Agency Information Collection Activities: Submission for OMB Review; Comment Request, 62475-62476 [E6-17812]
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Federal Register / Vol. 71, No. 206 / Wednesday, October 25, 2006 / Notices
epilepsy; (3) directs and administers the
development of a national, state, and
local surveillance system of tracking
health-related quality of life (HRQOL)
among U.S. residents; (4) administers
grants, cooperative agreements,
contracts, and other procurement
requests to implement evidence-based
health promotion interventions and
disseminate arthritis prevention and
epilepsy education messages; (5)
develops, validates, and refines HRQOL
measure for use in tracking and
prevention research at each life stage;
(6) directs and coordinates the
evaluation of community and statebased intervention programs for arthritis
and epilepsy; (7) developes arthritis
epidemiology capacity and other
arthritis programmatic capabilities in
state health department settings; and (8)
disseminates health promotion and
disease prevention information through
national advocacy partners for arthritis
and epilepsy.
Dated: October 12, 2006.
William H. Gimson,
Chief Operating Officer, Centers for Disease
Control and Prevention (CDC).
[FR Doc. 06–8869 Filed 10–24–06; 8:45 am]
BILLING CODE 4160–18–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006F–0409]
Safe Foods Corporation; Filing of Food
Additive Petition
AGENCY:
Food and Drug Administration,
HHS.
mstockstill on PROD1PC61 with NOTICES
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that Safe Foods Corporation has filed a
petition proposing that the food additive
regulations be amended to expand the
conditions for the safe use of
cetylpyridinium chloride as an
antimicrobial agent in a pre-chiller or
post-chiller solution for application to
raw poultry carcasses.
DATES: Submit written or electronic
comments on the petitioner’s
environmental assessment by November
24, 2006.
ADDRESSES: Submit written comments
to the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
VerDate Aug<31>2005
15:12 Oct 24, 2006
Jkt 211001
1061, Rockville, MD 20852. Submit
electronic comments to https://
www.fda.gov/dockets/ecomments.
FOR FURTHER INFORMATION CONTACT:
Raphael Davy, Center for Food Safety
and Applied Nutrition (HFS–265), Food
and Drug Administration, 5100 Paint
Branch Pkwy., College Park, MD 20740,
301–436–1272.
SUPPLEMENTARY INFORMATION: Under the
Federal Food, Drug, and Cosmetic Act
(section 409(b)(5) (21 U.S.C. 348(b)(5))),
notice is given that a food additive
petition (FAP 6A4767) has been filed by
Safe Foods Corporation, c/o Keller and
Heckman LLP, 1001 G St. NW., suite
500 West, Washington, D.C. 20001. The
petition proposes to amend the food
additive regulations in § 173.375
Cetylpyridinium chloride (21 CFR
173.375) to expand the conditions for
the safe use of cetylpyridinium chloride
as an antimicrobial agent in a pre-chiller
or post-chiller solution for application
to raw poultry carcasses.
The potential environmental impact
of this action is being reviewed. To
encourage public participation
consistent with regulations issued under
the National Environmental Policy Act
(40 CFR 1501.4(b)), the agency is
placing the environmental assessment
submitted with the petition that is the
subject of this notice on public display
at the Division of Dockets Management
(see ADDRESSES) for public review and
comment. Interested persons may
submit to the Division of Dockets
Management written or electronic
comments by (see DATES). Two copies of
any written comments are to be
submitted, except that individuals may
submit one copy. Comments are to be
identified with the docket number
found in brackets in the heading of this
document. Received comments may be
seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday. FDA will also
place on public display any
amendments to, or comments on, the
petitioner’s environmental assessment
without further announcement in the
Federal Register. If, based on its review,
the agency finds that an environmental
impact statement is not required, and
this petition results in a regulation, the
notice of availability of the agency’s
finding of no significant impact and the
evidence supporting that finding will be
published with the regulation in the
Federal Register in accordance with 21
CFR 25.51(b).
