Proposed Information Collection Activity; Comment Request, 32213-32214 [2011-13768]
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Federal Register / Vol. 76, No. 107 / Friday, June 3, 2011 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
PHHS Block Grant Awardees ...................
Work Plan .................................................
Annual Report ..........................................
Dated: May 27, 2011.
Daniel Holcomb,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2011–13762 Filed 6–2–11; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
61
61
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP); Initial Review
Dated: May 25, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2011–13767 Filed 6–2–11; 8:45 am]
The meeting announced below
concerns Human Immunodeficiency
Virus (HIV) Prevention Projects for
Young Men of Color, Funding
Opportunity Announcement (FOA)
PS11–1113, initial review.
Correction: The notice was published
in the Federal Register on February 22,
2011, Volume 76, Number 35, Pages
9785–9786. The place should read as
follows:
Place: Hilton Atlanta Hotel, 255
Courtland Street, NE., Atlanta, Georgia
30303, Telephone: (404) 659–2000.
Contact Person for More Information:
Harriette Lynch, Public Health Analyst,
Extramural Programs, National Center
for HIV, Hepatitis and Sexually
Transmitted Diseases Prevention, CDC,
1600 Clifton Road, NE., Mailstop E–60,
Atlanta, Georgia 30333, Telephone:
(404) 498–2726, e-mail
HLynch@cdc.gov.
Number of
responses per
respondent
Number of
respondents
Respondents
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: State Court Improvement
Program.
OMB No. 0970–0307.
Description
From the funds appropriated for the
Promoting Safe and Stable Families
Program (PSSF), $10 million is reserved
annually for each of three grants to
facilitate the State Court Improvement
Program (CIP) to facilitate court
improvement in the handling of child
abuse and neglect cases.
The Court Improvement Program
(CIP) is composed of three grants, the
Average burden
per response
(in hours)
1
1
20
15
basic, data, and training grants,
governed by two separate Program
Instructions (PIs). The training and data
grants are governed by the ‘‘new grant’’
PI and the basic grant is governed by the
‘‘basic grant’’ PI. Current PIs require
separate applications and program
assessment reports for each grant. Every
State applies for at least two of the
grants annually and most States apply
for all three. As many of the application
requirements are the same for all three
grants, this results in duplicative work
and high degrees of repetition for State
courts applying for more than one CIP
grant.
The purpose of this Program
Instruction is to streamline and simplify
the application and reporting processes
by consolidating the PIs into one single
PI and requiring one single,
consolidated application package and
program assessment report per State
court annually. These revisions will
satisfy statutory programmatic
requirements and reduce both the
number of required responses and
associated total burden hours for State
courts. This new PI also describes
programmatic and fiscal provisions and
reporting requirements for the grants,
specifies the application submittal and
approval procedures for the grants for
fiscal years 2012 through 2015, and
identifies technical resources for use by
State courts during the course of the
grants. The agency uses the information
received to ensure compliance with the
statute and provide training and
technical assistance to the grantees.
Respondents: State Courts.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
jlentini on DSK4TPTVN1PROD with NOTICES
Application .......................................................................................................
Annual Reports ................................................................................................
Estimated Total Annual Burden
Hours: 9,256.
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
VerDate Mar<15>2010
15:49 Jun 02, 2011
Jkt 223001
52
52
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 Administration,
PO 00000
Frm 00079
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1
1
Average
burden hours
per response
92
86
Total burden
hours
4,784
4,472
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
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03JNN1
32214
Federal Register / Vol. 76, No. 107 / Friday, June 3, 2011 / Notices
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. 2011–13768 Filed 6–2–11; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0410]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Premarket
Notification for a New Dietary
Ingredient
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
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
extension 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 procedure by which a manufacturer
or distributor of dietary supplements or
of a new dietary ingredient is to submit
information to FDA upon which it has
based its conclusion that a dietary
supplement containing a new dietary
ingredient will reasonably be expected
to be safe.
DATES: Submit either electronic or
written comments on the collection of
information by August 2, 2011.
ADDRESSES: Submit electronic
comments on the collection of
jlentini on DSK4TPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
15:49 Jun 02, 2011
Jkt 223001
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:
Denver Presley, Jr., Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3793.
SUPPLEMENTARY INFORMATION: 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 extension 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.
