Agency Information Collection Activities: Submission for OMB Review; Comment Request; Alzheimer's and Dementia Program Data Reporting Tool (ADP-DRT) (Previously Entitled: Alzheimer's Disease Supportive Services Program Data Reporting Tool (ADSSP-DRT) and Alzheimer's disease Initiative- Specialized Supportive Services (ADI- SSS) project)), 96002-96003 [2016-31528]

Download as PDF 96002 Federal Register / Vol. 81, No. 250 / Thursday, December 29, 2016 / Notices emailed to them from the CPSTF@ cdc.gov mailbox. asabaliauskas on DSK3SPTVN1PROD with NOTICES FOR FURTHER INFORMATION AND TO RSVP CONTACT: Onslow Smith, The Community Guide Branch; Division of Public Health Information Dissemination; Center for Surveillance, Epidemiology and Laboratory Services; Office of Public Health Scientific Services; Centers for Disease Control and Prevention, 1600 Clifton Road, MS– E–69, Atlanta, GA 30333, phone: (404)498–6778, email: CPSTF@cdc.gov. SUPPLEMENTARY INFORMATION: Purpose: The purpose of the meeting is for the Task Force to consider systematic reviews and issue findings and recommendations based on the reviews. Task Force recommendations provide information about evidencebased options that decision makers and stakeholders can consider when they are determining what best meets the specific needs, preferences, available resources, and constraints of their jurisdictions and constituents. Matters proposed to be discussed: * Cardiovascular disease prevention and control (effectiveness of digital interventions for blood pressure control, mobile phone text messaging for medication adherence), diabetes prevention and control (effectiveness and economic reviews of community health workers for diabetes management, low health literacy sensitive self-management programs for diabetes), health equity promotion (detracking, modified school time), and older adult health (self-management support programs for activities of daily living of older adults). *Pending final approval of review preparations. Roybal Campus Security Guidelines: The Edward R. Roybal Campus is the headquarters of the U.S. Centers for Disease Control and Prevention and is located at 1600 Clifton Road NE., Atlanta, Georgia. The meeting is being held in a Federal government building; therefore, Federal security measures are applicable. All meeting attendees must RSVP by the dates outlined under Meeting Accessibility. In planning your arrival time, please take into account the need to park and clear security. All visitors must enter the Edward R. Roybal Campus through the front entrance on Clifton Road. Vehicles may be searched, and the guard force will then direct visitors to the designated parking area. Upon arrival at the facility, visitors must present government-issued photo identification (e.g., a valid federal identification badge, state driver’s license, state non-driver’s identification VerDate Sep<11>2014 18:41 Dec 28, 2016 Jkt 241001 card, or passport). Non-United States citizens must complete the required security paperwork prior to the meeting date and must present a valid passport, visa, Permanent Resident Card, or other type of work authorization document upon arrival at the facility. All persons entering the building must pass through a metal detector. Visitors will be issued a visitor’s ID badge at the entrance to Building 19 and may be escorted to the meeting room. All items brought to HHS/CDC are subject to inspection. Dated: December 22, 2016. Lauren Hoffmann, Acting Executive Secretary, Centers for Disease Control and Prevention. [FR Doc. 2016–31468 Filed 12–28–16; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Community Living Agency Information Collection Activities: Submission for OMB Review; Comment Request; Alzheimer’s and Dementia Program Data Reporting Tool (ADP–DRT) (Previously Entitled: Alzheimer’s Disease Supportive Services Program Data Reporting Tool (ADSSP–DRT) and Alzheimer’s disease Initiative— Specialized Supportive Services (ADI– SSS) project)) Administration for Community Living, HHS. ACTION: Notice. AGENCY: In compliance with 44 U.S.C. 3507, the Administration on Aging (AoA), Administration for Community Living (ACL), is announcing that the proposed collection of information listed above has been submitted to the Office of Management and Budget (OMB) for review and clearance as required under the Paperwork Reduction Act of 1995. This notice collects comments on the information collection requirements relating to the continuation of an existing data collection for the Alzheimer’s and Dementia Program Data Reporting Tool (ADP–PDR) and expansion of this collection to incorporate ACL grantees of the Alzheimer’s Disease Initiative— Specialized Supportive Services (ADI– SSS) project. DATES: Submit written comments on the collection of information by January 30, 2017. ADDRESSES: Submit written comments on the collection of information by fax to (202) 395–5806 or by email to OIRA_ SUMMARY: PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 submission@omb.eop.gov, Attn: OMB Desk Officer for ACL. FOR FURTHER INFORMATION CONTACT: Erin Long, (202) 795–7389; Erin.Long@ acl.hhs.gov. SUPPLEMENTARY INFORMATION: The Alzheimer’s Disease Supportive Services Program (ADSSP) is authorized through Sections 398, 399 and 399A of the Public Health Service (PHS) Act, as amended by Public Law 101–557, the Home Health Care and Alzheimer’s disease Amendments of 1990. The