Agency Recordkeeping/Reporting Requirements Under Emergency Review by the Office of Management and Budget, 31447-31448 [2010-13106]
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31447
Federal Register / Vol. 75, No. 106 / Thursday, June 3, 2010 / Notices
EXHIBIT 1. ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of respondents
Data collection
Number of responses per
respondent
Hours per response
15
n/a
n/a
Total ..........................................................................................................
Total burden
hours
68
* Individuals
that cannot attend the focus groups will be interviewed one-on-one. Clinical staff includes IC leaders, QI team members and unit
staff. Managers include the chief nursing officer and chief medical officer.
EXHIBIT 2. ESTIMATED ANNUALIZED COST BURDEN
Number of respondents
Data collection
Total burden
hours
Average hourly wage rate
Total cost burden
Pre-intervention focus groups with clinical staff * ............................................
Pre-intervention focus groups with managers * ...............................................
Clinical staff survey ..........................................................................................
3
3
3
27
3
8
$36.73 *
$138.38 **
$36.73 *
$992
$415
$294
Post-intervention focus groups with clinical staff * ...........................................
Post-intervention focus groups with managers * ..............................................
3
3
27
3
$36.73 *
$138.38 **
$992
$415
Total ..........................................................................................................
15
68
na
$3,108
* Based
upon the mean hourly wage for Registered Nurses in Nassau and Suffolk County, NY as reported by the Bureau of Labor Statistics in
May 2008.
** Based on report of a private survey of HR departments conducted in November 2009 in New York, NY published by https://www.saIary.com; 3
chief nursing officers at $101.14/hr and 3 chief medical officers at $175.61/hour.
Estimated Annual Costs to the Federal
Government
Exhibit 3 shows the annualized and
total cost to the federal government for
this two year research project. Project
development covers steps taken to
revise the research plan and begin
implementation. The total cost is
estimated to be $500,001.
EXHIBIT 3. ANNUALIZED AND TOTAL COST TO THE FEDERAL GOVERNMENT
Annualized
cost
Cost component
Total cost
Project Management ................................................................................................................................................
Project Development ...............................................................................................................................................
Data Collection Activities .........................................................................................................................................
Travel .......................................................................................................................................................................
Overhead .................................................................................................................................................................
$125,526
$54,622
$41,864
$4,000
$23,754
$251,052
$109,244
$83,728
$8,000
$47,507
Total ..................................................................................................................................................................
$250,001
$500,001
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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 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
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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
will become a matter of public record.
Dated: May 21, 2010.
Carolyn M. Clancy,
Director.
[FR Doc. 2010–13107 Filed 6–2–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Agency Recordkeeping/Reporting
Requirements Under Emergency
Review by the Office of Management
and Budget
Title: State Personal Responsibility
Education Program.
OMB No.: New Collection.
Description: An emergency request is
being made to solicit comments from
the public on paperwork reduction as it
relates to ACYF’s receipt of the
following documents from applicants
and awardees:
• Application for Formula Grant
• Performance Progress Reports
• Year 1 Implementation Plan
• Performance Measure Reporting
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31448
Federal Register / Vol. 75, No. 106 / Thursday, June 3, 2010 / Notices
Respondents: 50 States and 9
Territories, to include, District of
Columbia, Puerto Rico, Virgin Islands,
Guam, American Samoa, Northern
Mariana Islands, the Federated States of
Micronesia, the Marshall Islands and
Palau
ANNUAL BURDEN ESTIMATES
Number of respondents
Instrument
Number of responses per
respondent
Average burden hours per
response
59
59
59
59
1
2
1
1
40
10
30
10
Application to include program narrative .........................................................
Performance Progress Reports .......................................................................
Year 1 Implementation Plan ............................................................................
Performance Measure Reporting ....................................................................
Estimated Total Annual Burden
Hours: 5900.
Additional Information:
The Year 1 Implementation Plan is
only required to be completed and
submitted in the first year of the project
period. This is a one time submission
and will not occur annually.
