Agency Forms Undergoing Paperwork Reduction Act Review, 33432-33433 [E8-13181]
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33432
Federal Register / Vol. 73, No. 114 / Thursday, June 12, 2008 / Notices
FEDERAL RETIREMENT THRIFT
INVESTMENT BOARD
Employee Thrift Advisory Council
9 a.m. (Eastern Time),
June 30, 2008.
PLACE: 2nd Floor, Training Room, 1250
H Street, NW., Washington, DC 20005.
STATUS: Open.
MATTERS TO BE CONSIDERED:
1. Approval of the minutes of the
December 19, 2007 meeting.
2. Report of the Executive Director on
Thrift Savings Plan Status.
3. Discussion Draft Legislation.
4. Other proposals.
5. New business.
FOR FURTHER INFORMATION CONTACT:
Thomas K. Emswiler, Committee
Management Officer, (202) 942–1660.
TIME AND DATE:
Dated: June 10, 2008.
Thomas K. Emswiler,
General Counsel, Federal Retirement Thrift
Investment Board.
[FR Doc. 08–1353 Filed 6–10–08; 1:59 pm]
BILLING CODE 6760–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Pediatric Medical Device Stakeholders
Workshop
Agency for Healthcare
Research and Quality (AHRQ); U.S.
Food and Drug Administration (FDA);
and National Institutes of Health (NIH).
ACTION: Notice.
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AGENCIES:
SUMMARY: The Interagency (AHRQ–
FDA–NIH) Pediatric Devices Working
Group is holding a workshop to gather
information about the development of
pediatric devices.
DATES: The workshop will be held on
July 23, 2008 from 8 a.m. until 5 p.m.
EDT.
ADDRESSES: The workshop will be held
in Natcher Auditorium, located in
Building 45, NIH Main Campus,
Bethesda, Maryland 20814.
FOR FURTHER INFORMATION CONTACT:
Steven Hirschfeld, MD, PhD, Associate
Director for Clinical Research, Eunice
Kennedy Shriver National Institute of
Child Health and Human Development,
31 Center Drive, Room 2A03, Bethesda,
Maryland 20814; Tel: 301–496–3454;
Fax: 301–402–1104; E-mail:
hirschfs@mail.nih.gov.
In
September 2007, the Congress passed
Title III of the FDA Amendments Act,
called the Pediatric Medical Device
Safety and Improvement Act. The
SUPPLEMENTARY INFORMATION:
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legislation requires that the DHHS
Secretary submit a plan to Congress for
expanding pediatric medical device
research and development. In
developing the plan, the DHHS
Secretary shall consult with individuals
and organizations with appropriate
expertise in pediatric medical devices.
The plan shall include the current status
of federally funded pediatric medical
device research; any gaps in such
research, which may include a survey of
pediatric medical providers regarding
unmet pediatric medical device needs,
as needed; and a research agenda for
improving pediatric medical device
development and Food and Drug
Administration clearance or approval of
pediatric medical devices, and
evaluating the short- and long-term
safety and effectiveness of pediatric
medical devices.
This meeting of the Interagency
Pediatric Devices Working Group,
which includes AHRQ, FDA, and NIH,
seeks to elicit feedback about expanding
pediatric device research and
development from interested
communities and the public to help
inform the plan that the DHHS Secretary
will submit in accordance with the
legislation.
The purpose of this workshop is to:
• Inform the community of the
current status of pediatric device
development;
• Describe available mechanisms for
device product registration;
• Describe available mechanisms for
pediatric device project funding;
• Understand what stakeholders see
to be important areas of study;
• Determine gaps in knowledge and
where the needs for research are; and
• Discuss ways to gather the
information needed to move ahead,
such as overcoming barriers, handling
logistics, determining classes of devices
to study, and identifying available
databases, registries, surveillance
systems.
You are not required to preregister for
this meeting to attend. However,
preregistering allows you to receive
current information about the meeting,
its agenda, and other details (such as
how to prepare statements, participating
in working lunch sessions, etc.). To
register, please send an e-mail to
hirschfs@mail.nih.gov with ‘‘Device
Workshop Registration’’ in the subject
line. Please also include the following
information. (Note: Incomplete
information may limit the organizers’
ability to keep you informed about the
workshop; please provide accurate and
complete information):
• First and Last Name
• Degree (optional)
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• Professional Title (optional)
• Organization and Department
• Type of Organization (e.g.,
government agency, non-profit hospital,
for-profit company, etc.)
• Address
• City, State, and ZIP Code
• Country
• Phone (Main contact number):
• Fax:
• E-mail:
The agenda; logistics; legislation;
background material and information;
and a link to the Request for Information
(RFI) issued for this topic can be found
at https://www.nichd.nih.gov/about/
meetings/2008/devices.cfm.
Duane Alexander,
Director, Eunice Kennedy Shriver Institute of
Child Health and Human Development,
National Institutes of Health.
[FR Doc. E8–13278 Filed 6–11–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–08–07BJ]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an
e-mail to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
Economic Analysis of the National
Program of Cancer Registries—New—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The National Program of Cancer
Registries (NPCR) is a comprehensive,
federally sponsored public health
program involving cancer registries in
45 States and the District of Columbia.
The NPCR was established to collect
data on the occurrence of cancer; the
type, extent, and location of the cancer;
and the type of initial treatment.