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Fmt 4703
Sfmt 4703
62475
Dated: October 17, 2006.
Laura M. Tarantino,
Director, Office of Food Additive Safety,
Center for Food Safety and Applied Nutrition.
[FR Doc. E6–17834 Filed 10–24–06; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources
and Services Administration (HRSA)
publishes abstracts of information
collection requests under review by the
Office of Management and Budget
(OMB), in compliance with the
Paperwork Reduction Act of 1995 (44
U.S.C. Chapter 35). To request a copy of
the clearance requests submitted to
OMB for review, call the HRSA Reports
Clearance Office on (301)–443–1129.
The following request has been
submitted to the Office of Management
and Budget for review under the
Paperwork Reduction Act of 1995:
Proposed Project: Grants for Hospital
Construction and Modernization—
Federal Right of Recovery and Waiver
of Recovery (42 CFR Part 124, Subpart
H) (OMB No. 0915–0099Extension)
The regulation known as ‘‘Federal
Right of Recovery and Waiver of
Recovery,’’ provides a means for the
Federal Government to recover grant
funds and a method of calculating
interest when a grant-assisted facility
under Titles VI and XVI of the Public
Health Service Act is sold or leased, or
there is a change in use of the facility.
It also allows for a waiver of the right
of recovery under certain circumstances.
Facilities are required to provide written
notice to the Federal Government when
such a change occurs and to provide
copies of sales contracts, lease
agreements, estimates of current assets
and liabilities, value of equipment,
expected value of land on the new
owner’s books and remaining
depreciation for all fixed assets involved
in the transactions, and other
information and documents pertinent to
the change of status.
Estimates of annualized burden are as
follows:
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62476
Federal Register / Vol. 71, No. 206 / Wednesday, October 25, 2006 / Notices
Number of
respondents
Reporting requirements
Reporting requirements 124.704(b) and 707 ............
Written comments and
recommendations concerning the
proposed information collection should
be sent within 30 days of this notice to:
John Kraemer, Human Resources and
Housing Branch, Office of Management
and Budget, New Executive Office
Building, Room 10235, Washington, DC
20503.
Dated: October 17, 2006.
Cheryl R. Dammons,
Director, Division of Policy Review and
Coordination.
[FR Doc. E6–17812 Filed 10–24–06; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; Comment
Request; The Jackson Heart Study
(JHS)
SUMMARY: 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
National Heart, Lung, and Blood
Institute (NHLBI), the National
Institutes of Health (NIH) will publish
periodic summaries of proposed
projects to be submitted to the Office of
Responses per
respondent
10
Hours per
response
Total responses
1
10
Management and Budget (OMB) for
review and approval.
Proposed Collection
Title: The Jackson Heart Study:
Annual Follow-up with Third Party
Respondents.
Type of Information Collection
Request: Revision of a currently
approved collection (OMB NO. 0925–
0491).
Need and Use of Information
Collection: This project involves annual
follow-up by telephone of participants
in the JHS study, review of their
medical records, and interviews with
doctors and family to identify disease
occurrence. Interviewers will contact
doctors and hospitals to ascertain
participants’ cardiovascular events.
Information gathered will be used to
further describe the risk factors,
occurrence rates, and consequences of
cardiovascular disease in African
American men and women. Recruitment
of 5,500 JHS participants began in
September 2000 and was completed in
March 2004. 5,302 participants
completed a baseline Exam 1 that
included demographics, psychosocial
inventories, medical history,
anthropometry, resting and ambulatory
blood pressure, phlebotomy and 24hour urine collection, ECG,
echocardiography, and pulmonary
function. JHS Exam 2 began September
26 2005, with a more comprehensive
Total burden
hours
1.25
12.5
Exam 3 beginning in February 2009. The
two new exams include some repeated
measures from Exam 1 and several new
components, including distribution of
self-monitoring blood pressure devices.
