Agency Information Collection Activities; Submission for OMB Review; Comment Request; Senior Medicare Patrol (SMP) Program Outcome Measurement, 35361-35362 [2016-12868]

Download as PDF 35361 Federal Register / Vol. 81, No. 106 / Thursday, June 2, 2016 / Notices Service, and the Public Health Agency of Canada. DATES: The webcast will be held over two days, August 3, 2016 from 12 p.m. to 4 p.m. EDT and August 4, 2016 from 12:00 p.m. to 4:00 p.m. Registration instructions are found on the HHS/CDC Import Permit Program Web site, https:// www.cdc.gov/od/eaipp/ importApplication/agents.htm. ADDRESSES: The webcast will be broadcast from the Centers for Disease Control and Prevention, 1600 Clifton Road NE., Atlanta, Georgia 30329. FOR FURTHER INFORMATION CONTACT: Von McClee, Division of Select Agents and Toxins, Office of Public Health Preparedness and Response, Centers for Disease Control and Prevention, 1600 Clifton Road, NE., MS A–46, Atlanta, GA 30333; phone: 404–718–2000; email: lrsat@cdc.gov. SUPPLEMENTARY INFORMATION: This webcast is an opportunity for all interested parties (e.g., academic institutions and biomedical centers, commercial manufacturing facilities, federal, state, and local laboratories, including clinical and diagnostic laboratories, research facilities, exhibition facilities, and educational facilities) to obtain specific guidance and information regarding import and export permit regulations. The webcast will also provide assistance to those interested in applying for an import or export permit (or license) from federal agencies within the United States. Instructions for registration are found on the HHS/CDC Import Permit Program Web site, https://www.cdc.gov/od/eaipp/ importApplication/agents.htm. Participants must register by July 15, 2016. This is a webcast only event and there will be no on-site participation at the HHS/CDC broadcast facility. Dated: May 27, 2016. Veronica Kennedy, Acting Executive Secretary, Centers for Disease Control and Prevention. [FR Doc. 2016–13053 Filed 6–1–16; 8:45 am] BILLING CODE 4163–18–P public comment in response to the notice. This notice collects comments on the information collection requirements relating to the continuation of an existing collection for University Centers for Excellence in Developmental Disabilities Education, Research, and Service. DATES: Submit written comments on the collection of information by August 1, 2016. Submit written comments on the collection of information by email to Valerie.Bond@acl.hhs.gov. FOR FURTHER INFORMATION CONTACT: Valerie Bond by email at Valerie.Bond@ acl.hhs.gov or 202.795–7311. SUPPLEMENTARY INFORMATION: Section 104 (42 U.S.C. 15004) of the Developmental Disabilities Assistance and Bill of Rights Act of 2000 (DD Act of 2000) directs the Secretary of Health and Human Services to develop and implement a system of program accountability to monitor the grantees funded under the DD Act of 2000. The program accountability system shall include the National Network of University Centers for Excellence in Developmental Disabilities Education, Research, and Service (UCEDDs) authorized under Part D of the DD Act of 2000. In addition to the accountability system, Section 154(e) (42 U.S.C. 15064) of the DD Act of 2000 includes requirements for a UCEDD Annual Report. ACL estimates the burden of this collection of information as follows: ADDRESSES: DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Community Living Agency Information Collection Activities: Submission for OMB Review; Comment Request; University Centers for Excellence in Developmental Disabilities Education, Research, and Service—Annual Report Administration for Community Living, HHS. ACTION: Notice. AGENCY: The Administration on Intellectual and Developmental Disabilities (AIDD), Administration for Community Living (ACL) is announcing an opportunity to comment on the proposed collection of 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 SUMMARY: Annual Burden Estimates ANNUAL BURDEN ESTIMATES Instrument Number of respondents Number of responses per respondent Average burden hours per response Total burden hours UCEDD Annual Report .................................................................................... 67 1 1,412 94,604 Estimated Total Annual Burden Hours: 94,604. Dated: May 25, 2016. Kathy Greenlee, Administrator & Assistant Secretary for Aging. asabaliauskas on DSK3SPTVN1PROD with NOTICES [FR Doc. 2016–13020 Filed 6–1–16; 8:45 am] BILLING CODE 4154–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Community Living Agency Information Collection Activities; Submission for OMB Review; Comment Request; Senior Medicare Patrol (SMP) Program Outcome Measurement Administration for Community Living, HHS. ACTION: Notice. AGENCY: The Administration for Community Living (ACL) is announcing that the proposed collection of SUMMARY: VerDate Sep<11>2014 18:30 Jun 01, 2016 Jkt 238001 PO 00000 Frm 00069 Fmt 4703 Sfmt 4703 information listed below has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. DATES: Submit written comments on the collection of information by July 5, 2016. Submit written comments on the collection of information by fax 202.395.5806 or by email to OIRA_ submission@omb.eop.gov. Attn: OMB Desk Officer for ACL. FOR FURTHER INFORMATION CONTACT: Phillip McKoy at 202.795.7397 or email: phillip.mckoy@acl.hhs.gov. ADDRESSES: E:\FR\FM\02JNN1.SGM 02JNN1 35362 Federal Register / Vol. 81, No. 106 / Thursday, June 2, 2016 / Notices In compliance with 44 U.S.C. 3507, ACL has submitted the following proposed collection of information to OMB for review and clearance. Grantees are required by Congress to provide information for use in program monitoring and for Government Performance and Results Act (GPRA) purposes. This information collection