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12JNN1
33433
Federal Register / Vol. 73, No. 114 / Thursday, June 12, 2008 / Notices
CDC proposes to conduct a systematic
analysis of the economic costs incurred
by the NPCR. Additional information
will be collected on registry activities,
activity-based costs, other sources of
funding and in-kind contributions.
Information will be submitted to CDC
once per year for three years using a
Web-based system. There is no overlap
with information currently collected
from NPCR awardees through the
Annual Program Evaluation Instrument
(OMB No. 0920–0706, exp. 12/31/2008).
The proposed information collection
will allow CDC to assess the true cost of
registry operations in relation to the
benefits of those operations, identify
factors that impact cost, perform costeffectiveness analysis, and improve the
efficiency of resource allocation within
the NPCR.
There are no costs to respondents
except their time. The total estimated
annualized burden hours are 1,012.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
NPCR funded registries ...............................................................................................................
Dated: June 5, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–13181 Filed 6–11–08; 8:45 am]
BILLING CODE 4163–18–P
Proposed Project
2009 and 2011 National Youth
Tobacco Surveys (NYTS)—Revision—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–08–0621]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an
e-mail to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
CDC requests OMB approval to
conduct the National Youth Tobacco
Survey (NYTS) in 2009 and 2011 (OMB
No. 0920–0621; exp. date December 31,
2008). The NYTS is a school-based
survey that that has been conducted in
1999, 2000, 2002, 2004, and 2006. To
improve the coordination and efficiency
of school-based surveillance activities
within CDC, the proposed revision will
establish a routine data collection
schedule to occur in the Spring of oddnumbered years. Minor changes to the
survey instrument and the burden
estimate also are proposed.
The NYTS provides national
estimates for middle and high school
students of tobacco use behaviors,
information about exposure to pro- and
anti-tobacco influences, and information
about racial and ethnic disparities in
these tobacco-related behaviors and
behavioral determinants. Information
collected through the NYTS is used to
46
Number of
responses per
respondent
1
Average
burden per
response
(in hours)
22
identify trends over time, to inform the
development of tobacco cessation
programs for youth, and to evaluate the
effectiveness of existing interventions
and programs. The NYTS covers the
following topics related to youth
tobacco use: Use of cigarettes, smokeless
tobacco, cigars, pipes, bidis, and
kreteks; knowledge and attitudes; media
and advertising; access to tobacco
products and enforcement of restrictions
on access; school curriculum;
environmental tobacco smoke exposure;
and cessation.
The NYTS will be conducted among
nationally representative samples of
students in grades 6–12 attending public
and private schools. Responding
students will complete a selfadministered optically scannable
questionnaire that includes multiplechoice questions. Information
supporting the NYTS also will be
collected from state-, district-, and
school-level administrators and
teachers. The table below reports the
combined total number of respondents
for the 2009 and 2011 NYTS annualized
over the requested three-year OMB
approval period.
There are no costs to respondents
except their time. The estimated
annualized burden hours are 10,213.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
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Type of respondents
Form name
State Administrators ........................................
District Administrators .....................................
School Administrators .....................................
Teachers .........................................................
Students ..........................................................
State-level Recruitment Script for the NYTS
District-level Recruitment Script for the NYTS
School-level Recruitment Script for the NYTS
Data Collection Checklist for the NYTS .........
National Youth Tobacco Survey (NYTS) .......
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17
80
133
635
13,251
12JNN1
Number of
responses per
respondent
1
1
1
1
1
Average
burden per
response
(in hours)
30/60
30/60
30/60
15/60
45/60
Agencies
[Federal Register Volume 73, Number 114 (Thursday, June 12, 2008)]
[Notices]
[Pages 33432-33433]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-13181]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-08-07BJ]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
Economic Analysis of the National Program of Cancer Registries--
New--National Center for Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The National Program of Cancer Registries (NPCR) is a
comprehensive, federally sponsored public health program involving
cancer registries in 45 States and the District of Columbia. The NPCR
was established to collect data on the occurrence of cancer; the type,
extent, and location of the cancer; and the type of initial treatment.
[[Page 33433]]
CDC proposes to conduct a systematic analysis of the economic costs
incurred by the NPCR. Additional information will be collected on
registry activities, activity-based costs, other sources of funding and
in-kind contributions. Information will be submitted to CDC once per
year for three years using a Web-based system. There is no overlap with
information currently collected from NPCR awardees through the Annual
Program Evaluation Instrument (OMB No. 0920-0706, exp. 12/31/2008).
The proposed information collection will allow CDC to assess the
true cost of registry operations in relation to the benefits of those
operations, identify factors that impact cost, perform cost-
effectiveness analysis, and improve the efficiency of resource
allocation within the NPCR.
There are no costs to respondents except their time. The total
estimated annualized burden hours are 1,012.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Respondents respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
NPCR funded registries.......................................... 46 1 22
----------------------------------------------------------------------------------------------------------------
Dated: June 5, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-13181 Filed 6-11-08; 8:45 am]
BILLING CODE 4163-18-P