Submission for OMB Review; Comment Request; Multi-Ethnic Study of Atherosclerosis (MESA) Event Surveillance, 63488-63489 [2010-26030]
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63488
Federal Register / Vol. 75, No. 199 / Friday, October 15, 2010 / Notices
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 8–1099, One Choke Cherry Road,
Rockville, MD 20857 AND e-mail a copy
to summer.king@samhsa.hhs.gov.
Written comments should be received
within 30 days of this notice.
Dated: October 8, 2010.
Elaine Parry,
Director, Office of Management, Technology
and Operations.
[FR Doc. 2010–26077 Filed 10–14–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Child Care and Development
Block Grant Reporting Requirements—
ACF–700.
OMB No.: 0980–0241.
Description: The Child Care and
Development Fund (CCDF) report
requests annual Tribal aggregate
information on services provided
through the CCDF, which is required by
the CCDF Final Rule (45 FR parts 98 and
99). Tribal Lead Agencies (TLAs) are
required to submit annual aggregate data
appropriate to Tribal programs on
children and families receiving CCDFfunded child care services. The CCDF
statute and regulations also require
TLAs to submit a supplemental
narrative as part of the ACF–700 report.
This narrative describes child care
activities and actions in the TLA’s
service area. Information from the ACF–
700 and supplemental narrative report
will be included in the Secretary’s
Report to Congress, as appropriate, and
will be shared with all TLAs to inform
them of CCDF-funded activities in other
Tribal programs.
Respondents: Tribal Governments.
ANNUAL BURDEN ESTIMATES
Instrument
Number of respondents
Number of responses per
respondent
Average burden hours per
response
Total burden
hours
ACF–700 Report ..............................................................................................
260
1
38
9,880
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Estimated Total Annual Burden
Hours: 9,880
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Administration, Office of Information
Services, 370 L’Enfant Promenade, SW.,
Washington, DC 20447, Attn: ACF
Reports Clearance Officer. All requests
should be identified by the title of the
information collection. E-mail address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7285,
E-mail:
OIRA_SUBMISSION@OMB.EOP.GOV,
Attn: Desk Officer for the
Administration for Children and
Families.
Dated: October 12, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–26052 Filed 10–14–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review;
Comment Request; Multi-Ethnic Study
of Atherosclerosis (MESA) Event
Surveillance
Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Heart, Lung, and Blood Institute
(NHLBI), the National Institutes of
Health (NIH) has submitted to the Office
of Management and Budget (OMB) a
request for review and approval the
information collection listed below.
This proposed information collection
was previously published in the Federal
Register on August 4, 2010, pages
46945–6, and allowed 60-days for
public comment. Only one comment
was received. The purpose of this notice
is to allow an additional 30 days for
public comment. The National Institutes
of Health may not conduct or sponsor,
and the respondent is not required to
respond to, an information collection
that has been extended, revised, or
implemented on or after October 1,
1995, unless it displays a currently valid
OMB control number.
Proposed Collection: Title: MultiEthnic Study of Atherosclerosis (MESA)
Event Surveillance. Type of Information
Request: Renewal (OMB No. 0925–
SUMMARY:
PO 00000
Frm 00056
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0493). Need and Use of Information
Collection: The study, MESA, is
identifying and quantifying factors
associated with the presence and
progression of subclinical
cardiovascular disease (CVD)—that is,
atherosclerosis and other forms of CVD
that have not produced signs and
symptoms. The findings provide
important information on subclinical
CVD in individuals of different ethnic
backgrounds and provide information
for studies on new interventions to
prevent CVD. The aspects of the study
that concern direct participant
evaluation received a clinical exemption
from OMB clearance (CE–99–11–08) in
April 2000. OMB clearance is being
sought for the contact of physicians and
participant proxies to obtain
information about clinical CVD events
that participants experience during the
follow-up period. Frequency of
response: Once per CVD event. Affected
public: Individuals. Types of
Respondents: Physicians and selected
proxies of individuals recruited for
MESA. The annual reporting burden is
as follows: Estimated Number of
Respondents: 74; Estimated Number of
Responses per Respondent: 1.0; Average
Burden Hours Per Response: 0.20; and
Estimated Total Annual Burden Hours
Requested: 14.7. The annualized cost to
respondents is estimated at: $500. There
are no capital, operating, or
maintenance costs to report.
