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
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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:
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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]
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Fmt 4703
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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
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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]
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