Proposed Information Collection Activity; Comment Request, 5447-5448 [2019-02915]

Download as PDF 5447 Federal Register / Vol. 84, No. 35 / Thursday, February 21, 2019 / Notices must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. The term ‘‘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 publish a 30-day notice in the Federal Register concerning each DATES: Comments on the collection(s) of proposed collection of information, information must be received by the including each proposed extension or OMB desk officer by March 25, 2019. reinstatement of an existing collection ADDRESSES: When commenting on the of information, before submitting the proposed information collections, collection to OMB for approval. To please reference the document identifier comply with this requirement, CMS is or OMB control number. To be assured publishing this notice that summarizes consideration, comments and the following proposed collection(s) of recommendations must be received by information for public comment: the OMB desk officer via one of the 1. Type of Information Collection following transmissions: OMB, Office of Request: Reinstatement without change Information and Regulatory Affairs, of a previously approved collection; Attention: CMS Desk Officer, Fax Title of Information Collection: Number: (202) 395–5806 OR Email: Medicaid State Plan Base Plan Pages; OIRA_submission@omb.eop.gov. Use: State Medicaid agencies complete To obtain copies of a supporting the plan pages while we review the statement and any related forms for the information to determine if the state has proposed collection(s) summarized in met all of the requirements of the this notice, you may make your request provisions the states choose to using one of following: implement. If the requirements are met, 1. Access CMS’ website address at website address at https://www.cms.gov/ we will approve the amendments to the state’s Medicaid plan giving the state Regulations-and-Guidance/Legislation/ the authority to implement the PaperworkReductionActof1995/PRAflexibilities. For a state to receive Listing.html. 1. Email your request, including your Medicaid Title XIX funding, there must address, phone number, OMB number, be an approved Title XIX state plan. and CMS document identifier, to Form Number: CMS–179 (OMB control Paperwork@cms.hhs.gov. number 0938–0193); Frequency: 2. Call the Reports Clearance Office at Occasionally; Affected Public: State, (410) 786–1326. Local, and Tribal Governments; Number FOR FURTHER INFORMATION CONTACT: of Respondents: 56; Total Annual William Parham at (410) 786–4669. Responses: 1,120; Total Annual Hours: 22,400. (For policy questions regarding SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) this collection contact Annette Pearson at 410–786–6958.) (44 U.S.C. 3501–3520), federal agencies persons are invited to send comments regarding the burden estimate or any other aspect of this collection of information, including the necessity and utility of the proposed information collection for the proper performance of the agency’s functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden. Dated: February 15, 2019. William N. Parham, III, Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 2019–02996 Filed 2–20–19; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families [OMB No.: 0970–0379] Proposed Information Collection Activity; Comment Request Title: Project Outcome Assessment Survey. Description: The information collected by the Project Outcome Assessment Survey is needed for two main reasons: (1) To collect crucial information required to report on the Administration for Native Americans’ (ANA) established Government Performance and Results Act (GPRA) measures, and (2) to properly abide by ANA’s congressionally-mandated statute (42 United States Code 2991 et seq.) found within the Native American Programs Act of 1974, as amended, which states that ANA will evaluate projects assisted through ANA grant dollars ‘‘including evaluations that describe and measure the impact of such projects, their effectiveness in achieving stated goals, their impact on related programs, and their structure and mechanisms for delivery of services.’’ The information collected with this survey will fulfill ANA’s statutory requirement and will also serve as an important planning and performance tool for ANA. Respondents: Tribal Governments, Native American nonprofit organizations, and Tribal Colleges and Universities amozie on DSK3GDR082PROD with NOTICES1 ANNUAL BURDEN ESTIMATES Instrument Number of respondents Number of responses per respondent Average burden hours per response Total burden hours ANA Project Outcome Assessment Survey .................................................... 85 1 6 510 Estimated Total Annual Burden Hours: 510. In compliance with the requirements of the Paperwork Reduction Act of 1995 (Pub. L. 104–13, 44 U.S.C. Chap 35), the Administration for Children and Families is soliciting public comment VerDate Sep<11>2014 17:08 Feb 20, 2019 Jkt 247001 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 Planning, Research PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 and Evaluation, 330 C Street SW, Washington DC 20201. Attn: ACF Reports Clearance Officer. Email address: infocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. E:\FR\FM\21FEN1.SGM 21FEN1 5448 Federal Register / Vol. 84, No. 35 / Thursday, February 21, 2019 / 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. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2019–02915 Filed 2–20–19; 8:45 am] BILLING CODE 4184–34–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2014–D–1939] Use of Investigational Tobacco Products; Revised Draft Guidance for Industry and Investigators; Availability; Agency Information Collection Activities; Proposed Collection; Comment Request AGENCY: Food and Drug Administration, HHS. ACTION: Notice of availability. The Food and Drug Administration (FDA) is announcing the availability of a revised draft guidance for industry and investigators entitled ‘‘Use of Investigational Tobacco Products.’’ The revised draft guidance replaces the draft guidance of the same title announced in the Federal Register of September 24, 2015 (September 2015 draft guidance). The revised draft guidance, when finalized, will describe FDA’s current thinking regarding the definition of ‘‘investigational tobacco product’’ and will discuss the kind of information FDA intends to consider in making enforcement decisions regarding the use of investigational tobacco products until regulations governing the use of investigational tobacco products become effective or FDA provides written notice of its intent to change its enforcement policy. DATES: Submit either electronic or written comments on the draft guidance by April 22, 2019 to ensure that the Agency considers your comment on this amozie on DSK3GDR082PROD with NOTICES1 SUMMARY: VerDate Sep<11>2014 17:08 Feb 20, 2019 Jkt 247001 draft guidance before it begins work on the final version of the guidance. Submit electronic or written comments on the proposed collection of information by April 22, 2019. ADDRESSES: You may submit comments on any guidance at any time as follows: Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https:// www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else’s Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on https://www.regulations.gov. • If you want to submit a comment with confidential information that you do not wish to be made available to the public, submit the comment as a written/paper submission and in the manner detailed (see ‘‘Written/Paper Submissions’’ and ‘‘Instructions’’). Written/Paper Submissions Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Dockets Management Staff (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Dockets Management Staff, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ‘‘Instructions.’’ Instructions: All submissions received must include the Docket No. FDA– 2014–D–1939 for ‘‘Use of Investigational Tobacco Products; Revised Draft Guidance for Industry and Investigators; Availability; Agency Information Collection Activities; Proposed Collection; Comment Request.’’ Received comments will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.’’ The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on https://www.regulations.gov. Submit both copies to the Dockets Management Staff. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https://www.gpo.gov/ fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. You may submit comments on any guidance at any time (see 21 CFR 10.115(g)(5)). Submit written requests for single copies of this draft guidance to the Center for Tobacco Products, Food and Drug Administration, Document Control Center, Bldg. 71, Rm. G335, 10903 New Hampshire Ave., Silver Spring, MD 20993–0002. Send one self-addressed adhesive label to assist that office in processing your request or include a fax number to which the draft guidance may be sent. See the SUPPLEMENTARY INFORMATION section for information on electronic access to the draft guidance. FOR FURTHER INFORMATION CONTACT: With regard to the draft guidance: Laura Rich or Samantha LohCollado, E:\FR\FM\21FEN1.SGM 21FEN1