Premarket Notification for a New
Dietary Ingredient—21 CFR 190.6
(OMB Control Number 0910–0330)—
Extension
Section 413(a) of the Federal Food,
Drug, and Cosmetic Act (the FD&C Act)
(21 U.S.C. 350b(a)) provides that at least
PO 00000
Frm 00080
Fmt 4703
Sfmt 4703
75 days before the introduction or
delivery for introduction into interstate
commerce of a dietary supplement that
contains a new dietary ingredient, a
manufacturer or distributor of dietary
supplements or of a new dietary
ingredient is to submit to FDA (as
delegate for the Secretary of Health and
Human Services) information upon
which the manufacturer or distributor
has based its conclusion that a dietary
supplement containing a new dietary
ingredient will reasonably be expected
to be safe (part 190 (21 CFR part 190))
implements these statutory provisions.
Section 190.6(a) requires each
manufacturer or distributor of a dietary
supplement containing a new dietary
ingredient, or of a new dietary
ingredient, to submit to the Office of
Nutrition, Labeling, and Dietary
Supplements notification of the basis for
their conclusion that said supplement or
ingredient will reasonably be expected
to be safe. Section 190.6(b) requires that
the notification include the following:
(1) The complete name and address of
the manufacturer or distributor; (2) the
name of the new dietary ingredient; (3)
a description of the dietary supplements
that contain the new dietary ingredient;
and (4) the history of use or other
evidence of safety establishing that the
dietary ingredient will reasonably be
expected to be safe.
The notification requirements
described previously are designed to
enable FDA to monitor the introduction
into the food supply of new dietary
ingredients and dietary supplements
that contain new dietary ingredients, in
order to protect consumers from the
introduction of unsafe dietary
supplements into interstate commerce.
FDA uses the information collected
under these regulations to help ensure
that a manufacturer or distributor of a
dietary supplement containing a new
dietary ingredient is in full compliance
with the FD&C Act.
Description of Respondents: The
respondents to this collection of
information are firms in the dietary
supplement industry, including dietary
supplement and dietary ingredient
manufacturers, packagers and repackagers, holders, labelers and relabelers, distributors, warehouses,
exporters, and importers.
FDA estimates the burden of this
collection of information as follows:
E:\FR\FM\03JNN1.SGM
03JNN1
]]>Agencies
[Federal Register Volume 76, Number 107 (Friday, June 3, 2011)]
[Notices]
[Pages 32213-32214]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-13768]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Title: State Court Improvement Program.
OMB No. 0970-0307.
Description
From the funds appropriated for the Promoting Safe and Stable
Families Program (PSSF), $10 million is reserved annually for each of
three grants to facilitate the State Court Improvement Program (CIP) to
facilitate court improvement in the handling of child abuse and neglect
cases.
The Court Improvement Program (CIP) is composed of three grants,
the basic, data, and training grants, governed by two separate Program
Instructions (PIs). The training and data grants are governed by the
``new grant'' PI and the basic grant is governed by the ``basic grant''
PI. Current PIs require separate applications and program assessment
reports for each grant. Every State applies for at least two of the
grants annually and most States apply for all three. As many of the
application requirements are the same for all three grants, this
results in duplicative work and high degrees of repetition for State
courts applying for more than one CIP grant.
The purpose of this Program Instruction is to streamline and
simplify the application and reporting processes by consolidating the
PIs into one single PI and requiring one single, consolidated
application package and program assessment report per State court
annually. These revisions will satisfy statutory programmatic
requirements and reduce both the number of required responses and
associated total burden hours for State courts. This new PI also
describes programmatic and fiscal provisions and reporting requirements
for the grants, specifies the application submittal and approval
procedures for the grants for fiscal years 2012 through 2015, and
identifies technical resources for use by State courts during the
course of the grants. The agency uses the information received to
ensure compliance with the statute and provide training and technical
assistance to the grantees.
Respondents: State Courts.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average
Instrument Number of responses per burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
Application..................................... 52 1 92 4,784
Annual Reports.................................. 52 1 86 4,472
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 9,256.
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
Administration, Office of Information Services, 370 L'Enfant Promenade,
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail
address: infocollection@acf.hhs.gov. All requests should be identified
by the title of the information collection.
[[Page 32214]]
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. 2011-13768 Filed 6-2-11; 8:45 am]
BILLING CODE 4184-01-P
