagency Center for the
Evaluation of Alternative Toxicological
Methods (NICEATM); Workshop on
Acute Chemical Safety Testing:
Advancing In Vitro Approaches and
Humane Endpoints for Systemic
Toxicity Evaluations
National Institute of
Environmental Health Sciences
(NIEHS), National Institutes of Health
(NIH).
ACTION: Workshop announcement.
pwalker on PROD1PC71 with NOTICES
AGENCY:
The Interagency Committee
on the Validation of Alternative
SUMMARY:
VerDate Aug<31>2005
20:29 Jan 02, 2008
Jkt 214001
250
450
150
350
200
30
1,430
Methods (ICCVAM) and NICEATM
announce the upcoming ‘‘Scientific
Workshop on Acute Chemical Safety
Testing: Advancing In Vitro Approaches
and Humane Endpoints for Systemic
Toxicity Evaluations.’’ The goals of the
workshop are to:
(1) Review the state-of-the-science
and identify knowledge gaps regarding
the key pathways involved in acute
systemic toxicity.
(2) Recommend how these knowledge
gaps can be addressed by collecting
mechanistic biomarker data during
currently required in vivo safety testing.
(3) Recommend how key in vivo
pathway information can be used to
develop more predictive mechanismbased in vitro test systems and earlier,
more humane endpoints for in vivo test
methods.
(4) Recommend how mechanismbased in vitro test systems and earlier,
more humane endpoints can be used to
further reduce, refine, and eventually
replace animal use for acute systemic
toxicity testing while ensuring the
protection of human and animal health.
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
No. of responses per
respondent
Average burden per response
(in hours)
1
1
1
1
1
6
........................
1
2
1
1
1
2
........................
Total burden
(in hours)
250
900
150
350
200
360
2,210
This workshop is open to the public
with attendance limited only by the
space available.
DATES: The workshop will be held on
February 6–7, 2008.
ADDRESSES: The workshop will be held
at the NIH, Natcher Conference Center,
45 Center Drive, Bethesda, MD 20892. A
draft agenda and other information are
available on the ICCVAM workshop
Web site (https://iccvam.niehs.nih.gov/
meetings/AcuteToxWksp08/
AcuteToxWksp08.htm) and can be
obtained from NICEATM (see FOR
FURTHER INFORMATION CONTACT below).
FOR FURTHER INFORMATION CONTACT: Dr.
William S. Stokes, NICEATM Director,
NIEHS, P.O. Box 12233, MD EC–17,
Research Triangle Park, NC 27709,
(telephone) 919–541–2384, (fax) 919–
541–0947, (e-mail)
niceatm@niehs.nih.gov.
SUPPLEMENTARY INFORMATION:
Background
NICEATM and ICCVAM convened a
peer review panel meeting in 2006. The
panel was charged to determine the
E:\FR\FM\03JAN1.SGM
03JAN1
Agencies
[Federal Register Volume 73, Number 2 (Thursday, January 3, 2008)]
[Notices]
[Pages 492-493]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-25564]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-08-08AG]
Proposed Data Collections Submitted for Public Comment and
Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for opportunity for public comment on
proposed data collection projects, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To request more information on the proposed projects or to obtain a
copy of the data collection plans and instruments, call 404-639-5960 or
send comments to Maryam I. Daneshvar, CDC Reports Clearance Officer,
1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail to
omb@cdc.gov.
Comments are invited 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) ways to enhance the quality,
utility, and clarity of the information to be collected; and (d) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology. Written comments should be received
within 60 days of this notice.
Proposed Project
HIV/AIDS Surveillance, Research, and Intervention Methods and
Materials Development--New--National Center for HIV, STD, and TB
Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The Division of HIV/AIDS Prevention (DHAP) within the National
Center for HIV, Hepatitis, STD, and TB Prevention (NCHHSTP) of the
Centers for Disease Control and Prevention (CDC) is planning to request
the Office of Management and Budget for a generic clearance mechanism
to support behavioral projects. The projects encompass several
qualitative analytic methods, intervention, and materials development
activities to be carried out by CDC, its contractors, or its partners.
The major activities fall into six categories based on their
purpose and intended use:
(1) Qualitative interviewing for HIV/AIDS surveillance, research,
and intervention methods and material development. Results of
individual interviews or group interviews are used to develop
population-appropriate methods, interventions, and data collection
materials for current and future projects.
(2) Cognitive interviewing for development and testing of specific
data collection instruments used for HIV/AIDS surveillance or research.
Draft instruments to be used by DHAP are developed and tested through
rounds of cognitive interviews with volunteer respondents. Results of
cognitive interviews are used to make instrument design decisions that
minimize response error and reduce burden to the public.
(3) Research on methodology for HIV/AIDS surveillance or research
projects. The purpose of the research is to
[[Page 493]]
enhance understanding of the psychology of participation and response,
to develop better standards for project methodology and instrument
design, or to improve data collection and other study procedures. Such
research could take the form of experiments embedded within fielded
surveillance or research projects or exploratory studies employing
individual interviews or focus groups.
(4) Research on utilizing computer-assisted instruments (including
web-based technology) for HIV surveillance or research projects. This
research uses qualitative and quantitative data collection methods with
volunteer respondents in order to assess the design and use of
computer-assisted instruments.
(5) Pilot interviews. A limited number of pilot interviews are
conducted using proposed instruments and data collection methodologies.
Sources of response error are identified through examination of pilot
data, observation by methodologists, and techniques such as the coding
of the interviewer-respondent interaction. Respondents for pilot
interviews and interventions will be selected using the methods
developed for the study that is being piloted.
(6) Pilot testing of behavioral interventions. Component testing
will assess acceptability and feasibility of separate intervention
activities. A limited number of pilot tests are conducted for
behavioral interventions prior to being tested in a ``full intervention
trial.''
Respondents who will participate in individual and group interviews
(qualitative, cognitive, and computer-assisted development activities)
are selected purposively from those who respond to recruitment
advertisements. In addition to utilizing advertisements for
recruitment, respondents who will participate in research on survey
methods may be selected purposively or systematically from within an
ongoing surveillance or research project.
CDC estimates that an average of 1430 individuals will participate
in HIV/AIDS methods, intervention, and instrument development
activities in a given year and the average annual respondent burden is
estimated to be 2135 hours. The estimates given below cover the time
that each respondent will spend communicating with the recruitment
staff, in answering survey questions and, in some cases, being
debriefed about the decision and recall strategies they used.
Participation of respondents is voluntary and there is no cost to the
respondents other than their time.
Estimate of Annualized Burden Table
----------------------------------------------------------------------------------------------------------------
No. of Average burden
Types of data collection No. of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
(1) Methods, interventions, and materials 250 1 1 250
development--individual interviews.............
(2) Methods, interventions, and materials 450 1 2 900
development--group interviews..................
(3) Research on survey methodology.............. 150 1 1 150
(4) Research on human-computer interface........ 350 1 1 350
(5) Pilot interviewing.......................... 200 1 1 200
(6) Pilot interventions......................... 30 6 2 360
Total....................................... 1,430 .............. .............. 2,210
----------------------------------------------------------------------------------------------------------------
Dated: December 26, 2007.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E7-25564 Filed 1-2-08; 8:45 am]
BILLING CODE 4163-18-P