reports the number of active volunteers, issues and inquiries received, other SMP program outreach activities, and the number of Medicare dollars recovered, among other SMP performance outcomes. This information is used as the primary method for monitoring the SMP Projects. ACL estimates the burden of this collection of information as follows: Respondents: 54 SMP grantees at 23 hours per month (276 hours per year, per grantee). Total Estimated Burden Hours: 7,452 hours per year. SUPPLEMENTARY INFORMATION: Dated: May 25, 2016. Kathy Greenlee, Administrator and Assistant Secretary for Aging. [FR Doc. 2016–12868 Filed 6–1–16; 8:45 am] BILLING CODE 4154–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2016–N–0001] Collaborating To Strengthen Food, Drug, and Medical Device Safety Systems; Notice of Conference AGENCY: Food and Drug Administration, HHS. ACTION: Notice of conference. The Food and Drug Administration (FDA) Philadelphia District Office, in co-sponsorship with the Association of Food and Drug Officials (AFDO), and the North Central Association of Food and Drug Officials, is announcing a conference entitled ‘‘Collaborating to Strengthen Food, Drug, and Medical Device Safety Systems.’’ This conference is intended to provide information about FDA drug and device regulation to the regulated industry. asabaliauskas on DSK3SPTVN1PROD with NOTICES SUMMARY: The conference will be held on June 25 to June 29, 2016. See SUPPLEMENTARY INFORMATION for meeting times. ADDRESSES: The Omni William Penn Hotel, 530 William Penn Pl., Pittsburgh, PA 15219. Attendees are responsible for their own accommodations. DATES: VerDate Sep<11>2014 18:30 Jun 01, 2016 Jkt 238001 FOR FURTHER INFORMATION CONTACT: Randy Young, Association of Food and Drug Officials, 2550 Kingston Rd., Suite 311, York, PA 17402, 717–757–2888, FAX: 717–650–3650, ryoung@afdo.org. SUPPLEMENTARY INFORMATION: FDA has made education of the food, feed, drug, and device manufacturing community a high priority to help ensure the quality of FDA-regulated products. The conference helps to achieve objectives set forth in section 406 of the Food and Drug Administration Modernization Act of 1997 (21 U.S.C. 393), which includes working closely with stakeholders and maximizing the availability and clarity of information for stakeholders and the public. The conference also is consistent with the Small Business Regulatory Enforcement Fairness Act of 1996 (Pub. L. 104–121), as outreach activities by government Agencies to small businesses. The conference helps fulfill the U.S. Department of Health and Human Services’ and FDA’s important mission to protect the public health. The conference will provide FDA-regulated drug and device entities with information on a number of topics concerning FDA requirements related to the production and marketing of drugs and/or devices. Topics for discussion include, but are not limited to the following: • FDA Program Alignment • Recalls from the Perspective of the District • Inspection of Licensed Producers under the Marijuana for Medical Purposes Regulations (Health Canada) • Foreign inspections • Regulatory Intelligence • FDA Inspections: Challenges and Opportunities (Working Luncheon) • Drug Shortages • Drug Supply Chain Act: Wholesale Drug Distributor and 3rd Party Logistics Provider • Medical Device Single Audit Program • Compliance Questions Panel The Conference Web site is: https:// afdo.org/conference. The meeting times are as follows: Date June June June June June 25 26 27 28 29 Meeting time ....... ....... ....... ....... ....... 8 8 8 8 8 a.m. a.m. a.m. a.m. a.m. to to to to to 5 p.m. 6 p.m. 5:30 p.m. 5 p.m. 11:30 a.m. Registration: The AFDO registration fees cover the cost of facilities, materials, and breaks. Seats are limited and registration will close after the course is filled; therefore, please submit your registration as soon as possible. PO 00000 Frm 00070 Fmt 4703 Sfmt 4703 Conference space will be filled in order of receipt of registration; those accepted will receive confirmation. Registration at the site is not guaranteed but may be possible on a space available basis on the day of the conference, beginning at 7:30 a.m. The cost of registration follows: Category Cost of registration Member ................................... Non-Member ........................... Additional Fee for Registration Postmarked After June 1, 2016 .................................... $475 575 100 To register, please complete and submit an AFDO conference registration form, available at https://pitt.afdo.org/ registration.html, along with a check, money order payable to ‘‘AFDO’’; the registrar will also accept Visa and MasterCard credit cards. Please mail your completed registration form and payment to: AFDO, 2550 Kingston Rd., Suite 311, York, PA 17402. To register online, please visit https://pitt.afdo.org/ registration.html (FDA has verified the Web site address, but is not responsible for subsequent changes to the Web site after this document publishes in the Federal Register.) For more information on the conference, or for questions about registration, please contact Randy Young (see FOR FURTHER INFORMATION CONTACT), email inquiries will also be accepted at afdo@afdo.org, or visit https://www.afdo.org. If you need special accommodations due to a disability, please contact Randy Young (see FOR FURTHER INFORMATION CONTACT) at least 7 days in advance of the conference. Dated: May 26, 2016. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2016–12942 Filed 6–1–16; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2016–P–0378] Determination That TRIVARIS (Triamcinolone Acetonide) Injectable Suspension, 80 Milligrams/Milliliters, Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA or Agency) has SUMMARY: E:\FR\FM\02JNN1.SGM 02JNN1

