Proposed Data Collections Submitted for Public Comment and Recommendations, 35391-35392 [E8-14152]
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Federal Register / Vol. 73, No. 121 / Monday, June 23, 2008 / Notices
Federal Communications Commission.
Marlene H. Dortch,
Secretary.
[FR Doc. E8–14133 Filed 6–20–08; 8:45 am]
BILLING CODE 6712–01–P
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Change in Bank Control Notices;
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The notificants listed below have
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§ 225.41 of the Board’s Regulation Y (12
CFR 225.41) to acquire a bank or bank
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U.S.C. 1817(j)(7)).
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views in writing to the Reserve Bank
indicated for that notice or to the offices
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must be received not later than July 8,
2008.
A. Federal Reserve Bank of Atlanta
(Steve Foley, Vice President) 1000
Peachtree Street, N.E., Atlanta, Georgia
30309:
1. William E. Arnold, John M.
Hubbard, Kellee S. Whitehurst, Betty W.
Arnold, and William E. Arnold, as
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Florida.
Board of Governors of the Federal Reserve
System, June 18, 2008.
Margaret McCloskey Shanks,
Associate Secretary of the Board.
[FR Doc. E8–14085 Filed 6–20–08; 8:45 am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the Secretary’s Advisory
Committee on Human Research
Protections
Department of Health and
Human Services, Office of the Secretary,
Office of Public Health and Science.
ACTION: Notice.
mmaher on PROD1PC70 with NOTICES
AGENCY:
SUMMARY: Pursuant to Section 10(a) of
the Federal Advisory Committee Act,
VerDate Aug<31>2005
01:51 Jun 21, 2008
Jkt 214001
U.S.C. Appendix 2, notice is hereby
given that the Secretary’s Advisory
Committee on Human Research
Protections (SACHRP) will hold its
sixteenth meeting. The meeting will be
open to the public.
DATES: The meeting will be held on
Tuesday, July 15, 2008, from 8:30 a.m.
until 4:30 p.m. and Wednesday, July 16,
2008, from 8:30 a.m. until 4:30 p.m.
ADDRESSES: The Sheraton National
Hotel, 900 South Orme Street,
Arlington, Virginia 22204. Phone: 703–
521–1900.
FOR FURTHER INFORMATION CONTACT: Ivor
Pritchard, PhD, Acting Director, Office
for Human Research Protections, or Julia
Gorey, J.D., Acting Executive Director,
SACHRP; U.S. Department of Health
and Human Services, 1101 Wootton
Parkway, Suite 200, Rockville,
Maryland 20852; 240–453–6900; fax:
240–453–6909; E-mail address:
sachrp@osophs.dhhs.gov.
SUPPLEMENTARY INFORMATION: Under the
authority of 42 U.S.C. 217a, Section 222
of the Public Health Service Act, as
amended, SACHRP was established to
provide expert advice and
recommendations to the Secretary of
Health and Human Services and the
Assistant Secretary for Health on issues
and topics pertaining to or associated
with the protection of human research
subjects.
On July 15, 2008, SACHRP will
receive and discuss a report from the
Subcommittee on Inclusion of
Individuals with Impaired DecisionMaking in Research. The Subcommittee
on Inclusion of Individuals with
Impaired Decision-Making in Research
is charged with developing
recommendations for consideration by
SACHRP about whether guidance and/
or additional regulations are needed for
research involving individuals with
impaired decision-making capacity.
This subcommittee was formed as a
result of discussions during the July 31–
August 1, 2006 SACHRP meeting. In
addition, an invited panel will discuss
ethical issues associated with tissue
repositories and biological specimens,
including questions surrounding
community consent, appropriateness
and validity of consent for unspecified
uses, and appropriate waiver of consent.
On July 16, 2008, the Committee will
receive and discuss a report from the
Subpart A Subcommittee. The Subpart
A Subcommittee is charged with
developing recommendations for
consideration by SACHRP about the
application of Subpart A of 45 CFR part
46 in the current research environment.