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Federal Register / Vol. 75, No. 199 / Friday, October 15, 2010 / Notices
Estimated
number of
respondents
Type of respondents
Estimated
number of
responses per
respondent
Average
burden hours
per response
Estimated
total annual
burden hours
requested
Physicians ........................................................................................................
Proxies .............................................................................................................
17
57
1.0
1.0
0.20
0.20
3.4
11.3
Total ..........................................................................................................
74
1.0
0.20
14.7
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Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Whether the proposed collection of
information will have practical utility;
(2) The accuracy of the agency’s
estimate of burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
Ways to minimize the burden of
collection of information on those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Direct Comments to OMB: Written
comments and/or suggestions regarding
the item(s) contained in this notice,
especially regarding the estimated
public burden and associated response
time, should be directed to the: Office
of Management and Budget, Office of
Regulatory Affairs,
OIRA_submission@omb.eop.gov or by
fax to 202–395–6974, Attention: Desk
Officer for NIH. To request more
information on the proposed project or
to obtain a copy of the data collection
plans and instruments, contact: Dr.
Diane Bild, Division of Cardiovascular
Sciences, NHLBI, NIH, II Rockledge
Centre, 6701 Rockledge Drive, Suite
10122, MSC #7936, Bethesda, MD
20892–7934, or call non-toll-free
number (301) 435–0457 or E-mail your
request, including your address to:
bildd@nhlbi.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30 days of the date of
this publication.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
National Institutes of Health
[Docket No. FDA–2009–N–0380]
Proposed Collection; Comment
Request; NIH Office of Intramural
Training & Education Application
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Product Jurisdiction: Assignment of
Agency Component for Review of
Premarket Applications
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Product Jurisdiction: Assignment of
Agency Component for Review of
Premarket Applications’’ has been
approved by the Office of Management
and Budget (OMB) under the Paperwork
Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Jonna Capezzuto, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3794,
Jonnalynn.capezzuto@fda.hhs.gov.
SUMMARY:
In the
Federal Register of March 17, 2010 (75
FR 12758), the agency announced that
the proposed information collection had
been submitted to OMB for review and
clearance under 44 U.S.C. 3507. An
agency may not conduct or sponsor, and
a person is not required to respond to,
a collection of information unless it
displays a currently valid OMB control
number. OMB has now approved the
information collection and has assigned
OMB control number 0910–0523. The
approval expires on August 31, 2013. A
copy of the supporting statement for this
information collection is available on
the Internet at https://www.reginfo.gov/
public/do/PRAMain.
SUPPLEMENTARY INFORMATION:
Suzanne Freeman,
NHLBI Project Clearance Liaison, National
Institutes of Health.
Michael Lauer,
Director, DCVS, National Institutes of Health.
Dated: October 8, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–26030 Filed 10–14–10; 8:45 am]
[FR Doc. 2010–25975 Filed 10–14–10; 8:45 am]
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Under the provisions of
Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the Office of
Intramural Training & Education, the
National Institutes of Health (NIH) has
submitted to the Office of Management
and Budget (OMB) a request for review
and approval of the information
collection listed below. This proposed
information collection was previously
published in the Federal Register on
July 20, 2010 (Vol. 75, No. 138 on pages
42097–42098) and allowed 60 days for
public comment. No public comments
were received. The purpose of this
notice is to allow an additional 30 days
for public comment. The National
Institutes of Health may not conduct or
sponsor, and the respondent is not
required to respond to, an information
collection that has been extended,
revised, or implemented on or after
October 1, 1995, unless it displays a
currently valid OMB control number.