Agencies

[Federal Register Volume 84, Number 35 (Thursday, February 21, 2019)]
[Notices]
[Pages 5447-5448]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-02915]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families

[OMB No.: 0970-0379]


Proposed Information Collection Activity; Comment Request

    Title: Project Outcome Assessment Survey.
    Description: The information collected by the Project Outcome 
Assessment Survey is needed for two main reasons: (1) To collect 
crucial information required to report on the Administration for Native 
Americans' (ANA) established Government Performance and Results Act 
(GPRA) measures, and (2) to properly abide by ANA's congressionally-
mandated statute (42 United States Code 2991 et seq.) found within the 
Native American Programs Act of 1974, as amended, which states that ANA 
will evaluate projects assisted through ANA grant dollars ``including 
evaluations that describe and measure the impact of such projects, 
their effectiveness in achieving stated goals, their impact on related 
programs, and their structure and mechanisms for delivery of 
services.'' The information collected with this survey will fulfill 
ANA's statutory requirement and will also serve as an important 
planning and performance tool for ANA.
    Respondents: Tribal Governments, Native American nonprofit 
organizations, and Tribal Colleges and Universities

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                  Number of     Average  burden
                 Instrument                      Number of      responses  per     hours  per     Total  burden
                                                respondents       respondent        response          hours
----------------------------------------------------------------------------------------------------------------
ANA Project Outcome Assessment Survey.......              85                1                6              510
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 510.
    In compliance with the requirements of the Paperwork Reduction Act 
of 1995 (Pub. L. 104-13, 44 U.S.C. Chap 35), 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 Planning, Research and Evaluation, 330 C Street SW, 
Washington DC 20201. Attn: ACF Reports Clearance Officer. Email 
address: infocollection@acf.hhs.gov. All requests should be identified 
by the title of the information collection.

[[Page 5448]]

    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.

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019-02915 Filed 2-20-19; 8:45 am]
BILLING CODE 4184-34-P