83 FR 30735 - Proposed Information Collection Activity

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families

Federal Register Volume 83, Issue 126 (June 29, 2018)

Page Range		30735-30736
FR Document		2018-14037

Federal Register, Volume 83 Issue 126 (Friday, June 29, 2018)

[Federal Register Volume 83, Number 126 (Friday, June 29, 2018)]
[Notices]
[Pages 30735-30736]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2018-14037]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity

AGENCY: Office of Planning, Research, and Evaluation; ACF; HHS.

ACTION: Request for Public Comment.

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TITLE: Temporary Assistance for Needy Families (TANF) Data Innovations 
(TDI) Project (New Collection).
    The Administration for Children and Families (ACF) within the U.S. 
Department of Health and Human Services (HHS) proposes to collect 
information as part of the TANF Data Innovations (TDI) project. TDI is 
an investment to expand the integration, analysis, and use of TANF data 
to improve program administration, payment integrity, and outcomes for 
participants.
    TDI will start by assessing the needs and readiness of TANF 
agencies across the country to set up and operate data systems to 
support program improvement. A key goal of the needs assessment is to 
help categorize states' readiness to effectively use data and produce 
evidence. Informed by this assessment and discussions with key 
stakeholders, TDI will support a broad learning collaborative of state 
agencies and other entities related to the TANF program, including a 
range of Technical Assistance (TA) options to help states improve their 
use of TANF and other program data.
    This information collection request will consist of a needs 
assessment survey to be completed by state TANF agency administrators 
and staff to gather detailed information about their capacities and 
needs. These data will help HHS to better understand the challenges and 
barriers states face in using data and research to inform program 
decision-making, and they will help the TDI team design future 
technical assistance activities for TANF agencies to address states' 
challenges.
    Respondents: State TANF Administrators and TANF agency staff. We 
expect four respondents per state or territory.

[[Page 30736]]



                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                Total/annual      Number of     Average  burden
                 Instrument                      number of      responses  per      hours per     Annual  burden
                                                respondents       respondent        response          hours
----------------------------------------------------------------------------------------------------------------
Needs Assessment Survey.....................             216                2             0.25              108
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 108.

DATES: Comments due within 60 days of publication. 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.

ADDRESSES: 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 Planning, Research, and 
Evaluation, 330 C Street SW, Washington, DC 20201, Attn: OPRE Reports 
Clearance Officer. Email address: [email protected]. All 
requests should be identified by the title of the information 
collection.

SUPPLEMENTARY INFORMATION: 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.

    Authority: Sec. 413, Pub. L. 115-31.

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2018-14037 Filed 6-28-18; 8:45 am]
 BILLING CODE 4184-09-P

30736 Federal Register / Vol. 83, No. 126 / Friday, June 29, 2018 / Notices

ANNUAL BURDEN ESTIMATES
Number of Average
Total/annual Annual
responses burden
Instrument number of burden
per hours per
respondents hours
respondent response

Needs Assessment Survey ............................................................................. 216 2 0.25 108

