Submission for OMB Review; Comment Request, 49464-49465 [E8-19220]
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49464
Federal Register / Vol. 73, No. 163 / Thursday, August 21, 2008 / Notices
Exhibit 2 shows the estimated
annualized cost burden for the
respondents. The Bureau of Labor
Statistics reported that the average
hourly wage for ‘‘healthcare practitioner
and technical occupations’’ in the
United States was $29.82 in May 2006.
An estimate of $30 per hour allows for
inflation and represents a conservative
estimate of the wages of the
respondents. Therefore, the total
estimated cost burden for respondents is
$12,030, based on the total estimated
annualized burden of 401 hours.
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
Form name
Total burden
hours
Average hourly wage rate *
Total cost
burden
E-mail submission ............................................................................................
Health care innovator interview—following e-mail submission .......................
Health care innovator interview without e-mail submission ............................
Annual follow-up interview ...............................................................................
41
41
234
250
21
21
234
125
$30
30
30
30
$630
630
7,020
3,750
Total ..........................................................................................................
566
401
........................
12,030
* Based upon the average wages, ‘‘National Compensation Survey: Occupational Wages in the United States, May 2006,’’ U.S. Department of
Labor, Bureau of Labor Statistics.
Estimated Annual Costs to the Federal
Government
The total cost to the Government is
approximately $3,349,560 over three
years (on average, $1,116,520 per year).
These costs cover the total editorial and
content development processes
associated with the project; which
include developing an on-line authoring
tool for preparing the profiles,
identifying innovation leads, reviewing
e-mail submissions, contacting the
innovators, conducting interviews,
preparing the draft profiles, securing
innovator approval, and publishing the
profiles on the Innovations Exchange
Web site.
Request for Comments
In accordance with the above-cited
Paperwork Reduction Act legislation,
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) Whether the
proposed collection of information is
necessary for the proper performance of
AHRQ health care research, quality
improvement and information
dissemination functions, including
whether the information will have
practical utility; (b) the accuracy of
AHRQ’s estimate of burden (including
hours and costs) of the proposed
collection(s) 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 upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: August 12, 2008.
Carolyn M. Clancy,
Director.
[FR Doc. E8–19302 Filed 8–20–08; 8:45 am]
BILLING CODE 4160–90–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: State Plan for the Temporary
Assistance for Needy Families (TANF).
OMB No.: 0970–0145.
Description: The State plan is a
mandatory statement submitted to the
Secretary of the Department of Health
and Human Services by the State. It
consists of an outline of how the States
TANF program will be administered
and operated and certain required
certifications by the States Chief
Executive Officer. Its submittal triggers
the States family assistance grant
funding and it is used to provide the
public with information about the
program. If a State makes changes in its
program, it must submit a State plan
amendment.
Respondents: The 50 States, the
District of Columbia, Guam, Puerto Rico
and the Virgin Islands.
ANNUAL BURDEN ESTIMATES
Number of respondents
Number of responses per
respondent
Average burden hours per
response
Total burden
hours
Temporary Assistance to Needy Families State Plan Guidance ....................
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Instrument
54
0.50
33
891
Estimated Total Annual Burden
Hours: 891.
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
VerDate Aug<31>2005
17:48 Aug 20, 2008
Jkt 214001
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
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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: 202–395–6974,
Attn: Desk Officer for the
Administration for Children and
Families.
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Federal Register / Vol. 73, No. 163 / Thursday, August 21, 2008 / Notices
Dated: August 14, 2008.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. E8–19220 Filed 8–20–08; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0039]
Chloramine-T for Control of Bacterial
Gill Disease in Freshwater-Reared
Salmonids; Availability of Data
AGENCY:
Food and Drug Administration,
HHS.
mstockstill on PROD1PC66 with NOTICES
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
availability of effectiveness and target
animal safety data that may be used in
support of a new animal drug
application (NADA) or supplemental
NADA for use of chloramine-T by
immersion for the control of mortality in
freshwater-reared salmonids due to
bacterial gill disease. The data,
contained in Public Master File (PMF)
5893, were compiled by the U.S.
Department of the Interior, U.S. Fish
and Wildlife Service, Aquatic Animal
Drug Approval Partnership Program.
ADDRESSES: Submit NADAs or
supplemental NADAs to the Document
Control Unit (HFV–199), Center for
Veterinary Medicine, Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855.
FOR FURTHER INFORMATION CONTACT:
Donald A. Prater, Center for Veterinary
Medicine (HFV–130), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 240–276–8343, email: donald.prater@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
Chloramine-T used by immersion for
control of mortality in freshwater-reared
salmonids due to bacterial gill disease is
a new animal drug under section 201(v)
of the Federal Food, Drug, and Cosmetic
Act (the act) (21 U.S.C. 321(v)). As a
new animal drug, chloramine-T is
subject to section 512 of the act (21
U.S.C. 360b) which requires that its uses
be the subject of an approved NADA or
supplemental NADA. Fish are a minor
species under § 514.1(d)(1)(ii) (21 CFR
514.1(d)(1)(ii)).