Proposed Collection: Title: NIH Office
of Intramural Training & Education
Application. Type of Information
Collection Request: Revision. Need and
Use of Information Collection: The
Office of Intramural Training &
Education (OITE) administers a variety
of programs and initiatives to recruit
pre-college through post-doctoral
educational level individuals into the
National Institutes of Health Intramural
Research Program (NIH–IRP) to facilitate
develop into future biomedical
scientists. The proposed information
collection is necessary in order to
determine the eligibility and quality of
potential awardees for traineeships in
these programs. The applications for
admission consideration include key
areas such as: Personal information,
eligibility criteria, contact information,
student identification number, training
program selection, scientific discipline
interests, educational history,
standardized examination scores,
reference information, resume
SUMMARY:
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[Federal Register Volume 75, Number 199 (Friday, October 15, 2010)]
[Notices]
[Pages 63488-63489]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-26030]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; Comment Request; Multi-Ethnic Study of
Atherosclerosis (MESA) Event Surveillance
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National Heart, Lung, and Blood Institute
(NHLBI), the National Institutes of Health (NIH) has submitted to the
Office of Management and Budget (OMB) a request for review and approval
the information collection listed below. This proposed information
collection was previously published in the Federal Register on August
4, 2010, pages 46945-6, and allowed 60-days for public comment. Only
one comment was received. The purpose of this notice is to allow an
additional 30 days for public comment. The National Institutes of
Health may not conduct or sponsor, and the respondent is not required
to respond to, an information collection that has been extended,
revised, or implemented on or after October 1, 1995, unless it displays
a currently valid OMB control number.
Proposed Collection: Title: Multi-Ethnic Study of Atherosclerosis
(MESA) Event Surveillance. Type of Information Request: Renewal (OMB
No. 0925-0493). Need and Use of Information Collection: The study,
MESA, is identifying and quantifying factors associated with the
presence and progression of subclinical cardiovascular disease (CVD)--
that is, atherosclerosis and other forms of CVD that have not produced
signs and symptoms. The findings provide important information on
subclinical CVD in individuals of different ethnic backgrounds and
provide information for studies on new interventions to prevent CVD.
The aspects of the study that concern direct participant evaluation
received a clinical exemption from OMB clearance (CE-99-11-08) in April
2000. OMB clearance is being sought for the contact of physicians and
participant proxies to obtain information about clinical CVD events
that participants experience during the follow-up period. Frequency of
response: Once per CVD event. Affected public: Individuals. Types of
Respondents: Physicians and selected proxies of individuals recruited
for MESA. The annual reporting burden is as follows: Estimated Number
of Respondents: 74; Estimated Number of Responses per Respondent: 1.0;
Average Burden Hours Per Response: 0.20; and Estimated Total Annual
Burden Hours Requested: 14.7. The annualized cost to respondents is
estimated at: $500. There are no capital, operating, or maintenance
costs to report.
[[Page 63489]]
----------------------------------------------------------------------------------------------------------------
Estimated Estimated
Estimated number of Average total annual
Type of respondents number of responses per burden hours burden hours
respondents respondent per response requested
----------------------------------------------------------------------------------------------------------------
Physicians...................................... 17 1.0 0.20 3.4
Proxies......................................... 57 1.0 0.20 11.3
---------------------------------------------------------------
Total....................................... 74 1.0 0.20 14.7
----------------------------------------------------------------------------------------------------------------
Request for Comments: Written comments and/or suggestions from the
public and affected agencies are invited on one or more of the
following points: (1) Whether the proposed collection of information
will have practical utility; (2) The accuracy of the agency's estimate
of burden of the proposed collection of information, including the
validity of the methodology and assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the information to be collected;
and (4) Ways to minimize the burden of collection of information on
those who are to respond, including the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology.
Direct Comments to OMB: Written comments and/or suggestions
regarding the item(s) contained in this notice, especially regarding
the estimated public burden and associated response time, should be
directed to the: Office of Management and Budget, Office of Regulatory
Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974,
Attention: Desk Officer for NIH. To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact: Dr. Diane Bild, Division of Cardiovascular
Sciences, NHLBI, NIH, II Rockledge Centre, 6701 Rockledge Drive, Suite
10122, MSC 7936, Bethesda, MD 20892-7934, or call non-toll-
free number (301) 435-0457 or E-mail your request, including your
address to: bildd@nhlbi.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 30 days
of the date of this publication.
Suzanne Freeman,
NHLBI Project Clearance Liaison, National Institutes of Health.
Michael Lauer,
Director, DCVS, National Institutes of Health.
[FR Doc. 2010-26030 Filed 10-14-10; 8:45 am]
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