Agency Information Collection Activities; Submission to OMB for Review and Approval; Public Comment Request, 77355-77356 [2015-31355]

Download as PDF Federal Register / Vol. 80, No. 239 / Monday, December 14, 2015 / Notices if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Email: OIRA_ SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration for Children and Families. Robert Sargis, Reports Clearance Officer. [FR Doc. 2015–31314 Filed 12–11–15; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2015–N–0001] Circulatory System Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting AGENCY: Food and Drug Administration, HHS. mstockstill on DSK4VPTVN1PROD with NOTICES ACTION: Notice. This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). The meeting will be open to the public. Name of Committee: Circulatory System Devices Panel of the Medical Devices Advisory Committee. General Function of the Committee: To provide advice and recommendations to the Agency on FDA’s regulatory issues. Date and Time: The meeting will be held on Thursday, February 18, 2016, from 8 a.m. to 6 p.m. Location: Hilton Washington DC North/Gaithersburg, Salons A, B, C, and D, 620 Perry Pkwy., Gaithersburg, MD 20877. The hotel telephone number is 301–977–8900. Contact Person: Dimitrus Culbreath, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 1535, Silver Spring, MD, 20993, Dimitrus.Culbreath@fda.hhs.gov, 301– 796–6872, or FDA Advisory Committee Information Line, 1–800–741–8138 (301–443–0572 in the Washington, DC area). A notice in the Federal Register about last minute modifications that impact a previously announced advisory committee meeting cannot always be published quickly enough to provide timely notice. Therefore, you should always check the Agency’s Web site at https://www.fda.gov/Advisory Committees/default.htm and scroll VerDate Sep<11>2014 17:36 Dec 11, 2015 Jkt 238001 down to the appropriate advisory committee meeting link, or call the advisory committee information line to learn about possible modifications before coming to the meeting. Agenda: The Committee will discuss and make recommendations on clinical trial, postapproval study design, and physician training requirements for leadless cardiac pacemaker device technology. Specifically, the Committee will be asked to make recommendations on the acceptability of adverse event rates in acute and chronic timeframes as well as indications for use for this device type, given availability of other technologies with different adverse event profiles; required training and acceptability of observed learning curves for the new device type and necessary elements for postapproval study collection. FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its Web site prior to the meeting, the background material will be made publicly available at the location of the advisory committee meeting, and the background material will be posted on FDA’s Web site after the meeting. Background material is available at https://www.fda.gov/ AdvisoryCommittees/Calendar/ default.htm. Scroll down to the appropriate advisory committee meeting link. Procedure: Interested persons may present data, information, or views, orally or in writing, on issues pending before the committee. Written submissions may be made to the contact person on or before February 11, 2016. Oral presentations from the public will be scheduled between approximately 1 p.m. and 2 p.m. Those individuals interested in making formal oral presentations should notify the contact person and submit a brief statement of the general nature of the evidence or arguments they wish to present, the names and addresses of proposed participants, and an indication of the approximate time requested to make their presentation on or before February 3, 2016. Time allotted for each presentation may be limited. If the number of registrants requesting to speak is greater than can be reasonably accommodated during the scheduled open public hearing session, FDA may conduct a lottery to determine the speakers for the scheduled open public hearing session. The contact person will notify interested persons regarding their request to speak by February 4, 2016. Persons attending FDA’s advisory committee meetings are advised that the PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 77355 Agency is not responsible for providing access to electrical outlets. FDA welcomes the attendance of the public at its advisory committee meetings and will make every effort to accommodate persons with disabilities. If you require accommodations due to a disability, please contact Artair Mallett at 301–796–9638, at least 7 days in advance of the meeting. FDA is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at https://www.fda.gov/Advisory Committees/AboutAdvisoryCommittees/ ucm111462.htm for procedures on public conduct during advisory committee meetings. Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app. 2). Dated: December 8, 2015. Jill Hartzler Warner, Associate Commissioner for Special Medical Programs. [FR Doc. 2015–31372 Filed 12–11–15; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the Secretary [Document Identifier: HHS–OS–0990–New– 30D] Agency Information Collection Activities; Submission to OMB for Review and Approval; Public Comment Request Office of the Secretary, HHS. Notice. AGENCY: ACTION: In compliance with section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the Office of the Secretary (OS), Department of Health and Human Services, has submitted an Information Collection Request (ICR), described below, to the Office of Management and Budget (OMB) for review and approval. The ICR is for a new collection. Comments submitted during the first public review of this ICR will be provided to OMB. OMB will accept further comments from the public on this ICR during the review and approval period. DATES: Comments on the ICR must be received on or before January 13, 2016. ADDRESSES: Submit your comments to OIRA_submission@omb.eop.gov