The U.S. Department of the Interior,
U.S. Fish and Wildlife Service, Aquatic
Animal Drug Approval Partnership
Program, 4050 Bridger Canyon Rd.,
Bozeman, MT 59715, has provided
effectiveness and target animal safety
VerDate Aug<31>2005
17:48 Aug 20, 2008
Jkt 214001
data for use of chloramine-T by
immersion for control of mortality in
freshwater-reared salmonids due to
bacterial gill disease. These data are
contained in PMF 5893.
Sponsors of NADAs or supplemental
NADAs may, without further
authorization, reference the PMF 5893
to support approval of an application
filed under § 514.1(d). An NADA or
supplemental NADA must include, in
addition to reference to the PMF, animal
drug labeling and other information
needed for approval, such as: data
concerning human food safety; and
manufacturing methods, facilities, and
controls. Persons desiring more
information concerning PMF 5893 or
requirements for approval of an NADA
or supplemental NADA may contact the
Center for Veterinary Medicine (see FOR
FURTHER INFORMATION CONTACT).
In accordance with the freedom of
information provisions of 21 CFR part
20, a summary of safety and
effectiveness data provided in PMF
5893 to support approval of an
application may be seen in the Division
of Dockets Management (HFA–305),
Food and Drug Administration, 5630
Fishers Lane, rm. 1061, Rockville, MD
20852, from 9 a.m. to 4 p.m., Monday
through Friday.
Dated: August 8, 2008.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. E8–19299 Filed 8–20–08; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice
is hereby given of the following
meetings.
The meetings 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 material,
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: Center for Scientific
Review Special Emphasis Panel; Shared
Instrumentation (S10) Review.
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49465
Date: September 8, 2008.
Time: 8:30 a.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency O’Hare, 9300 Bryn
Mawr Avenue, Rosemont, IL 60018.
Contact Person: Barbara Whitmarsh, PhD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 2206,
MSC 7890, Bethesda, MD 20892, (301) 435–
4511, whitmarshb@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: Cell Biology
Integrated Review Group Intercellular
Interactions Study Section.
Date: September 22–23, 2008.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: George Washington University Inn,
824 New Hampshire Avenue, NW.,
Washington, DC 20037.
Contact Person: David Balasundaram, PhD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5189,
MSC 7840, Bethesda, MD 20892, 301–435–
1022, balasundaramd@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Applications Related to Dementia, Substance
Abuse, or Behavioral Development.
Date: September 24, 2008.
Time: 2 p.m. to 4 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Ellen K. Schwartz, EDD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3168,
MSC 7770, Bethesda, MD 20892, 301–435–
0681, schwarte@csr.nih.gov.
Name of Committee: Bioengineering
Sciences & Technologies Integrated Review
Group; Biomaterials and Biointerfaces Study
Section.
Date: September 25, 2008.
Time: 8 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: Doubletree Hotel Bethesda, 8120
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Ross D. Shonat, PhD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5156,
MSC 7849, Bethesda, MD 20892, 301–435–
2786, shonatr@csr.nih.gov.
Name of Committee: Bioengineering
Sciences & Technologies Integrated Review
Group; Nanotechnology Study Section.
Date: September 30–October 1, 2008.
Time: 8:30 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hilton Alexandria Old Town, 1767
King Street, Alexandria, VA 22314.
Contact Person: Joseph D. Mosca, PhD,
Scientific Review Officer, Center for
E:\FR\FM\21AUN1.SGM
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]]>Agencies
[Federal Register Volume 73, Number 163 (Thursday, August 21, 2008)]
[Notices]
[Pages 49464-49465]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-19220]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: State Plan for the Temporary Assistance for Needy Families
(TANF).
OMB No.: 0970-0145.
Description: The State plan is a mandatory statement submitted to
the Secretary of the Department of Health and Human Services by the
State. It consists of an outline of how the States TANF program will be
administered and operated and certain required certifications by the
States Chief Executive Officer. Its submittal triggers the States
family assistance grant funding and it is used to provide the public
with information about the program. If a State makes changes in its
program, it must submit a State plan amendment.
Respondents: The 50 States, the District of Columbia, Guam, Puerto
Rico and the Virgin Islands.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Temporary Assistance to Needy Families State 54 0.50 33 891
Plan Guidance..............................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 891.
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-
6974, Attn: Desk Officer for the Administration for Children and
Families.
[[Page 49465]]
Dated: August 14, 2008.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. E8-19220 Filed 8-20-08; 8:45 am]
BILLING CODE 4184-01-M