This subcommittee was established by
SACHRP at its October 4–5, 2006
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35391
meeting. In addition, SACHRP members
will make brief presentations on the
problems and issues they see with the
present Human Subjects Protection
System, followed by a period of
discussion.
Public attendance at the meeting is
limited to space available. Individuals
who plan to attend the meeting and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the designated contact persons.
Members of the public will have the
opportunity to provide comments on
both days of the meeting. Public
comment will be limited to five minutes
per speaker. Any members of the public
who wish to have printed materials
distributed to SACHRP members for this
scheduled meeting should submit
materials to the Acting Executive
Director, SACHRP, prior to the close of
business Monday, June 30, 2008.
Information about SACHRP and the
draft meeting agenda will be posted on
the SACHRP Web site at: https://
www.hhs.gov/ohrp/sachrp/.
Dated: June 16, 2008.
Ivor A. Pritchard,
Acting Director, Office for Human Research
ProtectionsActing Executive Secretary,
Secretary’s Advisory Committee on Human
Research Protections.
[FR Doc. E8–14035 Filed 6–20–08; 8:45 am]
BILLING CODE 4150–36–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–08–0706]
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
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
E:\FR\FM\23JNN1.SGM
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35392
Federal Register / Vol. 73, No. 121 / Monday, June 23, 2008 / Notices
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
National Program of Cancer Registries
Program Evaluation Instrument (NPCR–
PEI)—Revision—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC is responsible for administering
and monitoring the National Program of
Cancer Registries (NPCR). The NPCR
provides technical assistance and
funding and sets program standards to
assure that complete local, state,
regional, and national cancer incidence
data are available for national and state
cancer control and prevention activities
and health planning activities. As of
2008, CDC supports 49 populationbased central cancer registries (CCR) in
(12) survey feedback. Examples of
information that can be obtained from
various questions include, but are not
limited to: (1) Number of filled full-time
staff positions by position
responsibility; (2) legislation protecting
the confidentiality of CCR data; (3) data
quality control activities; (4) data
collection activities as they relate to
achieving NPCR standards for data
completeness; and (5) whether or not
registry data are used for comprehensive
cancer control programs, needs
assessment/program planning, clinical
studies, or incidence and mortality
estimates.
The NPCR–PEI is needed in order to
receive, process, evaluate, aggregate,
and disseminate NPCR program
information. The information is used by
CDC and the NPCR-funded registries to
monitor progress toward meeting
established program standards, goals,
and objectives; to evaluate various
attributes of the registries funded by
NPCR; and to respond to data inquiries
made by CDC and other agencies of the
federal government.
CDC requests OMB approval for a
period of three years to collect
information in the summer of 2009 and
the summer of 2011. There are no costs
to respondents except their time.
The estimated annualized burden
hours are summarized in the table
below.
45 states, two territories, the District of
Columbia, and the Pacific Islands. The
National Cancer Institute supports the
operations of CCRs in the five remaining
states.
Cancer registries currently submit
information about registry operations to
CDC on an annual basis via a secure,
web-based Annual Program Evaluation
Instrument (APEI) (OMB 0920–0706,
exp. 12/31/2008). During the next OMB
approval period, CDC proposes to
change the data collection frequency
from annual to every other year, with
data collection occurring only in oddnumbered years. This change will
reduce burden to respondents. The
project title and the instrument will be
revised to reflect the change in data
collection frequency (from National
Program of Cancer Registries Annual
Program Evaluation Instrument (NPCR–
APEI) to National Program of Cancer
Registries Program Evaluation
Instrument (NPCR–PEI)).