Estimated Total Annual Burden DEPARTMENT OF HEALTH AND Administrative Practices and
Hours: 108. HUMAN SERVICES Procedures; Formal Evidentiary Public
Hearing
DATES: Comments due within 60 days of
Food and Drug Administration
publication. In compliance with the OMB Control Number 0910–0191—
requirements of Section 3506(c)(2)(A) of Extension
[Docket No. FDA–2014–N–2029]
the Paperwork Reduction Act of 1995, The Administrative Procedures Act (5
the Administration for Children and Agency Information Collection U.S.C. 553(e)) provides that every
Families is soliciting public comment Activities; Submission for Office of Agency shall give an interested person
on the specific aspects of the Management and Budget Review; the right to petition for issuance,
information collection described above. Comment Request; Administrative amendment, or repeal of a rule. Section
Practices and Procedures; Formal 10.30 (21 CFR 10.30) sets forth the
ADDRESSES: Copies of the proposed
format and procedures by which an
collection of information can be Evidentiary Public Hearing
interested person may submit to FDA, in
obtained and comments may be accordance with § 10.20 (21 CFR 10.20),
forwarded by writing to the AGENCY: Food and Drug Administration,
HHS. a citizen petition requesting the
Administration for Children and Commissioner of Food and Drugs (the
Families, Office of Planning, Research, ACTION: Notice. Commissioner) to issue, amend, or
and Evaluation, 330 C Street SW, revoke a regulation or order, or to take
Washington, DC 20201, Attn: OPRE SUMMARY: The Food and Drug or refrain from taking any other form of
Reports Clearance Officer. Email Administration (FDA) is announcing administrative action.
address: OPREinfocollection@ that a proposed collection of The Commissioner may grant or deny
acf.hhs.gov. All requests should be information has been submitted to the such a petition, in whole or in part, and
identified by the title of the information Office of Management and Budget may grant such other relief or take other
collection. (OMB) for review and clearance under action as the petition warrants.
the Paperwork Reduction Act of 1995. Respondents are individuals or
SUPPLEMENTARY INFORMATION: The
households, State or local governments,
Department specifically requests DATES: Fax written comments on the and not-for-profit institutions or groups.
comments on (a) whether the proposed collection of information by July 30, Section 10.33 (21 CFR 10.33), issued
collection of information is necessary 2018. under section 701(a) of the Federal,
for the proper performance of the Food, Drug, and Cosmetic Act (FD&C
functions of the agency, including ADDRESSES: To ensure that comments on Act) (21 U.S.C. 371(a)), sets forth the
whether the information shall have the information collection are received, format and procedures by which an
practical utility; (b) the accuracy of the OMB recommends that written interested person may request
agency’s estimate of the burden of the comments be faxed to the Office of reconsideration of part or all of a
proposed collection of information; (c) Information and Regulatory Affairs, decision of the Commissioner on a
the quality, utility, and clarity of the OMB, Attn: FDA Desk Officer, Fax: 202– petition submitted under 21 CFR 10.25
information to be collected; and (d) 395–7285, or emailed to oira_ (Initiation of administrative
ways to minimize the burden of the submission@omb.eop.gov. All proceedings). A petition for
collection of information on comments should be identified with the reconsideration must contain a full
respondents, including through the use OMB control number 0910–0191. Also statement in a well-organized format of
of automated collection techniques or include the FDA docket number found the factual and legal grounds upon
other forms of information technology. in brackets in the heading of this which the petition relies. The grounds
Consideration will be given to document. must demonstrate that relevant
comments and suggestions submitted information and views contained in the
FOR FURTHER INFORMATION CONTACT: administrative record were not
within 60 days of this publication.
Amber Sanford, Office of Operations, previously or not adequately considered
Authority: Sec. 413, Pub. L. 115–31. Food and Drug Administration, Three by the Commissioner. The respondent
Mary B. Jones, White Flint North, 10A–12M, 11601 must submit a petition no later than 30
Landsdown St., North Bethesda, MD days after the decision involved.
ACF/OPRE Certifying Officer.
20852, 301–796–8867, PRAStaff@ However, the Commissioner may, for
[FR Doc. 2018–14037 Filed 6–28–18; 8:45 am]
good cause, permit a petition to be filed
sradovich on DSK3GMQ082PROD with NOTICES

fda.hhs.gov.
BILLING CODE 4184–09–P after 30 days. An interested person who
SUPPLEMENTARY INFORMATION: In wishes to rely on information or views
compliance with 44 U.S.C. 3507, FDA not included in the administrative
has submitted the following proposed record shall submit them with a new
collection of information to OMB for petition to modify the decision. FDA
review and clearance. uses the information provided in the
request to determine whether to grant

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Document Created: 2018-06-29 01:13:32
Document Modified: 2018-06-29 01:13:32

Category		Regulatory Information
Collection		Federal Register
sudoc Class		AE 2.7: GS 4.107: AE 2.106:
Publisher		Office of the Federal Register, National Archives and Records Administration
Section		Notices
Action		Request for Public Comment.
Dates		Comments due within 60 days of publication. 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.
FR Citation		83 FR 30735

83 FR 30735 - Proposed Information Collection Activity

DEPARTMENT OF HEALTH AND HUMAN SERVICESAdministration for Children and Families

Federal Register Volume 83, Issue 126 (June 29, 2018)

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families