or via facsimile to (202) 395–5806. FOR FURTHER INFORMATION CONTACT: Information Collection Clearance staff, Information.CollectionClearance@ hhs.gov or (202) 690–6162. SUMMARY: E:\FR\FM\14DEN1.SGM 14DEN1 77356 Federal Register / Vol. 80, No. 239 / Monday, December 14, 2015 / Notices When submitting comments or requesting information, please include the Information Collection Request Title and document identifier HHS–OS– 0990–New–30D for reference. SUPPLEMENTARY INFORMATION: Information Collection Request Title: Privacy and Security Capacity Assessment of the Title X Network Abstract: The Office of the Assistant Secretary for Health Office of Population Affairs, (OPA) is requesting an approval by Office of Management and Budget (OMB) for a new information collection (Privacy and Security Capacity Assessment) which seeks to collect feedback from the Title X network regarding Title X grantees’ and service sites’ current privacy and security capabilities for health information exchange. This voluntary form will be administered at most annually and enable the Title X network to share important information to critically inform OPA’s development of Family Planning Annual Report (FPAR 2.0), as well as identify any training assistance and inform guidance that OPA may offer in the future. OPA will solicit feedback from Title X agencies to advise our work on privacy and security, and proposes to make this data collection form available for up to 3 years so that OPA can accept feedback from the network regarding any changes or trends that might alter our approach to privacy and security as we proceed through the design and build process for the planned FPAR 2.0 data repository. Likely Respondents: Title X Grantees, Subrecipients, and Service Sites. TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS Type of respondent Grantees ...................................... Service Sites ................................ Totals .................................... Sustainability Grantees. Sustainability Sites. 92 Grantees ..... 1 Assessment— 4,168 ................ 1 ..................................................... 4,260 ................ BILLING CODE 4150–28–P DEPARTMENT OF HOMELAND SECURITY U.S. Customs and Border Protection Customs Brokers User Fee Payment for 2016 U.S. Customs and Border Protection, Department of Homeland Security. ACTION: General notice. AGENCY: This document provides notice to customs brokers that the annual user fee of $138 that is assessed for each permit held by a broker, whether it may be an individual, partnership, association, or corporation, is due by February 26, 2016. DATES: Payment of the 2016 Customs Broker User Fee is due by February 26, 2016. FOR FURTHER INFORMATION CONTACT: Julia Peterson, Broker Management Branch, Office of International Trade, (202) 863– 6601. SUPPLEMENTARY INFORMATION: Pursuant to section 111.96 of title 19 of the Code of Federal Regulations (19 CFR 111.96(c)), U.S. Customs and Border Protection (CBP) assesses an annual user fee of $138 for each customs broker SUMMARY: mstockstill on DSK4VPTVN1PROD with NOTICES Average annualized burden per response (hours) ........................ [FR Doc. 2015–31355 Filed 12–11–15; 8:45 am] 17:36 Dec 11, 2015 Number of responses per respondent Assessment— Terry S. Clark, Asst. Information Collection Clearance Officer. VerDate Sep<11>2014 Number of respondents Form name Jkt 238001 district and national permit held by an individual, partnership, association, or corporation. CBP regulations provide that this fee is payable for each calendar year in each broker district where the broker was issued a permit to do business by the due date. See 19 CFR 24.22(h) and (i)(9). Broker districts are defined in the General Notice entitled, ‘‘Geographic Boundaries of Customs Brokerage, Cartage and Lighterage Districts,’’ published in the Federal Register on March 15, 2000 (65 FR 14011), and corrected, with minor changes, on March 23, 2000 (65 FR 15686) and on April 6, 2000 (65 FR 18151). As required by 19 CFR 111.96, CBP must provide notice in the Federal Register no later than 60 days before the date that the payment is due for each broker permit. This document notifies customs brokers that for calendar year 2016, the due date for payment of the user fee is February 26, 2016. It is anticipated that for subsequent years, the annual user fee for customs brokers will be due on the last business day of February of each year. Dated: December 9, 2015. Brenda B. Smith, Assistant Commissioner, Office of International Trade. [FR Doc. 2015–31370 Filed 12–11–15; 8:45 am] BILLING CODE 9111–14–P PO 00000 Frm 00043 Fmt 4703 Sfmt 4703 Annualized total burden (hours) 40 minutes (0.66 hours). 40 minutes (0.66 hours). 60.72 2,750.88 ................................ 2811.60 DEPARTMENT OF HOMELAND SECURITY Federal Emergency Management Agency [Docket ID FEMA–2015–0001] Final Flood Hazard Determinations Federal Emergency Management Agency, DHS. ACTION: Final notice. AGENCY: Flood hazard determinations, which may include additions or modifications of Base Flood Elevations (BFEs), base flood depths, Special Flood Hazard Area (SFHA) boundaries or zone designations, or regulatory floodways on the Flood Insurance Rate Maps (FIRMs) and where applicable, in the supporting Flood Insurance Study (FIS) reports have been made final for the communities listed in the table below. The FIRM and FIS report are the basis of the floodplain management measures that a community is required either to adopt or to show evidence of having in effect in order to qualify or remain qualified for participation in the Federal Emergency Management Agency’s (FEMA’s) National Flood Insurance Program (NFIP). In addition, the FIRM and FIS report are used by insurance agents and others to calculate appropriate flood insurance premium rates for buildings and the contents of those buildings. DATES: The effective date of April 5, 2016 which has been established for the SUMMARY: E:\FR\FM\14DEN1.SGM 14DEN1