The Program Evaluation Instrument
(NCPR–PEI) includes questions about
the following categories of registry
operations: (1) Staffing, (2) legislation,
(3) administration, (4) reporting
completeness, (5) data exchange, (6)
data content and format, (7) data quality
assurance, (8) data use, (9) collaborative
relationships, (10) advanced activities,
(11) ‘‘success stories’’ that summarize
ways in which CCR data are used, and
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
NPCR Grantees ...............................................................................................
Dated: June 13, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–14152 Filed 6–20–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
mmaher on PROD1PC70 with NOTICES
[60Day–08–08BE]
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
VerDate Aug<31>2005
01:51 Jun 21, 2008
Jkt 214001
33
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)
PO 00000
Frm 00027
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
(in hours)
1
Total burden
(in hours)
1.5
50
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
Chronic Hepatitis Cohort Study
(CHeCS)—New—National Center for
HIV, Hepatitis, STD, and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Approximately 3.2 million Americans
are chronically infected with hepatitis C
virus and 1.25 million Americans are
E:\FR\FM\23JNN1.SGM
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]]>Agencies
[Federal Register Volume 73, Number 121 (Monday, June 23, 2008)]
[Notices]
[Pages 35391-35392]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-14152]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-08-0706]
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 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
[[Page 35392]]
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
National Program of Cancer Registries Program Evaluation Instrument
(NPCR-PEI)--Revision--National Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC is responsible for administering and monitoring the National
Program of Cancer Registries (NPCR). The NPCR provides technical
assistance and funding and sets program standards to assure that
complete local, state, regional, and national cancer incidence data are
available for national and state cancer control and prevention
activities and health planning activities. As of 2008, CDC supports 49
population-based central cancer registries (CCR) in 45 states, two
territories, the District of Columbia, and the Pacific Islands. The
National Cancer Institute supports the operations of CCRs in the five
remaining states.
Cancer registries currently submit information about registry
operations to CDC on an annual basis via a secure, web-based Annual
Program Evaluation Instrument (APEI) (OMB 0920-0706, exp. 12/31/2008).
During the next OMB approval period, CDC proposes to change the data
collection frequency from annual to every other year, with data
collection occurring only in odd-numbered years. This change will
reduce burden to respondents. The project title and the instrument will
be revised to reflect the change in data collection frequency (from
National Program of Cancer Registries Annual Program Evaluation
Instrument (NPCR-APEI) to National Program of Cancer Registries Program
Evaluation Instrument (NPCR-PEI)).
The Program Evaluation Instrument (NCPR-PEI) includes questions
about the following categories of registry operations: (1) Staffing,
(2) legislation, (3) administration, (4) reporting completeness, (5)
data exchange, (6) data content and format, (7) data quality assurance,
(8) data use, (9) collaborative relationships, (10) advanced
activities, (11) ``success stories'' that summarize ways in which CCR
data are used, and (12) survey feedback. Examples of information that
can be obtained from various questions include, but are not limited to:
(1) Number of filled full-time staff positions by position
responsibility; (2) legislation protecting the confidentiality of CCR
data; (3) data quality control activities; (4) data collection
activities as they relate to achieving NPCR standards for data
completeness; and (5) whether or not registry data are used for
comprehensive cancer control programs, needs assessment/program
planning, clinical studies, or incidence and mortality estimates.
The NPCR-PEI is needed in order to receive, process, evaluate,
aggregate, and disseminate NPCR program information. The information is
used by CDC and the NPCR-funded registries to monitor progress toward
meeting established program standards, goals, and objectives; to
evaluate various attributes of the registries funded by NPCR; and to
respond to data inquiries made by CDC and other agencies of the federal
government.
CDC requests OMB approval for a period of three years to collect
information in the summer of 2009 and the summer of 2011. There are no
costs to respondents except their time.
The estimated annualized burden hours are summarized in the table
below.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondents Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
NPCR Grantees................................... 33 1 1.5 50
----------------------------------------------------------------------------------------------------------------
Dated: June 13, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-14152 Filed 6-20-08; 8:45 am]
BILLING CODE 4163-18-P
