Agency Information Collection Activities; Submission to OMB for Review and Approval; Public Comment Request, 48437-48438 [2013-19137]
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48437
Federal Register / Vol. 78, No. 153 / Thursday, August 8, 2013 / Notices
information, processing and
maintaining information, and disclosing
and providing information, to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information, and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
responses per
respondent
Number of
respondents
Form name
Average
burden per
response
(in hours)
Total burden
hours
Applications for surplus Federal real property .................................................
12
1
200
2,400
Total ..........................................................................................................
12
1
200
2,400
OS specifically requests comments on
(1) The necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Darius Taylor,
Deputy, Information Collection Clearance
Officer.
BILLING CODE 4151–17–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS–OS–19201–30D]
Agency Information Collection
Activities; Submission to OMB for
Review and Approval; Public Comment
Request
Office of the Secretary, HHS.
Notice.
AGENCY:
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),
SUMMARY:
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.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the OMB
control number 0990–0001 and
document identifier HHS–OS–19201–
30D for reference.
Information Collection Request Title:
Application for waiver of the two year
foreign residence requirement of the
Exchange Visitor Program.
OMB No.: 0990–0001
Abstract: The HHS program deals
with both research and clinical care
waivers. Applicant institutions apply to
this Department to request a waiver on
behalf of research scientists or foreign
ADDRESSES:
[FR Doc. 2013–19135 Filed 8–7–13; 8:45 am]
ACTION:
medical graduates to work as clinicians
in HHS designated health shortage areas
doing primary care in medical facilities.
The instructions request a copy of Form
G–28 from applicant institutions
represented by legal counsel outside of
the applying institution. United States
Department of Justice Form G–28
ascertains that legal counsel represents
both the applicant organization and the
exchange visitor.
Need and Proposed Use of the
Information: Required as part of the
application process to collect basic
information such as name, address,
family status, sponsor and current visa
information.
Likely Respondents: Research
scientists and research facilities.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes the time
needed to review instructions, to
develop, acquire, install and utilize
technology and systems for the purpose
of collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information, to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information, and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
described below, to the Office of
Management and Budget (OMB) for
review and approval. The ICR is for
renewal of the approved information
collection assigned OMB control
number 0990–0001, scheduled to expire
on September 30, 2013. 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 September 9,
2013.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
tkelley on DSK3SPTVN1PROD with NOTICES
Type of respondent
Form name
Application Waiver/Supplemental A Research ......................
Application Waiver/Supplemental B Clinical Care .................
HHS 426 .....
HHS 426 .....
45
35
1
1
10
10
450
350
Total ................................................................................
.....................
........................
........................
........................
800
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48438
Federal Register / Vol. 78, No. 153 / Thursday, August 8, 2013 / Notices
Darius Taylor,
Deputy, Information Collection Clearance
Officer.
[FR Doc. 2013–19137 Filed 8–7–13; 8:45 am]
BILLING CODE 4150–38–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
tkelley on DSK3SPTVN1PROD with NOTICES
Board of Scientific Counselors,
National Center for Health Statistics
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC), National
Center for Health Statistics (NCHS)
announces the following meeting of the
aforementioned committee:
Times and Dates:
11:00 a.m.–5:30 p.m., September 19,
2013
8:30 a.m.–1:00 p.m., September 20, 2013
Place: NCHS Headquarters, 3311
Toledo Road, Hyattsville, Maryland
20782.
Status: This meeting is open to the
public; however, visitors must be
processed in accordance with
established federal policies and
procedures. For foreign nationals or
non-US citizens, pre-approval is
required (please contact Gwen Mustaf,
301–458–4500, glm4@cdc.gov or
Virginia Cain, vcain@cdc.gov at least 10
days in advance for requirements). All
visitors are required to present a valid
form of picture identification issued by
a state, federal or international
government. As required by the Federal
Property Management Regulations, Title
41, Code of Federal Regulation, Subpart
101–20.301, all persons entering in or
on Federal controlled property and their
packages, briefcases, and other
containers in their immediate
possession are subject to being x-rayed
and inspected. Federal law prohibits the
knowing possession or the causing to be
present of firearms, explosives and other
dangerous weapons and illegal
substances. The meeting room
accommodates approximately 100
people.
Purpose: This committee is charged
with providing advice and making
recommendations to the Secretary,
Department of Health and Human
Services; the Director, CDC; and the
Director, NCHS, regarding the scientific
and technical program goals and
objectives, strategies, and priorities of
NCHS.
Matters to be Discussed: The agenda
will include welcome remarks by the
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Acting Director, NCHS; Demo of the
NHIS Online Analytic Real-time System
(OARS); initiation of Office of Analysis
and Epidemiology review.