Agencies

[Federal Register Volume 81, Number 106 (Thursday, June 2, 2016)]
[Notices]
[Pages 35361-35362]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-12868]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Community Living


Agency Information Collection Activities; Submission for OMB 
Review; Comment Request; Senior Medicare Patrol (SMP) Program Outcome 
Measurement

AGENCY: Administration for Community Living, HHS.

ACTION: Notice.

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

SUMMARY: The Administration for Community Living (ACL) is announcing 
that the proposed collection of information listed below has been 
submitted to the Office of Management and Budget (OMB) for review and 
clearance under the Paperwork Reduction Act of 1995.

DATES: Submit written comments on the collection of information by July 
5, 2016.

ADDRESSES: Submit written comments on the collection of information by 
fax 202.395.5806 or by email to OIRA_submission@omb.eop.gov. Attn: OMB 
Desk Officer for ACL.

FOR FURTHER INFORMATION CONTACT: Phillip McKoy at 202.795.7397 or 
email: phillip.mckoy@acl.hhs.gov.

[[Page 35362]]


SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, ACL has 
submitted the following proposed collection of information to OMB for 
review and clearance. Grantees are required by Congress to provide 
information for use in program monitoring and for Government 
Performance and Results Act (GPRA) purposes. This information 
collection reports the number of active volunteers, issues and 
inquiries received, other SMP program outreach activities, and the 
number of Medicare dollars recovered, among other SMP performance 
outcomes. This information is used as the primary method for monitoring 
the SMP Projects. ACL estimates the burden of this collection of 
information as follows: Respondents: 54 SMP grantees at 23 hours per 
month (276 hours per year, per grantee). Total Estimated Burden Hours: 
7,452 hours per year.

    Dated: May 25, 2016.
Kathy Greenlee,
Administrator and Assistant Secretary for Aging.
[FR Doc. 2016-12868 Filed 6-1-16; 8:45 am]
 BILLING CODE 4154-01-P
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