National Institute of Arthritis and Musculoskeletal and Skin Diseases; Notice of Closed Meetings, 70679-70680 [2010-29091]
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70679
Federal Register / Vol. 75, No. 222 / Thursday, November 18, 2010 / Notices
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN—Continued
Number of
respondents
Data collection method
Total burden
hours
Average hourly
wage rate*
Total cost burden
Focus Groups ..................................................................................
Key Informant Interviews .................................................................
99
30
149
30
33.51
33.51
4,993
1,005
Total ..........................................................................................
40,349
5542
NA
185,712
* Based upon the mean of the average wages for healthcare practitioner and technical occupations (29–0000) presented in the National Compensation Survey: Occupational wages in the United States, May 2009, U.S. Department of Labor, Bureau of Labor Statistics.
Estimated Annual Costs to the Federal
Government
and 30 key informant interviews and to
analyze and present their results. This
amount is the contract total for AFYA’s
contract with AHRQ to evaluate the
NGC. This amount, includes the costs
for project development and
management ($70,000 or 20% of the
entire contract amount); data collection
Exhibit 3 shows the estimated total
and annualized cost to the government
for this one year project. The total cost
is estimated to be $350,000 to conduct
the one-time survey, 11 focus groups,
activities ($105,000 or 30% of the entire
contract amount); data processing and
analysis ($70,000 or 20% of the entire
contract amount); and administrative
support activities and reporting
($105,000 or 30% of the entire contract
amount).
EXHIBIT 3—ESTIMATED TOTAL AND ANNUALIZED COST
Cost component
Total cost
Annualized cost
$70,000
105,000
70,000
105,000
$70,000
105,000
70,000
105,000
Total ..........................................................................................................................................................
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Project Development and Management ..........................................................................................................
Data Collection Activities .................................................................................................................................
Data Processing and Analysis .........................................................................................................................
Administrative Support and Reporting .............................................................................................................
350,000
350,000
Request for Comments
In accordance with the above-cited
Paperwork Reduction Act legislation,
comments on AHRQs 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 healthcare research and
healthcare 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: November 10, 2010.
Carolyn M. Clancy,
Director.
[FR Doc. 2010–29010 Filed 11–17–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0554]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approval;
Manufactured Food Regulatory
Program Standards
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a collection of information entitled
‘‘Manufactured Food Regulatory
Program Standards’’ has been approved
by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Daniel Gittleson, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
5156, Daniel.Gittleson@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In the
Federal Register of March 3, 2010 (75
FR 9605), the agency announced that
the proposed information collection had
been submitted to OMB for review and
clearance under 44 U.S.C. 3507. An
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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 0910–0601. The
approval expires on September 30,
2013. A copy of the supporting
statement for this information collection
is available on the Internet at https://
www.reginfo.gov/public/do/PRAMain.
Dated: November 12, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–29055 Filed 11–17–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Arthritis and
Musculoskeletal and Skin Diseases;
Notice of Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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.,
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70680
Federal Register / Vol. 75, No. 222 / Thursday, November 18, 2010 / Notices
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: National Institute of
Arthritis and Musculoskeletal and Skin
Diseases Special Emphasis Panel, Clinical
Trials Review.
Date: December 2, 2010.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: Courtyard by Marriott, 5520
Wisconsin Avenue, Chevy Chase, MD 20815.
Contact Person: Charles H Washabaugh,
Scientific Review Officer, Scientific Review
Branch, National Institute of Arthritis,
Musculoskeletal and Skin Diseases, National
Institutes of Health, 6701 Democracy Blvd,
Room 824, MSC 4872, Bethesda, MD 20817.
301–594–4952. washabac@mail.nih.gov.
Name of Committee: National Institute of
Arthritis and Musculoskeletal and Skin
Diseases Special Emphasis Panel, Small
Grants Research Review.
Date: December 8, 2010.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, One
Democracy Plaza, 6701 Democracy
Boulevard, Bethesda, MD 20892. (Virtual
Meeting.)
Contact Person: Eric H. Brown, Scientific
Review Officer, Scientific Review Branch,
National Institute of Arthritis,
Musculoskeletal and Skin Diseases, National
Institutes of Health, 6701 Democracy Blvd,
Room 824, MSC 4872, Bethesda, MD 20817.
(301) 594–4955. browneri@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.846, Arthritis,
Musculoskeletal and Skin Diseases Research,
National Institutes of Health, HHS)
Dated: November 10, 2010.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2010–29091 Filed 11–17–10; 8:45 am]
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DEPARTMENT OF HOMELAND
SECURITY
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U.S. Customs and Border Protection
Agency Information Collection
Activities: Request for Information
U.S. Customs and Border
Protection, Department of Homeland
Security.
ACTION: 60-Day Notice and request for
comments; Extension of an existing
collection of information: 1651–0023.
AGENCY:
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As part of its continuing effort
to reduce paperwork and respondent
burden, CBP invites the general public
and other Federal agencies to comment
on an information collection
requirement concerning: Request for
Information (CBP Form 28). This request
for comment is being made pursuant to
the Paperwork Reduction Act of 1995
(Pub. L. 104–13; 44 U.S.C. 3505(c)(2)).
DATES: Written comments should be
received on or before January 18, 2011,
to be assured of consideration.
ADDRESSES: Direct all written comments
to U.S. Customs and Border Protection,
Attn: Tracey Denning, Regulations and
Rulings, Office of International Trade,
799 9th Street, NW., 5th Floor,
Washington, DC 20229–1177.