Requests to make oral presentations
should be submitted in writing to the
contact person listed below. All requests
must contain the name, address,
telephone number, and organizational
affiliation of the presenter.
Written comments should not exceed
five single-spaced typed pages in length
and must be received by September 4,
2013.
The agenda items are subject to
change as priorities dictate.
Contact Person for more Information:
Virginia S. Cain, Ph.D., Director of
Extramural Research, NCHS/CDC, 3311
Toledo Road, Room 7208, Hyattsville,
Maryland 20782, telephone (301) 458–
4500, fax (301) 458–4020.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities for both Centers
for Disease Control and Prevention and
the Agency for Toxic Substances and
Disease Registry.
Elaine L. Baker,
Management Analysis and Services Office,
Centers for Disease Control and Prevention.
[FR Doc. 2013–19156 Filed 8–7–13; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0001]
Pediatric Ethics Subcommittee of the
Pediatric Advisory Committee; Notice
of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a subcommittee of a public
advisory committee of the Food and
Drug Administration (FDA). The
meeting will be open to the public.
Name of Subcommittee: Pediatric
Ethics Subcommittee of the Pediatric
Advisory Committee.
General Function of the
Subcommittee: To advise and make
recommendations to the Pediatric
Advisory Committee on pediatric
ethical issues.
Date and Time: The meeting will be
held on September 9, 2013, from 8 a.m.
to 5:30 p.m. and September 10, 2013,
from 8 a.m. to 3 p.m.
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Location: Doubletree Hilton Hotel,
8727 Colesville Rd., Silver Spring, MD
20910, 301–589–5200 or visit the hotel’s
Web site at https://
doubletree3.hilton.com/en/hotels/
maryland/doubletree-by-hilton-hotelwashington-dc-silver-spring-DCASSDT/
index.html.
Contact Person: Walter Ellenberg,
Office of the Commissioner, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 32, rm. 5154,
Silver Spring, MD 20993, 301–796–
0885, email
walter.ellenberg@fda.hhs.gov 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 subcommittee 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/AdvisoryCommittees/
default.htm and scroll 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: On September 9 and 10,
2013, the Pediatric Ethics Subcommittee
of the Pediatric Advisory Committee
will meet to discuss ethical issues in
pediatric product development,
including medical counter measures,
focusing on the concepts of minimal
risk, disorder or condition, and
exposure of pediatric subjects to risks
under 21 CFR 50.54.
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 subcommittee 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 September 9, 2013.
Oral presentations from the public will
be scheduled between approximately 2
p.m. and 3 p.m. Those individuals
interested in making formal oral
presentations should notify the contact
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]]>Agencies
[Federal Register Volume 78, Number 153 (Thursday, August 8, 2013)]
[Notices]
[Pages 48437-48438]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-19137]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS-OS-19201-30D]
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 renewal of the approved
information collection assigned OMB control number 0990-0001, scheduled
to expire on September 30, 2013. 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 September 9,
2013.
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.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the OMB control number 0990-0001 and
document identifier HHS-OS-19201-30D for reference.
Information Collection Request Title: Application for waiver of the
two year foreign residence requirement of the Exchange Visitor Program.
OMB No.: 0990-0001
Abstract: The HHS program deals with both research and clinical
care waivers. Applicant institutions apply to this Department to
request a waiver on behalf of research scientists or foreign medical
graduates to work as clinicians in HHS designated health shortage areas
doing primary care in medical facilities. The instructions request a
copy of Form G-28 from applicant institutions represented by legal
counsel outside of the applying institution. United States Department
of Justice Form G-28 ascertains that legal counsel represents both the
applicant organization and the exchange visitor.
Need and Proposed Use of the Information: Required as part of the
application process to collect basic information such as name, address,
family status, sponsor and current visa information.
Likely Respondents: Research scientists and research facilities.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose or provide the
information requested. This includes the time needed to review
instructions, to develop, acquire, install and utilize technology and
systems for the purpose of collecting, validating and verifying
information, processing and maintaining information, and disclosing and
providing information, to train personnel and to be able to respond to
a collection of information, to search data sources, to complete and
review the collection of information, and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this ICR are summarized in the table below.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
Application Waiver/ HHS 426.......... 45 1 10 450
Supplemental A Research.
Application Waiver/ HHS 426.......... 35 1 10 350
Supplemental B Clinical Care.
----------------------------------------------------------------------------------
Total.................... ................. .............. .............. .............. 800
----------------------------------------------------------------------------------------------------------------
[[Page 48438]]
Darius Taylor,
Deputy, Information Collection Clearance Officer.
[FR Doc. 2013-19137 Filed 8-7-13; 8:45 am]
BILLING CODE 4150-38-P