Agencies

[Federal Register Volume 80, Number 239 (Monday, December 14, 2015)]
[Notices]
[Pages 77355-77356]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-31355]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Office of the Secretary

[Document Identifier: HHS-OS-0990-New-30D]


Agency Information Collection Activities; Submission to OMB for 
Review and Approval; Public Comment Request

AGENCY: Office of the Secretary, HHS.

ACTION: Notice.

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

SUMMARY: In compliance with section 3507(a)(1)(D) of the Paperwork 
Reduction Act of 1995, the Office of the Secretary (OS), Department of 
Health and Human Services, has submitted an Information Collection 
Request (ICR), described below, to the Office of Management and Budget 
(OMB) for review and approval. The ICR is for a new collection. 
Comments submitted during the first public review of this ICR will be 
provided to OMB. OMB will accept further comments from the public on 
this ICR during the review and approval period.

DATES: Comments on the ICR must be received on or before January 13, 
2016.

ADDRESSES: Submit your comments to OIRA_submission@omb.eop.gov or via 
facsimile to (202) 395-5806.

FOR FURTHER INFORMATION CONTACT: Information Collection Clearance 
staff, Information.CollectionClearance@hhs.gov or (202) 690-6162.

[[Page 77356]]


SUPPLEMENTARY INFORMATION: When submitting comments or requesting 
information, please include the Information Collection Request Title 
and document identifier HHS-OS-0990-New-30D for reference.

Information Collection Request Title: Privacy and Security Capacity 
Assessment of the Title X Network

    Abstract: The Office of the Assistant Secretary for Health Office 
of Population Affairs, (OPA) is requesting an approval by Office of 
Management and Budget (OMB) for a new information collection (Privacy 
and Security Capacity Assessment) which seeks to collect feedback from 
the Title X network regarding Title X grantees' and service sites' 
current privacy and security capabilities for health information 
exchange. This voluntary form will be administered at most annually and 
enable the Title X network to share important information to critically 
inform OPA's development of Family Planning Annual Report (FPAR 2.0), 
as well as identify any training assistance and inform guidance that 
OPA may offer in the future. OPA will solicit feedback from Title X 
agencies to advise our work on privacy and security, and proposes to 
make this data collection form available for up to 3 years so that OPA 
can accept feedback from the network regarding any changes or trends 
that might alter our approach to privacy and security as we proceed 
through the design and build process for the planned FPAR 2.0 data 
repository.
    Likely Respondents: Title X Grantees, Subrecipients, and Service 
Sites.

                                    Total Estimated Annualized Burden--Hours
----------------------------------------------------------------------------------------------------------------
                                                                                     Average
                                                                    Number of       annualized      Annualized
      Type of respondent          Form name        Number of      responses per     burden per     total burden
                                                  respondents      respondent        response         (hours)
                                                                                     (hours)
----------------------------------------------------------------------------------------------------------------
Grantees.....................  Sustainability   92 Grantees....               1  40 minutes                60.72
                                Assessment--Gr                                    (0.66 hours).
                                antees.
Service Sites................  Sustainability   4,168..........               1  40 minutes             2,750.88
                                Assessment--Si                                    (0.66 hours).
                                tes.
                                               -----------------------------------------------------------------
    Totals...................  ...............  4,260..........  ..............  ...............         2811.60
----------------------------------------------------------------------------------------------------------------


Terry S. Clark,
Asst. Information Collection Clearance Officer.
[FR Doc. 2015-31355 Filed 12-11-15; 8:45 am]
 BILLING CODE 4150-28-P
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