Agency Forms Undergoing Paperwork Reduction Act Review, 47818-47819 [2010-19555]
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47818
Federal Register / Vol. 75, No. 152 / Monday, August 9, 2010 / Notices
data collected from the updates is also
shared with the Division of Grants
Management Operations (DGMO) for
their assistance in the overall evaluation
of each project’s progress.
An electronic form is currently being
used for progress reporting for the
prior to submission. We acknowledge a
change in the burden estimate due to
close out of old projects, and the
addition of new projects for FY 2010.
The annual estimate of burden is as
follows:
HCOF program. This form provides
awardees access to directly input the
required status update information in a
timely, consistent, and uniform manner.
The electronic form minimizes burden
to respondents and informs respondents
when there are missing data elements
Number of
respondents
Instrument
Responses
per
respondent
Total
responses
Hours per
response
Total Burden
hours
Construction-Related ...........................................................
Equipment Only ...................................................................
481
1,238
4
1
1,924
1,238
.5
.5
962
619
Total ..............................................................................
1,719
........................
3,162
........................
1,581
Written comments and
recommendations concerning the
proposed information collection should
be sent within 30 days of this notice to
the desk officer for HRSA, either by email to OIRA_submission@omb.eop.gov
or by fax to 202–395–6974. Please direct
all correspondence to the ‘‘attention of
the desk officer for HRSA.’’
Dated: August 3, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information
Coordination.
through student focus groups and
teacher interviews. Students will
complete a participant profile form to
capture basic demographic information.
The specific aim of this study is to
assess whether the Safe Dates
adolescent dating violence prevention
program needs modification/adaptation
for urban, high-risk adolescents.
Approximately 40 students at one
school will participate in focus groups.
Two focus groups will consist of 8–10
boys, and two focus groups will include
8–10 girls. Informed written consent
from parents for each student’s
participation and informed written
assent from tenth graders for their own
participation will be obtained. Twenty
teachers will participate in interviews.
Students and teachers will be asked
about their experiences with the Safe
Dates program and ideas they may have
about adapting the program for urban
schools.
Data collection will occur in July
2010. It is anticipated that study results
will be used to determine whether the
Safe Dates program should be modified
for an urban, high-risk population.
There is no cost to respondents other
than their time. The total estimated
annual burden hours are 849.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
[FR Doc. 2010–19549 Filed 8–6–10; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Evaluation of Safe Dates Project—
(OMB No. 0920–0783 exp. 6/30/2011)—
Revision—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Centers for Disease Control and
Prevention
[30 Day-10–0783]
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.
Safe Dates, a dating violence
prevention curriculum for 8th and 9th
grade students, has been shown to be
effective at preventing victimization and
perpetration of teen dating violence in
one rural North Carolina school district,
but appropriateness of the program with
urban, high-risk adolescents is
unknown. The data collection will
require participation from teachers at
eight schools who delivered the Safe
Dates program and students at one
school who received the program.
Qualitative data will be collected
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondent
Instrument name
Student ..............................................
Effectiveness follow-up survey .........
Focus group guide and participant
profile form.
Interview guide .................................
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Teacher .............................................
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Number of
respondents
Sfmt 4703
Number of
responses per
respondent
Average
burden per
respondent
(in hours)
Total response
burden (hours)
1,318
40
1
1
35/60
1.5
769
60
20
1
1
20
E:\FR\FM\09AUN1.SGM
09AUN1
Federal Register / Vol. 75, No. 152 / Monday, August 9, 2010 / Notices
Dated: August 3, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2010–19555 Filed 8–6–10; 8:45 am]
National Institute on Alcohol Abuse
and Alcoholism; Notice of Closed
Meeting
BILLING CODE 4163–18–P
National Institutes of Health
47819
and Research Support Awards, National
Institutes of Health, HHS)
Dated: July 29, 2010.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2010–19558 Filed 8–6–10; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Center for Substance Abuse
Treatment; Notice of Meeting
Pursuant to Public Law 92–463,
notice is hereby given that the
Substance Abuse and Mental Health
Services Administration’s (SAMHSA)
Center for Substance Abuse Treatment
(CSAT) National Advisory Council will
meet August 19, 2010, 1–3 p.m. via
teleconference.
The meeting will include discussion
and evaluation of grant applications
reviewed by Initial Review Groups.
Therefore, the meeting will be closed to
the public as determined by the
Administrator, SAMHSA, in accordance
with Title 5 U.S.C. 552b(c)(6) and 5
U.S.C. App. 2, Section 10(d).
Substantive program information, a
summary of the meeting and a roster of
Council members may be obtained as
soon as possible after the meeting, either
by accessing the SAMHSA Committee
Web site at https://nac.samhsa.gov/
CSATcouncil/index.aspx, or by
contacting the CSAT National Advisory
Council Designated Federal Official, Ms.
Cynthia Graham (see contact
information below).
sroberts on DSKD5P82C1PROD with NOTICES
Committee Name: SAMHSA’s Center for
Substance Abuse Treatment National
Advisory Council.
Date/Time/Type: August 19, 2010, 1– 3
p.m.: Closed.
Place: SAMHSA Building, 1 Choke Cherry
Road, Great Falls Conference Room,
Rockville, Maryland 20857.
Contact: Cynthia Graham, M.S., Designated
Federal Official, SAMHSA CSAT National
Advisory Council, 1 Choke Cherry Road,
Room 5–1035, Rockville, Maryland 20857,
Telephone: (240) 276–1692, Fax: (240)
276–1690, e-mail:
cynthia.graham@samhsa.hhs.gov.
