Proposed Information Collection Activity; Comment Request, 13610-13611 [2012-5421]
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13610
Federal Register / Vol. 77, No. 45 / Wednesday, March 7, 2012 / Notices
Estimated Total Annual Burden
Hours: 96,000.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comments
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, 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.
The Department specifically requests
comments on: (a) Whether the proposed
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 estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2012–5501 Filed 3–6–12; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
OMB No.: 0980–0242.
Description: Section 646 of the Head
Start Act requires the Secretary to
prescribe a timeline for conducting
administrative hearings when adverse
actions are taken or proposed against
Head Start or Early Head Start grantees
or delegate agencies. The Office of Head
Start is proposing to renew without
changes this rule which implements
these requirements and which prescribe
when a grantee must submit information
and what that information should
include to support a contention that
adverse action should not be taken.
Respondents: Head Start and Early
Head Start grantees and delegate
agencies against which the Head Start
Bureau has taken or proposes to take
adverse actions.
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Appeal Procedures for Head
Start Grantees and Current or
Prospective Delegate Agencies.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Number of
responses
per
respondent
Average
burden
hours per
response
Total
burden
hours
Adverse Action .................................................................................................
srobinson on DSK4SPTVN1PROD with NOTICES
Instrument
20
1
26
520
Estimated Total Annual Burden
Hours: 520.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, 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.
The Department specifically requests
comments on: (a) Whether the proposed
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 estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
VerDate Mar<15>2010
18:40 Mar 06, 2012
Jkt 226001
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Bob Sargis,
Reports Clearance Officer.
[FR Doc. 2012–5499 Filed 3–6–12; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Project
OMB No.: 0970–0193.
Description: The Head Start Bureau is
proposing to renew, without changes,
the information collections activities for
the regulations in 45 CFR part 1309. The
part contains the administrative
requirements applicable to Head Start
and Early Head Start grantees, when
applying for funding to purchase,
renovate or construct Head Start
program facilities. The regulations
ensure that standard business practices
are applied when acquiring real
property and that federal interest is
preserved in properties acquired with
public funds. The regulations further
ensure compliance with all other federal
statues applicable to the expenditure of
federal funds when acquiring real
property.
Respondents: Head Start and Early
Head Start programs are delegate
agencies.
Title: Head Start Facilities
Construction, Purchase and Major
Renovations.
PO 00000
Frm 00082
Fmt 4703
Sfmt 4703
E:\FR\FM\07MRN1.SGM
07MRN1
13611
Federal Register / Vol. 77, No. 45 / Wednesday, March 7, 2012 / Notices
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average burden hours per
respondent
Total burden
hours
Administrative Requirements ...........................................................................
200
1
41
8,200
Estimated Total Annual Burden
Hours: 8,200.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comments
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, 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.
The Department specifically requests
comments on: (a) Whether the proposed
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 estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Bob Sargis,
Reports Clearance Officer.
[FR Doc. 2012–5421 Filed 3–6–12; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
srobinson on DSK4SPTVN1PROD with NOTICES
[Docket No. FDA–2012–N–0001]
Arthritis Advisory Committee; Notice
of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
VerDate Mar<15>2010
18:40 Mar 06, 2012
Jkt 226001
(FDA). The meeting will be open to the
public.
Name of Committee: Arthritis
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the Agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on May 8, 2012, from 8:30 a.m. to
5 p.m.
Location: FDA White Oak Campus,
10903 New Hampshire Ave., Building
31 Conference Center, the Great Room
(rm. 1503), Silver Spring, MD 20993–
0002. Information regarding special
accommodations due to a disability,
visitor parking, and transportation may
be accessed at: https://www.fda.gov/
AdvisoryCommittees/default.htm; under
the heading ‘‘Resources for You,’’ click
on ‘‘Public Meetings at the FDA White
Oak Campus.’’ Please note that visitors
to the White Oak Campus must enter
through Building 1.
Contact Person: Philip Bautista,
Center for Drug Evaluation and
Research, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 31, rm. 2417, Silver Spring,
MD 20993–0002, 301–796–9001, FAX:
301–847–8533, email: AAC@fda.gov, or
FDA Advisory Committee Information
Line, 1–800–741–8138 (301–443–0572
in the Washington, DC area), and follow
the prompts to the desired center or
product area. Please call the Information
Line for up-to-date information on this
meeting. A notice in the Federal
Register about last minute modifications
that impact a previously announced
advisory committee meeting cannot
always be published quickly enough to
provide timely notice. Therefore, you
should always check the Agency’s Web
site and call the appropriate advisory
committee hot line/phone line to learn
about possible modifications before
coming to the meeting.
Agenda: The committee will discuss
supplemental biologics license
application 125249, ARCALYST
(rilonacept) injection, Regeneron
Pharmaceuticals, Inc., for the following
proposed indication: ‘‘ARCALYST
(rilonacept) is an interleukin-1 blocker
indicated for the prevention of gout
flares during initiation of uric-acid
lowering therapy in adult patients with
gout. ARCALYST has not been studied
PO 00000
Frm 00083
Fmt 4703
Sfmt 4703
for longer than 16 weeks in this clinical
setting.’’
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
available at https://www.fda.gov/
AdvisoryCommittees/Calendar/
default.htm. Scroll down to the
appropriate advisory committee link.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person on or before April 24, 2012. Oral
presentations from the public will be
scheduled between approximately 1
p.m. and 2 p.m. Those individuals
interested in making formal oral
presentations should notify the contact
person and submit a brief statement of
the general nature of the evidence or
arguments they wish to present, the
names and addresses of proposed
participants, and an indication of the
approximate time requested to make
their presentation on or before April 16,
2012. Time allotted for each
presentation may be limited. If the
number of registrants requesting to
speak is greater than can be reasonably
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by April 17, 2012.
Persons attending FDA’s advisory
committee meetings are advised that the
Agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
a disability, please contact Philip
Bautista at least 7 days in advance of the
meeting.
E:\FR\FM\07MRN1.SGM
07MRN1
Agencies
[Federal Register Volume 77, Number 45 (Wednesday, March 7, 2012)]
[Notices]
[Pages 13610-13611]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-5421]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Project
Title: Head Start Facilities Construction, Purchase and Major
Renovations.
OMB No.: 0970-0193.
Description: The Head Start Bureau is proposing to renew, without
changes, the information collections activities for the regulations in
45 CFR part 1309. The part contains the administrative requirements
applicable to Head Start and Early Head Start grantees, when applying
for funding to purchase, renovate or construct Head Start program
facilities. The regulations ensure that standard business practices are
applied when acquiring real property and that federal interest is
preserved in properties acquired with public funds. The regulations
further ensure compliance with all other federal statues applicable to
the expenditure of federal funds when acquiring real property.
Respondents: Head Start and Early Head Start programs are delegate
agencies.
[[Page 13611]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent respondent hours
----------------------------------------------------------------------------------------------------------------
Administrative Requirements................. 200 1 41 8,200
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 8,200.
In compliance with the requirements of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comments on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, 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.
The Department specifically requests comments on: (a) Whether the
proposed 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 estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Bob Sargis,
Reports Clearance Officer.
[FR Doc. 2012-5421 Filed 3-6-12; 8:45 am]
BILLING CODE 4184-01-P