Proposed Information Collection Activity; Comment Request, 78363-78364 [2013-30809]
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Federal Register / Vol. 78, No. 248 / Thursday, December 26, 2013 / Notices
Dated: December 19, 2013.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2013–30905 Filed 12–24–13; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[CDC–2013–0021; NIOSH 245–A]
Notice of Request for Comments on
Chapters 6 and 8 of the NIOSH
document titled: ‘‘Criteria for a
Recommended Standard:
Occupational Exposure to Diacetyl and
2,3-pentanedione’’
National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Request for Comments.
AGENCY:
The National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC) is inviting
comments on Chapter 6 and a new
section of Chapter 8 of the draft
document, ‘‘Criteria for a
Recommended Standard: Occupational
Exposure to Diacetyl and 2,3pentanedione.’’ To view the notice and
related materials, visit https://
www.regulations.gov and enter CDC–
2013–0021 in the search field and click
‘‘Search.’’ Public Comment Period:
Comments must be received by February
10, 2014.
Status: Comments are being sought
from individuals including scientists
and representatives from various
government agencies, industry, labor,
and other stakeholders, and also the
public.
SUMMARY:
You may submit comments,
identified by CDC–2013–0021 and
Docket Number NIOSH 245–A by either
of the following two methods:
Federal rulemaking portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Mail: NIOSH Docket Office, Robert A.
Taft Laboratories, 4676 Columbia
Parkway, MS–C34, Cincinnati, Ohio
45226.
Instructions: All information received
in response to this notice must include
the agency name and docket number
[CDC–2013–0021; NIOSH 245–A]. All
relevant comments received, including
any personal information provided, will
be posted without change to https://
www.regulations.gov. All electronic
comments should be formatted as
Microsoft Word. Please make reference
to CDC–2013–0021 and Docket Number
NIOSH 245–A. To access the docket,
read background documents or read
comments, go to https://
www.regulations.gov. To access any
prior background documents or
previous comments received please go
to NIOSH Docket 245 (https://
www.cdc.gov/niosh/docket/archive/
docket245.html). All information
received in response to this notice will
be available for public examination and
copying at the NIOSH Docket Office,
4676 Columbia Parkway, Cincinnati,
Ohio 45226.
ADDRESSES:
FOR MORE INFORMATION CONTACT:
Lauralynn Taylor McKernan, ScD CIH
NIOSH, 4676 Columbia Parkway C–14,
Cincinnati, OH 45226, telephone (513)
533–8542, Fax (513) 533–8588, email
LMcKernan@cdc.gov.
Dated: December 19, 2013.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects: To establish a
systematic method of reporting suicides
and suicide attempts by refugees.
Title: Refugee Suicide Report Form
(RSR).
OMB No.: 0970–NEW.
Description
Pursuant to section 412(b)(4) of the
Immigration and Nationality Act, the
Administration for Children and
Families’ Office of Refugee Resettlement
(ORR), as the designee for the Secretary
of Health and Human Services, is
authorized to identify and monitor
refugees with certain medical
conditions that affect the public health
and require treatment.
The intent of this collection activity is
to allow ORR to systematically gather
information on suicides and suicide
attempts among refugee populations
resettled in the U.S. Data will be
collected on individuals who have made
suicide attempts or completed a suicide.
The data will be analyzed to identify
trends and factors related to suicidal
behavior. In addition, the data will be
used to plan, implement, and evaluate
suicide prevention and intervention
activities, in collaboration with local,
state, and national government agencies
and organizations serving the refugee
population.
Respondents: State Governments.
[FR Doc. 2013–30900 Filed 12–24–13; 8:45 am]
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ANNUAL BURDEN ESTIMATES
Instrument
emcdonald on DSK67QTVN1PROD with NOTICES
Refugee Suicide Report Form (RSR) .............
Estimated Total Annual Burden
Hours:
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
VerDate Mar<15>2010
18:06 Dec 24, 2013
Number of
responses per
respondent
Jkt 232001
100 or more
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
Average
burden hours
per response
Total burden
hours
1
Number of respondents
0.5
50
Attn: ACF Reports Clearance Officer.
Email address: infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
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Federal Register / Vol. 78, No. 248 / Thursday, December 26, 2013 / Notices
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013–30809 Filed 12–24–13; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–1620]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Information From
United States Firms and Processors
That Export to the European
Community
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or we) is
announcing an opportunity for public
comment on the proposed collection of
certain 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 public comment in
response to the notice. This notice
solicits comments on reporting
requirements in implementing the lists
of United States (U.S.) firms/processors
exporting shell eggs, dairy products,
game meat, game meat products, animal
casings, gelatin, and collagen to the
European Community (the EC).
