Submission for OMB Review; Comment Request, 12497-12498 [2016-05240]
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Federal Register / Vol. 81, No. 46 / Wednesday, March 9, 2016 / Notices
Prevention and the Agency for Toxic
Substances and Disease Registry.
Catherine Ramadei,
Acting Director, Management Analysis and
Services Office Centers for Disease Control
and Prevention.
[FR Doc. 2016–05265 Filed 3–8–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Advisory Committee to the Director
(ACD), Centers for Disease Control and
Prevention—State, Tribal, Local and
Territorial (STLT) Subcommittee
Meeting
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)
announces the following meeting of the
aforementioned subcommittee:
Time and Date: 11:30 a.m.–1:00 p.m.
EDT, April 08, 2016.
Place: This meeting will be held by
teleconference.
Status: This meeting is open to the
public, limited only by the availability
of telephone ports. The public is
welcome to participate during the
public comment, which is tentatively
scheduled from 12:40 p.m. to 12:45 p.m.
To participate on the teleconference,
please dial (888) 233–0592 and enter
code 33288611.
Purpose: The Subcommittee will
provide advice to the CDC Director
through the ACD on strategies and
future needs and challenges faced by
State, Tribal, Local and Territorial
health agencies, and will provide
guidance on opportunities for CDC.
Matters for Discussion: The STLT
Subcommittee members will discuss
progress on implementation of ACDadopted recommendations related to the
health departments of the future,
additional developments that may
expand these recommendations, and
how CDC can best support STLT health
departments.
The agenda is subject to change as
priorities dictate.
Contact Person for More Information:
John Auerbach, MBA, Designated
Federal Officer, STLT Subcommittee,
ACD, CDC, 4770 Buford Highway, MS
E70, Atlanta, Georgia 30341, Telephone
(404) 498–0300, Email:
OSTLTSDirector@cdc.gov. Please
submit comments to OSTLTSDirector@
cdc.gov by April 1, 2016.
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 the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Claudette Grant,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention.
[FR Doc. 2016–05264 Filed 3–8–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Evaluation of Domestic Human
Trafficking Demonstration Projects.
OMB No.: New Collection.
Description: The Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services (HHS) is proposing a 2-year
data collection as part of the
‘‘Evaluation of Domestic Human
Trafficking Demonstration Projects’’
study. This notice addresses the crosssite process evaluation to be conducted
with the FY 2015 domestic human
trafficking demonstration sites funded
by the Family and Youth Services
Bureau (FYSB).
The objective of the process
evaluation is to describe program
operations and implementation
experience, such as start-up efforts,
service provision to a wide array of
trafficking victims, collaboration
development, training, and
sustainability actions. Information from
the evaluation will assist federal, state,
and community policymakers and
funders in laying the groundwork for
the refinement of program models to
serve domestic victims of human
trafficking, as well as evaluation
strategies for future programs targeting
trafficking victims.
The evaluation of domestic human
trafficking demonstration projects will
document and describe each site’s
community and organizational capacity;
partnership composition and
functioning; comprehensive, victimcentered services; and survivor
characteristics, experiences, and
outcomes. Primary data for the
evaluation will be collected via
qualitative interviews, including key
informant interviews, case narrative
interviews, client interviews, bimonthly
telephone interviews, and cost modules
(i.e., structured interviews with project
directors to collect information on
costs). Data will be collected via two site
visits per year, during 2016 and 2017.
Case narrative interviews will include
follow up interviews. Interviews from
multiple perspectives will enhance the
government’s understanding of
strategies by which grantees can
identify, engage and serve diverse
populations of victims of severe forms
of human trafficking.
Respondents: Project directors and
case managers at the three FY 2015
FYSB funded demonstration projects;
staff (e.g., program managers and
directors) from partner organizations
that are working with the three FY 2015
FYSB-funded demonstration projects;
and clients who have received services
from the three FY 2015 FYSB-funded
demonstration projects.
ANNUAL BURDEN ESTIMATES
Total number
of respondents
Lhorne on DSK5TPTVN1PROD with NOTICES
Instrument
Project Director Interview .....................................................
Case Manger Interview ........................................................
Partner Interviews ................................................................
Case Narrative Interview .....................................................
Client Interview ....................................................................
Human Trafficking Evaluation Cost Module/Human Trafficking Evaluation Labor Module ......................................
Bi-monthly Project Director Calls .........................................
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Annual
number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Annual
burden hours
6
30
30
30
30
1
1
1
1
1
2
1.25
1.25
1
1
6
19
19
15
15
6
6
Fmt 4703
3
15
15
15
15
3
3
1
1
1
6
3
18
Sfmt 4703
E:\FR\FM\09MRN1.SGM
09MRN1
12498
Federal Register / Vol. 81, No. 46 / Wednesday, March 9, 2016 / Notices
Estimated total annual burden hours:
95.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 330
C Street SW., Washington, DC 20201,
Attn: OPRE Reports Clearance Officer.
All requests should be identified by the
title of the information collection. Email
address: OPREinfocollection@
acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect 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,
ACF Certifying Officer.
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
[FR Doc. 2016–05240 Filed 3–8–16; 8:45 am]
Written/Paper Submissions
BILLING CODE 4184–01–P
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Division of Dockets
Management, FDA will post your
comment, as well as any attachments,
except for information submitted,
marked and identified, as confidential,
if submitted as detailed in
‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2014–D–1180 for ‘‘Ensuring Safety of
Animal Feed Maintained and Fed OnFarm.’’ Received comments will be
placed in the docket and, except for
those submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Division of Dockets Management
between 9 a.m. and 4 p.m., Monday
through Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2014–D–1180]
Ensuring Safety of Animal Feed
Maintained and Fed On-Farm;
Guidance for Industry; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a
guidance for industry (GFI) # 203
entitled ‘‘Ensuring Safety of Animal
Feed Maintained and Fed On-Farm.’’