The potential awardees could include
organizations and other entities
awarded in year 3 of the project period
in States that did not apply for funding
in the first 2 years of the project period.
A copy of this information collection,
with applicable supporting
documentation, may be obtained by
calling the Administration for Children
and Families, Reports Clearance Officer,
Robert Sargis at (202) 690–7275.
Interested persons are invited to submit
comments regarding this request.
Comments must be received within
thirty days from the publication date of
this Notice.
Comments about the information
collection described above should be
directed to the Office of Information and
Regulatory Affairs, Attn: OMB Desk
Officer for ACF, Office of Management
and Budget, Paperwork Reduction
Project, 725 17th Street NW.,
Washington, DC 20503; FAX: (202) 395–
7285; e-mail:
oira_submission@omb.eop.gov.
Dated: May 25, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–13106 Filed 6–2–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0248]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Format and
Content Requirements for Over-theCounter Drug Product Labeling
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
reinstatement of an existing collection
of information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
the standardized format and content
requirements for the labeling of overthe-counter (OTC) drug products.
DATES: Submit either electronic or
written comments on the collection of
information by August 2, 2010.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Elizabeth Berbakos, Office of
Information Management, Food and
Drug Administration, 1350 Piccard Dr.,
PI50–400B, Rockville, MD 20850, 301–
PO 00000
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Total burden
hours
2360
1180
1770
590
796–3792,
Elizabeth.berbakos@fda.hhs.gov.
Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined in
44 U.S.C. 3502(3) and 5 CFR 1320.3(c)
and includes agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires Federal agencies
to provide a 60-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed reinstatement
of an existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the 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 the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
SUPPLEMENTARY INFORMATION:
Format and Content Requirements for
OTC Drug Product Labeling (OMB
Control Number 0910 0340)—
Reinstatement
In the Federal Register of March 17,
1999 (64 FR 13254), we amended our
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[Federal Register Volume 75, Number 106 (Thursday, June 3, 2010)]
[Notices]
[Pages 31447-31448]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-13106]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Agency Recordkeeping/Reporting Requirements Under Emergency
Review by the Office of Management and Budget
Title: State Personal Responsibility Education Program.
OMB No.: New Collection.
Description: An emergency request is being made to solicit comments
from the public on paperwork reduction as it relates to ACYF's receipt
of the following documents from applicants and awardees:
Application for Formula Grant
Performance Progress Reports
Year 1 Implementation Plan
Performance Measure Reporting
[[Page 31448]]
Respondents: 50 States and 9 Territories, to include, District of
Columbia, Puerto Rico, Virgin Islands, Guam, American Samoa, Northern
Mariana Islands, the Federated States of Micronesia, the Marshall
Islands and Palau
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Application to include program narrative........ 59 1 40 2360
Performance Progress Reports.................... 59 2 10 1180
Year 1 Implementation Plan...................... 59 1 30 1770
Performance Measure Reporting................... 59 1 10 590
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 5900.
Additional Information:
The Year 1 Implementation Plan is only required to be completed and
submitted in the first year of the project period. This is a one time
submission and will not occur annually.
The potential awardees could include organizations and other
entities awarded in year 3 of the project period in States that did not
apply for funding in the first 2 years of the project period.
A copy of this information collection, with applicable supporting
documentation, may be obtained by calling the Administration for
Children and Families, Reports Clearance Officer, Robert Sargis at
(202) 690-7275. Interested persons are invited to submit comments
regarding this request. Comments must be received within thirty days
from the publication date of this Notice.
Comments about the information collection described above should be
directed to the Office of Information and Regulatory Affairs, Attn: OMB
Desk Officer for ACF, Office of Management and Budget, Paperwork
Reduction Project, 725 17th Street NW., Washington, DC 20503; FAX:
(202) 395-7285; e-mail: oira_submission@omb.eop.gov.
Dated: May 25, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010-13106 Filed 6-2-10; 8:45 am]
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