Proposed Data Collections Submitted for Public Comment and Recommendations, 33823-33824 [E8-13317]
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Federal Register / Vol. 73, No. 115 / Friday, June 13, 2008 / Notices
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 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 July 10, 2008.
A. Federal Reserve Bank of
Philadelphia (Michael E. Collins, Senior
Vice President) 100 North 6th Street,
Philadelphia, Pennsylvania 19105–
1521:
1. Nova Financial Holdings, Inc.,
Berwyn, Pennsylvania, to acquire 100
percent of the voting shares of
Pennsylvania Business Bank,
Philadelphia, Pennsylvania.
Board of Governors of the Federal Reserve
System, June 10, 2008.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. E8–13333 Filed 6–12–08; 8:45 am]
BILLING CODE 6210–01–S
FEDERAL RESERVE SYSTEM
rwilkins on PROD1PC63 with NOTICES
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies;
Correction
This notice corrects a notice (FR Doc.
E8-12885 published on page 32709 of
the issue for Tuesday, June 10, 2008.
Under the Federal Reserve Bank of
Kansas City heading, the entry for
Pinnacle Bancorp, Inc., Central City,
Nebraska, is revised to read as follows:
A. Federal Reserve Bank of Kansas
City (Todd Offenbacker, Assistant Vice
President) 1 Memorial Drive, Kansas
City, Missouri 64198–0001:
VerDate Aug<31>2005
17:34 Jun 12, 2008
Jkt 214001
1. Pinnacle Bancorp, Inc., Central
City, Nebraska, to acquire 100 percent of
the voting shares of First Azle
Bancshares, Inc., Azle, Texas, and
thereby indirectly acquire voting shares
of Wood Financial Group, Inc., Dover,
Delaware, and First Bank, Azle, Texas.
Comments on this application must
be received by July 3, 2008.
Board of Governors of the Federal Reserve
System, June 10, 2008.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. E8–13334 Filed 6–12–08 8:45 am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–08–08BF]
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 and
send comments to Maryam I. Daneshvar,
CDC Acting 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
Evaluation Models to Assess Patient
Perspectives on Opt-out HIV testing in
Clinical Settings—New—National
PO 00000
Frm 00023
Fmt 4703
Sfmt 4703
33823
Center for HIV, Viral Hepatitis, STD and
TB Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 2006, CDC published the Revised
Recommendations for HIV Testing of
Adults, Adolescents and Pregnant
Women in Health Care Settings which
recommends routine, opt-out HIV
testing to persons 13–64 years of age in
health care settings. The goal of this
project is to develop evaluation models
for health care providers in a variety of
settings to independently assess the
effect that expanded HIV screening
activities have on patient attitudes
toward and acceptance of HIV testing.
The evaluation models will be
packaged into a toolkit containing
educational materials, administrative
tools and a model questionnaire to
measure patients’ perceptions of their
ability to decline testing, the sufficiency
and effectiveness of methods used to
impart information prior to testing, and
satisfaction with the testing process.
As part of the development of a model
questionnaire for inclusion in the
toolkit, three health care settings (a
hospital emergency department, a
private primary care practice and a
public primary care practice) will be
selected to pilot test the questionnaire.
In each health care site, 150 patients
will be asked to voluntarily complete a
brief computer assisted self interview
regarding their experience with the HIV
testing process during their health care
visit.
Collection of data will include
information on patient demographics
and current behaviors that may facilitate
HIV transmission; perceptions regarding
pressure to take the test; confidentiality
and privacy during testing; and patient
satisfaction and acceptance of opt-out
HIV testing. For persons who refused
HIV testing during their visit,
information about refusal will be
collected.
Results from the three pilot sites will
be assessed to understand issues of
feasibility of the model questionnaire
and validity of the included items and
scales. The findings from the three site
evaluations will be used to improve the
model questionnaire and protocols
included in the evaluation models
toolkit.
CDC plans to complete data collection
in 3 health care settings in one year.
CDC estimates that 188 patients will be
asked to participate at each site during
the one year of data collection and that
80% will accept, resulting in
approximately 450 new survey
respondents across all sites. The average
E:\FR\FM\13JNN1.SGM
13JNN1
33824
Federal Register / Vol. 73, No. 115 / Friday, June 13, 2008 / Notices
duration of the survey is estimated to be
20 minutes.
Participation is voluntary. There is no
cost to the respondents other than their
time.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of data collection
Number of
respondents
Average
number of
responses per
respondent
Average
burden per
response
(hours)
Total burden
(hours)
Clinic Patient Survey .......................................................................................
450
1
20/60
150
Dated: June 9, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–13317 Filed 6–12–08; 8:45 am]
BILLING CODE 4163–18–P
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Disease Control and
Prevention
rwilkins on PROD1PC63 with NOTICES
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the Board
of Scientific Counselors, National
Center for Environmental Health/
Agency for Toxic Substances and
Disease Registry, Department of Health
and Human Services, has been renewed
for a 2-year period through May 21,
2010.
For information, contact Mark Bashor,
Ph.D., Executive Secretary, Board of
Scientific Counselors, National Center
for Environmental Health/Agency for
Toxic Substances and Disease Registry,
Department of Health and Human
Services, 4770 Buford Highway,
Mailstop F61, Chamblee, Georgia 30341,
telephone 770/488–0574 or fax 770/
488–3377.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: June 6, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E8–13318 Filed 6–12–08; 8:45 am]
BILLING CODE 4163–18–P
Jkt 214001
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
and Human Services, is publishing the
following summary of proposed
collections 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 function;
(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.