ADSSP helps state efforts to expand the availability of community-level supportive services for persons with Alzheimer’s disease and their caregivers, including underserved populations. ADI–SSS projects are financed solely by Prevention and Public Health Funds. Similar in scope to ADSSP, ADI–SSS projects are designed to fill gaps in dementia-capable home and community based services (HCBS) for persons living with or those at high risk of developing Alzheimer’s disease and related dementias (ADRD) and their caregivers by providing quality, personcentered services that help them remain independent and safe in their communities. In compliance with the PHS Act, ACL revised the ADSSP Data Reporting Tool (ADSSP–DRT) in 2013 to add demographic data, information on the individuals trained, and service and expenditure data. The 2016 revised Alzheimer’s and Dementia Program Data Reporting Tool (ADP–DRT) retains these changes and has been expanded to collect information about the delivery of direct services by both ADSSP and ADI– SSS grantees, as well as basic demographic information about service recipients. Comments in Response to the 60-Day Federal Register Notice: A 60-day Federal Register Notice was published in the Federal Register on August 23, 2016, Vol. 18, No. 136; pp. 57591. There was one public comment received pertaining to the categories for living arrangements. The comment suggested that the categories needed to have a clear definition. ACL accepted the comment, and the tool was revised by condensing the categories and providing an update to its definition of categories for living arrangements. The proposed ADP–DRT can be found on AoA’s Web site at: https://nadrc.acl.gov/ sites/default/files/uploads/docs/ Proposed%20ADP– DRT%20Update%2011_30_2016.xlsx. Annual Burden Estimates: The estimated hourly burden for this revised ADP–DRT is based on the number of persons served in the most recent ADSSP and ADI grantee data E:\FR\FM\29DEN1.SGM 29DEN1 96003 Federal Register / Vol. 81, No. 250 / Thursday, December 29, 2016 / Notices submission. In addition, the burden hours per response were determined based on reports from a sample of ADSSP and ADI grants. Number of respondents Instrument Type of respondent ADP–DRT ......................................... ADP–DRT ......................................... Local Program Site .......................... Grantee ............................................ Estimated Total Annual Burden Hours: 983.44. Dated: December 22, 2016. Edwin L. Walker, Acting Administrator and Assistant Secretary for Aging. [FR Doc. 2016–31528 Filed 12–28–16; 8:45 am] BILLING CODE 4154–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2009–D–0524] Listing of Ingredients in Tobacco Products; Revised Guidance for Industry; Availability AGENCY: ACTION: Food and Drug Administration, Notice of availability. The Food and Drug Administration (FDA or we) is announcing the availability of a revised guidance for industry entitled ‘‘Listing of Ingredients in Tobacco Products.’’ The revised guidance document is intended to assist persons making tobacco product ingredient submissions to FDA as required by the Family Smoking Prevention and Tobacco Control Act (Tobacco Control Act). We received several comments to the draft guidance, and those comments were considered as the guidance was finalized. DATES: Submit either electronic or written comments on Agency guidances at any time. ADDRESSES: You may submit comments as follows: asabaliauskas on DSK3SPTVN1PROD with NOTICES SUMMARY: 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 VerDate Sep<11>2014 18:41 Dec 28, 2016 Jkt 241001 76 38 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 HHS. Submit written/paper submissions as follows: • Mail/Hand delivery/Courier (for written/paper submissions): Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Division of Dockets Management, 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– 2009–D–0524 for ‘‘Listing of Ingredients in Tobacco Products.’’ 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 Division of Dockets Management between 9 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 PO 00000 Frm 00048 Fmt 4703 Sfmt 4703 Responses per respondent Burden hours per response 2 2 4.67 3.6 Total burden hours (annual) 709.84 273.6. 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 Division of Dockets Management. 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: http://www.fda.gov/ regulatoryinformation/dockets/ default.htm. 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 Division of Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. Submit written requests for single copies of the revised draft guidance to the Center for Tobacco Products, Food and Drug Administration, Document Control Center, 10903 New Hampshire Ave., Bldg. 71, Rm. G335, Silver Spring, MD 20993–2000. Send one selfaddressed adhesive label to assist that office in processing your request or include a fax number to which the guidance document may be sent. See the SUPPLEMENTARY INFORMATION section for information on electronic access to the guidance document. FOR FURTHER INFORMATION CONTACT: Katherine Collins, Center for Tobacco Products, Food and Drug Administration, Document Control Center, 10903 New Hampshire Ave., Bldg. 71, Rm. G335, Silver Spring, MD 20993–2000, 1–877–287–1373, email: AskCTP@fda.hhs.gov. E:\FR\FM\29DEN1.SGM 29DEN1