FOR FURTHER INFORMATION CONTACT:
Requests for additional information
should be directed to Tracey Denning,
U.S. Customs and Border Protection,
Regulations and Rulings, Office of
International Trade, 799 9th Street,
NW., 5th Floor, Washington, DC 20229–
1177, at 202–325–0265.
SUPPLEMENTARY INFORMATION: CBP
invites the general public and other
Federal agencies to comment on
proposed and/or continuing information
collections pursuant to the Paperwork
Reduction Act of 1995 (Pub. L. 104–13;
44 U.S.C. 3505(c)(2)). The comments
should address: (a) Whether the
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimates of the burden of the
collection of information; (c) ways to
enhance the quality, utility, and clarity
of the information to be collected; (d)
ways to minimize the burden including
the use of automated collection
techniques or the use of other forms of
information technology; and (e) the
annual costs burden to respondents or
record keepers from the collection of
information (a total capital/startup costs
and operations and maintenance costs).
The comments that are submitted will
be summarized and included in the CBP
request for Office of Management and
Budget (OMB) approval. All comments
will become a matter of public record.
In this document CBP is soliciting
comments concerning the following
information collection:
Title: Request for Information.
OMB Number: 1651–0023.
Form Number: CBP Form 28.
Abstract: Under 19 U.S.C. 1500 and
1401a, Customs and Border Protection
(CBP) is responsible for appraising
imported merchandise by ascertaining
its value, classifying merchandise under
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the tariff schedule, and assessing a rate
and amount of duty to be paid. On
occasions when the invoice or other
documentation does not provide
sufficient information for appraisement
or classification, the CBP Officer
requests additional information through
the use of CBP Form 28, ‘‘Request for
Information’’. This form is completed by
CBP personnel requesting additional
information and the importers, or their
agents, respond in the format of their
choice. CBP Form 28 is provided for by
19 CFR 151.11. A copy of this form and
instructions are available at https://
forms.cbp.gov/pdf/CBP_Form_28.pdf.
Current Actions: This submission is
being made to extend the expiration
date with no change to the burden hours
or to CBP Form 28.
Type of Review: Extension (without
change).
Affected Public: Businesses.
Estimated Number of Respondents:
60,000.
Estimated Time per Respondent: 1
hour.
Estimated Total Annual Burden
Hours: 60,000.
Dated: November 15, 2010.
Tracey Denning,
Agency Clearance Officer, U.S. Customs and
Border Protection.
[FR Doc. 2010–29085 Filed 11–17–10; 8:45 am]
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NATIONAL INDIAN GAMING
COMMISSION
Notice of Inquiry and Request for
Information; Notice of Consultation
National Indian Gaming
Commission.
ACTION: Notice of inquiry; notice of
Tribal consultations.
AGENCY:
Authority: 25 U.S.C. 2706(b)(10); E.O.
13175.
This Notice of Inquiry and
Notice of Consultation advises the
public that the National Indian Gaming
Commission (NIGC) is conducting a
comprehensive review of all regulations
promulgated to implement the Indian
Gaming Regulatory Act (IGRA), 25
U.S.C. 2701 et seq. The Commission is
taking a fresh look at its rules in order
to determine whether amendments are
necessary to more effectively implement
IGRA’s policies of protecting Indian
gaming as a means of generating Tribal
revenue, ensuring that gaming is
conducted fairly and honestly by both
the operator and players, and ensuring
that Tribes are the primary beneficiaries
of gaming operations. The Commission’s
SUMMARY:
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Agencies
[Federal Register Volume 75, Number 222 (Thursday, November 18, 2010)]
[Notices]
[Pages 70679-70680]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-29091]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Institute of Arthritis and Musculoskeletal and Skin
Diseases; Notice of Closed Meetings
Pursuant to section 10(d) of the Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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.,
[[Page 70680]]
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: National Institute of Arthritis and
Musculoskeletal and Skin Diseases Special Emphasis Panel, Clinical
Trials Review.
Date: December 2, 2010.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant applications.
Place: Courtyard by Marriott, 5520 Wisconsin Avenue, Chevy
Chase, MD 20815.
Contact Person: Charles H Washabaugh, Scientific Review Officer,
Scientific Review Branch, National Institute of Arthritis,
Musculoskeletal and Skin Diseases, National Institutes of Health,
6701 Democracy Blvd, Room 824, MSC 4872, Bethesda, MD 20817. 301-
594-4952. washabac@mail.nih.gov.
Name of Committee: National Institute of Arthritis and
Musculoskeletal and Skin Diseases Special Emphasis Panel, Small
Grants Research Review.
Date: December 8, 2010.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant applications.
Place: National Institutes of Health, One Democracy Plaza, 6701
Democracy Boulevard, Bethesda, MD 20892. (Virtual Meeting.)
Contact Person: Eric H. Brown, Scientific Review Officer,
Scientific Review Branch, National Institute of Arthritis,
Musculoskeletal and Skin Diseases, National Institutes of Health,
6701 Democracy Blvd, Room 824, MSC 4872, Bethesda, MD 20817. (301)
594-4955. browneri@mail.nih.gov.
(Catalogue of Federal Domestic Assistance Program Nos. 93.846,
Arthritis, Musculoskeletal and Skin Diseases Research, National
Institutes of Health, HHS)
Dated: November 10, 2010.
Jennifer S. Spaeth,
Director, Office of Federal Advisory Committee Policy.
[FR Doc. 2010-29091 Filed 11-17-10; 8:45 am]
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