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: The Fiscal
Soundness Reporting Requirements;
Use: CMS is assigned responsibility for
overseeing all Medicare Advantage
Organizations (MAO) on-going financial
performance. CMS needs the requested
collection of information to establish
that each MAO maintains a fiscally
sound organization. Form Number:
CMS–906 (OMB# 0938–0469);
Frequency: Yearly; Affected Public:
Business or other for-profits and not-forprofit institutions; Number of
Respondents: 700; Total Annual
AGENCY:
Board of Scientific Counselors,
National Center for Environmental
Health/Agency for Toxic Substances
and Disease Registry: Notice of
Charter Renewal
16:18 Jun 12, 2008
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–906, CMS–1696,
and CMS–10167]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
VerDate Aug<31>2005
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
PO 00000
Frm 00024
Fmt 4703
Sfmt 4703
Responses: 700; Total Annual Hours:
233.
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Appointment of
Representative; Use: This form will be
completed by beneficiaries, providers
and suppliers who wish to appoint
representatives to assist them with
obtaining initial determinations and
filing appeals. The appointment of
representative form must be signed by
the party making the appointment and
the individual agreeing to accept the
appointment. Form Number: CMS–1696
(OMB# 0938–0950); Frequency:
Occasionally; Affected Public:
Individuals or households and business
or other for-profits; Number of
Respondents: 268,268; Total Annual
Responses: 268,268; Total Annual
Hours: 67,067.
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Competitive
Acquisition Program for Medicare Part B
Drugs: CAP Physician Election
Agreement; Use: The Competitive
Acquisition Program (CAP) is required
by Section 303(d) of the Medicare
Modernization Act (MMA), which
amended Title XVIII of the Social
Security Act (the Act) by adding a new
section 1847(B), which establishes a
competitive acquisition program for the
payment for Part B covered drugs and
biologicals furnished on or after January
1, 2006. Physicians are given a choice
between buying and billing these drugs
under the average sales price (ASP)
system, or obtaining these drugs from
vendors selected in a competitive
bidding process. Section 108 of the
Medicare Improvements and Extension
Act under Division B, Title I of the Tax
Relief Health Care Act of 2006 amended
Section 1847(b)(a)(3) of the Act and
requires that CAP implement a post
payment review process.
The CAP Physician Election
Agreement is used annually by
physicians to elect to participate in the
CAP or to make changes to the previous
E:\FR\FM\13JNN1.SGM
13JNN1
Agencies
[Federal Register Volume 73, Number 115 (Friday, June 13, 2008)]
[Notices]
[Pages 33823-33824]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-13317]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-08-08BF]
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
and send comments to Maryam I. Daneshvar, CDC Acting 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
Evaluation Models to Assess Patient Perspectives on Opt-out HIV
testing in Clinical Settings--New--National Center for HIV, Viral
Hepatitis, STD and TB Prevention (NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
In 2006, CDC published the Revised Recommendations for HIV Testing
of Adults, Adolescents and Pregnant Women in Health Care Settings which
recommends routine, opt-out HIV testing to persons 13-64 years of age
in health care settings. The goal of this project is to develop
evaluation models for health care providers in a variety of settings to
independently assess the effect that expanded HIV screening activities
have on patient attitudes toward and acceptance of HIV testing.
The evaluation models will be packaged into a toolkit containing
educational materials, administrative tools and a model questionnaire
to measure patients' perceptions of their ability to decline testing,
the sufficiency and effectiveness of methods used to impart information
prior to testing, and satisfaction with the testing process.
As part of the development of a model questionnaire for inclusion
in the toolkit, three health care settings (a hospital emergency
department, a private primary care practice and a public primary care
practice) will be selected to pilot test the questionnaire. In each
health care site, 150 patients will be asked to voluntarily complete a
brief computer assisted self interview regarding their experience with
the HIV testing process during their health care visit.
Collection of data will include information on patient demographics
and current behaviors that may facilitate HIV transmission; perceptions
regarding pressure to take the test; confidentiality and privacy during
testing; and patient satisfaction and acceptance of opt-out HIV
testing. For persons who refused HIV testing during their visit,
information about refusal will be collected.
Results from the three pilot sites will be assessed to understand
issues of feasibility of the model questionnaire and validity of the
included items and scales. The findings from the three site evaluations
will be used to improve the model questionnaire and protocols included
in the evaluation models toolkit.
CDC plans to complete data collection in 3 health care settings in
one year. CDC estimates that 188 patients will be asked to participate
at each site during the one year of data collection and that 80% will
accept, resulting in approximately 450 new survey respondents across
all sites. The average
[[Page 33824]]
duration of the survey is estimated to be 20 minutes.
Participation is voluntary. There is no cost to the respondents
other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average number Average burden
Type of data collection Number of of responses per response Total burden
respondents per respondent (hours) (hours)
----------------------------------------------------------------------------------------------------------------
Clinic Patient Survey....................... 450 1 20/60 150
----------------------------------------------------------------------------------------------------------------
Dated: June 9, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-13317 Filed 6-12-08; 8:45 am]
BILLING CODE 4163-18-P