Agencies

[Federal Register Volume 81, Number 250 (Thursday, December 29, 2016)]
[Notices]
[Pages 96002-96003]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-31528]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Community Living


Agency Information Collection Activities: Submission for OMB 
Review; Comment Request; Alzheimer's and Dementia Program Data 
Reporting Tool (ADP-DRT) (Previously Entitled: Alzheimer's Disease 
Supportive Services Program Data Reporting Tool (ADSSP-DRT) and 
Alzheimer's disease Initiative-- Specialized Supportive Services (ADI- 
SSS) project))

AGENCY: Administration for Community Living, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: In compliance with 44 U.S.C. 3507, the Administration on Aging 
(AoA), Administration for Community Living (ACL), is announcing that 
the proposed collection of information listed above has been submitted 
to the Office of Management and Budget (OMB) for review and clearance 
as required under the Paperwork Reduction Act of 1995. This notice 
collects comments on the information collection requirements relating 
to the continuation of an existing data collection for the Alzheimer's 
and Dementia Program Data Reporting Tool (ADP-PDR) and expansion of 
this collection to incorporate ACL grantees of the Alzheimer's Disease 
Initiative-- Specialized Supportive Services (ADI-SSS) project.

DATES: Submit written comments on the collection of information by 
January 30, 2017.

ADDRESSES: Submit written comments on the collection of information by 
fax to (202) 395-5806 or by email to OIRA_submission@omb.eop.gov, Attn: 
OMB Desk Officer for ACL.

FOR FURTHER INFORMATION CONTACT: Erin Long, (202) 795-7389; 
Erin.Long@acl.hhs.gov.

SUPPLEMENTARY INFORMATION: The Alzheimer's Disease Supportive Services 
Program (ADSSP) is authorized through Sections 398, 399 and 399A of the 
Public Health Service (PHS) Act, as amended by Public Law 101-557, the 
Home Health Care and Alzheimer's disease Amendments of 1990. The ADSSP 
helps state efforts to expand the availability of community-level 
supportive services for persons with Alzheimer's disease and their 
caregivers, including underserved populations. ADI-SSS projects are 
financed solely by Prevention and Public Health Funds. Similar in scope 
to ADSSP, ADI-SSS projects are designed to fill gaps in dementia-
capable home and community based services (HCBS) for persons living 
with or those at high risk of developing Alzheimer's disease and 
related dementias (ADRD) and their caregivers by providing quality, 
person-centered services that help them remain independent and safe in 
their communities. In compliance with the PHS Act, ACL revised the 
ADSSP Data Reporting Tool (ADSSP-DRT) in 2013 to add demographic data, 
information on the individuals trained, and service and expenditure 
data. The 2016 revised Alzheimer's and Dementia Program Data Reporting 
Tool (ADP-DRT) retains these changes and has been expanded to collect 
information about the delivery of direct services by both ADSSP and 
ADI-SSS grantees, as well as basic demographic information about 
service recipients.
    Comments in Response to the 60-Day Federal Register Notice:
    A 60-day Federal Register Notice was published in the Federal 
Register on August 23, 2016, Vol. 18, No. 136; pp. 57591. There was one 
public comment received pertaining to the categories for living 
arrangements. The comment suggested that the categories needed to have 
a clear definition. ACL accepted the comment, and the tool was revised 
by condensing the categories and providing an update to its definition 
of categories for living arrangements. The proposed ADP-DRT can be 
found on AoA's Web site at: https://nadrc.acl.gov/sites/default/files/uploads/docs/Proposed%20ADP-DRT%20Update%2011_30_2016.xlsx.
    Annual Burden Estimates: The estimated hourly burden for this 
revised ADP-DRT is based on the number of persons served in the most 
recent ADSSP and ADI grantee data

[[Page 96003]]

submission. In addition, the burden hours per response were determined 
based on reports from a sample of ADSSP and ADI grants.

----------------------------------------------------------------------------------------------------------------
                                     Type of         Number of     Responses per   Burden hours    Total burden
          Instrument               respondent       respondents     respondent     per response   hours (annual)
----------------------------------------------------------------------------------------------------------------
ADP-DRT.......................  Local Program                 76               2            4.67          709.84
                                 Site.
ADP-DRT.......................  Grantee.........              38               2             3.6          273.6.
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 983.44.

    Dated: December 22, 2016.
Edwin L. Walker,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2016-31528 Filed 12-28-16; 8:45 am]
 BILLING CODE 4154-01-P