Dated: August 3, 2010.
Toian Vaughn,
Committee Management Officer, Substance
Abuse and Mental Health, Services
Administration.
[FR Doc. 2010–19539 Filed 8–6–10; 8:45 am]
BILLING CODE 4162–20–P
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Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App), notice is
hereby given of a meeting of the
National Advisory Council on Alcohol
Abuse and Alcoholism.
The meeting will be open to the
public as indicated below, with
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable materials,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Advisory
Council on Alcohol Abuse and Alcoholism.
Date: September 22–23, 2010.
Closed: September 22, 2010, 5:30 p.m. to
7:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 5635
Fishers Lane, Bethesda, MD 20892.
Open: September 23, 2010, 9 a.m. to 3 p.m.
Agenda: Presentations and other business
of the council.
Place: National Institutes of Health, 5635
Fishers Lane, Bethesda, MD 20892.
Contact Person: Abraham P. Bautista, PhD,
Executive Secretary, National Institute on
Alcohol Abuse and Alcoholism, National
Institutes of Health, 5635 Fishers Lane, Room
2085, Rockville, MD 20892, 301–443–9737.
bautistaa@mail.nih.gov.
Information is also available on the
Institute’s/Center’s home page: https:///
www.silk.nih.gov/silk/niaaa1/about/
roster.htm, where an agenda and any
additional information for the meeting will
be posted when available.
(Catalogue of Federal Domestic Assistance
Program Nos.: 93.271, Alcohol Research
Career Development Awards for Scientists
and Clinicians; 93.272, Alcohol National
Research Service Awards for Research
Training; 93.273, Alcohol Research Programs;
93.891, Alcohol Research Center Grants;
93.701, ARRA Related Biomedical Research
PO 00000
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Fmt 4703
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0001]
Workshop on Optimizing Clinical Trial
Design for the Development of
Pediatric Cardiovascular Devices
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of public workshop.
The Food and Drug Administration
(FDA) and National Institutes of Health
(NIH), with support from the American
Academy of Pediatrics (AAP), the
American College of Cardiology (ACC),
and the Society for Cardiovascular
Angiography and Interventions (SCAI)
are announcing a public workshop
entitled ‘‘Optimizing Clinical Trial
Design for the Development of Pediatric
Cardiovascular Devices.’’ The topic to be
discussed is pediatric cardiovascular
device development. The purpose of the
public workshop is to solicit
information from clinicians, academia,
professional societies, other government
agencies, and industry on various
efficient and pragmatic clinical trial
designs that are conducive to
overcoming the challenges in
developing devices for the pediatric
cardiology market. The information
gathered in this and future workshops
will help to develop future guidance on
optimal designs for pediatric cardiology
device trials.
Date and Time: The public workshop
will be held on September 30, 2010,
from 8 a.m. to 5:30 p.m.
Location: The public workshop will
be held at Moscone Center, 747 Howard
St., San Francisco, CA 94103.
Contact Person: Francesca Joseph,
Office of Orphan Products
Development, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 32, rm. 5277, Silver Spring,
MD 20903, 301–796–6805, FAX: 301–
847–8621, e-mail:
francesca.joseph@fda.hhs.gov.
Registration: Registration information
will be posted on the Internet at https://
www.fda.gov/MedicalDevices/
NewsEvents/WorkshopsConferences/
default.htm.
E:\FR\FM\09AUN1.SGM
09AUN1
]]>Agencies
[Federal Register Volume 75, Number 152 (Monday, August 9, 2010)]
[Notices]
[Pages 47818-47819]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-19555]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30 Day-10-0783]
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) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
Evaluation of Safe Dates Project--(OMB No. 0920-0783 exp. 6/30/
2011)--Revision--National Center for Injury Prevention and Control
(NCIPC), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Safe Dates, a dating violence prevention curriculum for 8th and 9th
grade students, has been shown to be effective at preventing
victimization and perpetration of teen dating violence in one rural
North Carolina school district, but appropriateness of the program with
urban, high-risk adolescents is unknown. The data collection will
require participation from teachers at eight schools who delivered the
Safe Dates program and students at one school who received the program.
Qualitative data will be collected through student focus groups and
teacher interviews. Students will complete a participant profile form
to capture basic demographic information. The specific aim of this
study is to assess whether the Safe Dates adolescent dating violence
prevention program needs modification/adaptation for urban, high-risk
adolescents.
Approximately 40 students at one school will participate in focus
groups. Two focus groups will consist of 8-10 boys, and two focus
groups will include 8-10 girls. Informed written consent from parents
for each student's participation and informed written assent from tenth
graders for their own participation will be obtained. Twenty teachers
will participate in interviews. Students and teachers will be asked
about their experiences with the Safe Dates program and ideas they may
have about adapting the program for urban schools.
Data collection will occur in July 2010. It is anticipated that
study results will be used to determine whether the Safe Dates program
should be modified for an urban, high-risk population. There is no cost
to respondents other than their time. The total estimated annual burden
hours are 849.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Instrument name Number of responses per per respondent Total response
respondents respondent (in hours) burden (hours)
----------------------------------------------------------------------------------------------------------------
Student....................... Effectiveness 1,318 1 35/60 769
follow-up
survey.
Focus group 40 1 1.5 60
guide and
participant
profile form.
Teacher....................... Interview guide. 20 1 1 20
----------------------------------------------------------------------------------------------------------------
[[Page 47819]]
Dated: August 3, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2010-19555 Filed 8-6-10; 8:45 am]
BILLING CODE 4163-18-P