The continuation of the study allows
continued assessment of subclinical
coronary disease, left ventricular
dysfunction, progression of carotid
atherosclerosis and left ventricular
hypertrophy, and responses to stress,
racism, and discrimination as well as
new components such as renal disease,
body fat distribution and body
composition, and metabolic
consequences of obesity.
Frequency of Response: One-time.
Affected Public: Individuals or
households; Businesses or other for
profit; not-for-profit institutions.
Type of Respondents: Middle aged
and elderly adults; doctors and staff of
hospitals and nursing homes. The
annual reporting burden is as follows:
Estimated Number of Respondents:
600;
Estimated Number of Responses per
Respondent: 1.0;
Average Burden Hours per Response:
0.5; and
Estimated Total Annual Burden
Hours Requested: 300.
The annualized cost to respondents is
estimated at $6,500. There are no
Capital Costs to report. There are no
Operating or Maintenance Costs to
report.
ESTIMATE OF ANNUAL HOUR BURDEN
Number of
respondents
Type of response
Frequency of
response
Average
time per
response
Annual hour
burden
200
200
1
1
0.17
0.25
34
50
Total ..........................................................................................................
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Morbidity & Mortality AFU 3rd Party/Next-of-kin decedents ............................
Morbidity & Mortality AFU 3rd Party Physicians .............................................
400
........................
........................
84
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 is necessary for the proper
performance of the function of the
agency, including whether the
information will have practical utility;
(2) The accuracy of the agency’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
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15:12 Oct 24, 2006
Jkt 211001
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 the
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.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
PO 00000
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Fmt 4703
Sfmt 4703
the data collection plans and
instruments, contact Ms. Cheryl Nelson,
Project Officer, NIH, NHLBI, 6701
Rockledge Drive, MSC 7934, Bethesda,
MD 20892–7934, or call non-toll-free
number 301–435–0451 or E-mail your
request, including your address to:
NelsonC@nhlbi.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60-days of the date of
this publication.
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]]>Agencies
[Federal Register Volume 71, Number 206 (Wednesday, October 25, 2006)]
[Notices]
[Pages 62475-62476]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-17812]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
Periodically, the Health Resources and Services Administration
(HRSA) publishes abstracts of information collection requests under
review by the Office of Management and Budget (OMB), in compliance with
the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request
a copy of the clearance requests submitted to OMB for review, call the
HRSA Reports Clearance Office on (301)-443-1129.
The following request has been submitted to the Office of
Management and Budget for review under the Paperwork Reduction Act of
1995:
Proposed Project: Grants for Hospital Construction and Modernization--
Federal Right of Recovery and Waiver of Recovery (42 CFR Part 124,
Subpart H) (OMB No. 0915-0099Extension)
The regulation known as ``Federal Right of Recovery and Waiver of
Recovery,'' provides a means for the Federal Government to recover
grant funds and a method of calculating interest when a grant-assisted
facility under Titles VI and XVI of the Public Health Service Act is
sold or leased, or there is a change in use of the facility. It also
allows for a waiver of the right of recovery under certain
circumstances. Facilities are required to provide written notice to the
Federal Government when such a change occurs and to provide copies of
sales contracts, lease agreements, estimates of current assets and
liabilities, value of equipment, expected value of land on the new
owner's books and remaining depreciation for all fixed assets involved
in the transactions, and other information and documents pertinent to
the change of status.
Estimates of annualized burden are as follows:
[[Page 62476]]
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Total burden
Reporting requirements respondents respondent Total responses response hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Reporting requirements 124.704(b) and 707.......................... 10 1 10 1.25 12.5
--------------------------------------------------------------------------------------------------------------------------------------------------------
Written comments and recommendations concerning the proposed
information collection should be sent within 30 days of this notice to:
John Kraemer, Human Resources and Housing Branch, Office of Management
and Budget, New Executive Office Building, Room 10235, Washington, DC
20503.
Dated: October 17, 2006.
Cheryl R. Dammons,
Director, Division of Policy Review and Coordination.
[FR Doc. E6-17812 Filed 10-24-06; 8:45 am]
BILLING CODE 4165-15-P