DATES: Submit either electronic or
written comments on the collection of
information by February 24, 2014.
ADDRESSES: Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
emcdonald on DSK67QTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
18:06 Dec 24, 2013
Jkt 232001
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 1350 Piccard
Dr., PI50–400B, Rockville, MD 20850,
PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
Agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
Agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
Information From United States Firms
and Processors That Export to the
European Community (OMB Control
Number 0910–0320)—Extension
The EC is a group of 27 European
countries that have agreed to harmonize
their commodity requirements to
facilitate commerce among member
States. EC legislation for intra-EC trade
has been extended to trade with non-EC
countries, including the United States.
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
For certain food products, including
those listed in this document, EC
legislation requires assurances from the
responsible authority of the country of
origin that the processor of the food is
in compliance with applicable
regulatory requirements. The European
Commission, the executive branch of
the EC, requires countries trading with
any of the EC member countries to
provide lists of firms and processors
approved to export certain animalderived commodities to the EC. As
stated in the notice published in the
Federal Register of April 4, 1996 (61 FR
15077), we established a list of U.S.
firms and processors that intended to
export shell eggs, dairy products, and
game meat and game meat products to
the EC.
Although our 1996 Federal Register
notice did not include on the list firms
and processors exporting gelatin and
raw, bulk collagen intended for human
consumption, EC directives require that
shipments of gelatin and raw, bulk
collagen products be accompanied by
certification stating that the product,
derived from ruminant bones, bovine
hides, and pigskins, has been produced
in compliance with EC Council
Directive 2003/863/EC. The directive
contains the requirements for sourcing,
manufacture, transport, and storage of
raw materials and manufacture of
finished products and requires lists
identifying non-EC firms and processors
that meet EC requirements and have the
appropriate animal and public health
certificates. Therefore, we revised this
information collection in order to
facilitate exports of gelatin and raw,
bulk collagen originating from the
United States into the EC. We
announced OMB approval of the revised
information collection in the Federal
Register of May 10, 2011 (76 FR 27061).
We request the following information
from each firm or processor seeking to
be included on the lists for shell eggs,
dairy products, game meat, game meat
products, and animal casings:
• Business name and address;
• Name and telephone number of
person designated as business contact;
• Lists of products presently being
shipped to the EC and those intended to
be shipped in the next 6 months;
• Name and address of manufacturing
plants for each product; and
• Names and affiliations of any
Federal, State, or local governmental
Agencies that inspect the plant,
government-assigned plant identifier
such as plant number, and last date of
inspection.
We use the information to maintain
lists of firms and processors that have
demonstrated current compliance with
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]]>Agencies
[Federal Register Volume 78, Number 248 (Thursday, December 26, 2013)]
[Notices]
[Pages 78363-78364]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-30809]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects: To establish a systematic method of reporting
suicides and suicide attempts by refugees.
Title: Refugee Suicide Report Form (RSR).
OMB No.: 0970-NEW.
Description
Pursuant to section 412(b)(4) of the Immigration and Nationality
Act, the Administration for Children and Families' Office of Refugee
Resettlement (ORR), as the designee for the Secretary of Health and
Human Services, is authorized to identify and monitor refugees with
certain medical conditions that affect the public health and require
treatment.
The intent of this collection activity is to allow ORR to
systematically gather information on suicides and suicide attempts
among refugee populations resettled in the U.S. Data will be collected
on individuals who have made suicide attempts or completed a suicide.
The data will be analyzed to identify trends and factors related to
suicidal behavior. In addition, the data will be used to plan,
implement, and evaluate suicide prevention and intervention activities,
in collaboration with local, state, and national government agencies
and organizations serving the refugee population.
Respondents: State Governments.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of respondents responses per hours per Total burden
respondent response hours
----------------------------------------------------------------------------------------------------------------
Refugee Suicide Report Form (RSR)... 100 or more 1 0.5 50
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours:
In compliance with the requirements of Section 506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Planning, Research and Evaluation, 370 L'Enfant Promenade SW.,
Washington, DC 20447, Attn: ACF Reports Clearance Officer. Email
address: infocollection@acf.hhs.gov. All requests should be identified
by the title of the information collection.
The Department specifically requests comments on: (a) Whether the
proposed collection of information is necessary
[[Page 78364]]
for the proper performance of the functions of the agency, including
whether the information shall have practical utility; (b) the accuracy
of the agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013-30809 Filed 12-24-13; 8:45 am]
BILLING CODE 4184-01-P