This guidance is intended to help
animal producers (persons who feed
animals) develop and implement onfarm practices to ensure the safety of
animal feed maintained and fed to
animals on the farm.
DATES: Submit either electronic or
written comments on Agency guidances
at any time.
ADDRESSES: You may submit comments
as follows:
Lhorne on DSK5TPTVN1PROD with NOTICES
SUMMARY:
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15:08 Mar 08, 2016
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with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ The
Agency will review this copy, including
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on https://
www.regulations.gov. Submit both
copies to the Division of Dockets
Management. If you do not wish your
name and contact information to be
made publicly available, you can
provide this information on the cover
sheet and not in the body of your
comments and you must identify this
information as ‘‘confidential.’’ Any
information marked as ‘‘confidential’’
will not be disclosed except in
accordance with 21 CFR 10.20 and other
applicable disclosure law. For more
information about FDA’s posting of
comments to public dockets, see 80 FR
56469, September 18, 2015, or access
the information at: https://www.fda.gov/
regulatoryinformation/dockets/
default.htm.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
Submit written requests for single
copies of the guidance to the Policy and
Regulations Staff (HFV–6), Center for
Veterinary Medicine, Food and Drug
Administration, 7519 Standish Pl.,
Rockville, MD 20855. Send one selfaddressed adhesive label to assist that
office in processing your requests. See
the SUPPLEMENTARY INFORMATION section
for electronic access to the guidance
document.
FOR FURTHER INFORMATION CONTACT:
Phares Okelo, Center for Veterinary
Medicine (HFV–226), Food and Drug
Administration, 7519 Standish Pl.,
Rockville, MD 20855, 240–402–5921,
email: phares.okelo@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of March 20,
2015 (80 FR 15014), FDA published the
notice of availability for a draft GFI #203
entitled ‘‘Ensuring Safety of Animal
Feed Maintained and Fed On-Farm’’
giving interested persons until June 3,
2015, to comment on the draft guidance.
FDA received several comments on the
E:\FR\FM\09MRN1.SGM
09MRN1
]]>Agencies
[Federal Register Volume 81, Number 46 (Wednesday, March 9, 2016)]
[Notices]
[Pages 12497-12498]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-05240]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Evaluation of Domestic Human Trafficking Demonstration
Projects.
OMB No.: New Collection.
Description: The Administration for Children and Families (ACF),
U.S. Department of Health and Human Services (HHS) is proposing a 2-
year data collection as part of the ``Evaluation of Domestic Human
Trafficking Demonstration Projects'' study. This notice addresses the
cross-site process evaluation to be conducted with the FY 2015 domestic
human trafficking demonstration sites funded by the Family and Youth
Services Bureau (FYSB).
The objective of the process evaluation is to describe program
operations and implementation experience, such as start-up efforts,
service provision to a wide array of trafficking victims, collaboration
development, training, and sustainability actions. Information from the
evaluation will assist federal, state, and community policymakers and
funders in laying the groundwork for the refinement of program models
to serve domestic victims of human trafficking, as well as evaluation
strategies for future programs targeting trafficking victims.
The evaluation of domestic human trafficking demonstration projects
will document and describe each site's community and organizational
capacity; partnership composition and functioning; comprehensive,
victim-centered services; and survivor characteristics, experiences,
and outcomes. Primary data for the evaluation will be collected via
qualitative interviews, including key informant interviews, case
narrative interviews, client interviews, bimonthly telephone
interviews, and cost modules (i.e., structured interviews with project
directors to collect information on costs). Data will be collected via
two site visits per year, during 2016 and 2017. Case narrative
interviews will include follow up interviews. Interviews from multiple
perspectives will enhance the government's understanding of strategies
by which grantees can identify, engage and serve diverse populations of
victims of severe forms of human trafficking.
Respondents: Project directors and case managers at the three FY
2015 FYSB funded demonstration projects; staff (e.g., program managers
and directors) from partner organizations that are working with the
three FY 2015 FYSB-funded demonstration projects; and clients who have
received services from the three FY 2015 FYSB-funded demonstration
projects.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Annual number Number of Average
Instrument Total number of responses per burden hours Annual burden
of respondents respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
Project Director Interview...... 6 3 1 2 6
Case Manger Interview........... 30 15 1 1.25 19
Partner Interviews.............. 30 15 1 1.25 19
Case Narrative Interview........ 30 15 1 1 15
Client Interview................ 30 15 1 1 15
Human Trafficking Evaluation 6 3 1 1 3
Cost Module/Human Trafficking
Evaluation Labor Module........
Bi-monthly Project Director 6 3 1 6 18
Calls..........................
----------------------------------------------------------------------------------------------------------------
[[Page 12498]]
Estimated total annual burden hours: 95.
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of Planning, Research and Evaluation, 330 C Street SW.,
Washington, DC 20201, Attn: OPRE Reports Clearance Officer. All
requests should be identified by the title of the information
collection. Email address: OPREinfocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect 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,
ACF Certifying Officer.
[FR Doc. 2016-05240 Filed 3-8-16; 8:45 am]
BILLING CODE 4184-01-P
