Proposed Information Collection Activity; Comment Request, 32213-32214 [2011-13768]

Download as PDF 32213 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. E:\FR\FM\03JNN1.SGM 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 http:// 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]


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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