Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Manufactured Food Regulatory Program Standards, 70679 [2010-29055]
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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 ..........................................................................................................................................................
mstockstill on DSKH9S0YB1PROD with NOTICES
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
SUMMARY:
PO 00000
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Fmt 4703
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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.,
E:\FR\FM\18NON1.SGM
18NON1
]]>Agencies
[Federal Register Volume 75, Number 222 (Thursday, November 18, 2010)]
[Notices]
[Page 70679]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-29055]
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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.
-----------------------------------------------------------------------
SUMMARY: 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 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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