Submission for OMB Review; Comment Request, 57758-57759 [2017-26353]
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57758
Federal Register / Vol. 82, No. 234 / Thursday, December 7, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
respondents
Type of respondents
Form name
Treatment facility staff .....................................
Client Questionnaire Baseline ........................
Client Questionnaire 12-Month Follow-up .....
Client Questionnaire 24-Month Follow-up .....
Client Focus Groups ......................................
Staff Focus Groups ........................................
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2017–26399 Filed 12–6–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket Number CDC–2017–0104, NIOSH–
304]
Draft—National Occupational Research
Agenda for Traumatic Injury
Prevention
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Request for comment.
AGENCY:
The National Institute for
Occupational Safety and Health of the
Centers for Disease Control and
Prevention announces the availability of
a draft NORA Agenda entitled National
Occupational Research Agenda for
Traumatic Injury Prevention for public
comment. To view the notice and
related materials, visit https://
www.regulations.gov. and enter CDC–
2017–0104 in the search field and click
‘‘Search.’’
SUMMARY:
sradovich on DSK3GMQ082PROD with NOTICES
Table of Contents
•
•
•
•
•
Dates
Addresses
For Further Information Contact
Supplementary Information
Background
Electronic or written comments
must be received by February 5, 2018.
ADDRESSES: You may submit comments,
identified by CDC–2017–0104 and
docket number NIOSH–304, by any of
the following methods:
DATES:
VerDate Sep<11>2014
18:50 Dec 06, 2017
Jkt 244001
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: National Institute for
Occupational Safety and Health, NIOSH
Docket Office, 1090 Tusculum Avenue,
MS C–34, Cincinnati, Ohio 45226–1998.
Instructions: All submissions received
in response to this notice must include
the agency name and docket number
[CDC–2017–0104; NIOSH–304]. All
relevant comments received will be
posted without change to https://
www.regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
https://www.regulations.gov. All
information received in response to this
notice will also be available for public
examination and copying at the NIOSH
Docket Office, 1150 Tusculum Avenue,
Room 155, Cincinnati, OH 45226–1998.
FOR FURTHER INFORMATION CONTACT:
Emily Novicki (NORACoordinator@
cdc.gov), National Institute for
Occupational Safety and Health, Centers
for Disease Control and Prevention,
Mailstop E–20, 1600 Clifton Road NE.,
Atlanta, GA 30329, phone (404) 498–
2581 (not a toll free number).
SUPPLEMENTARY INFORMATION: The
National Occupational Research Agenda
(NORA) is a partnership program
created to stimulate innovative research
and improved workplace practices. The
national agenda is developed and
implemented through the NORA sector
and cross-sector councils. Each council
develops and maintains an agenda for
its sector or cross-sector.
Background: The National
Occupational Research Agenda for
Traumatic Injury Prevention (the
Agenda) is intended to identify the
research, information, and actions most
urgently needed to prevent occupational
traumatic injuries. The National
Occupational Research Agenda for
Traumatic Injury Prevention provides a
vehicle for industry stakeholders to
describe the most relevant issues, gaps,
and safety and health needs for the
cross-sector. Each NORA research
agenda is meant to guide or promote
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Number of
responses per
respondent
1,187
930
744
27
27
Average
burden per
response
(in hours)
1
1
1
1
1
52/60
45/60
45/60
90/60
90/60
high priority research efforts on a
national level, conducted by various
entities, including government, higher
education, and the private sector.
This is the first Traumatic Injury
Prevention Agenda, developed for the
third decade of NORA (2016–2026). The
Agenda was developed considering
information about injuries, the state of
the science, and the probability that
new information and approaches will
make a difference.
As the steward of the NORA process,
NIOSH invites comments on the draft
National Occupational Research
Agenda for Traumatic Injury
Prevention. Comments expressing
support or with specific
recommendations to improve the
Agenda are requested. A copy of the
draft Agenda is available at https://
www.regulations.gov (search Docket
Number CDC–2017–0104).
Frank Hearl,
Chief of Staff, National Institute for
Occupational Safety and Health, Centers for
Disease Control and Prevention.
[FR Doc. 2017–26359 Filed 12–6–17; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Annual Statistical Report on
Children in Foster Homes and Children
in Families Receiving Payment in
Excess of the Poverty Income Level from
a State Program Funded under Part A of
Title IV of the Social Security Act.
OMB No.: 0970–0004.
Description: The Department of
Health and Human Services is required
to collect these data under section 1124
of Title I of the Elementary and
Secondary Education Act of 1965, as
amended by Public Law 114–95. The
data are used by the U.S. Department of
Education for allocation of funds for
programs to aid disadvantaged
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Federal Register / Vol. 82, No. 234 / Thursday, December 7, 2017 / Notices
elementary and secondary students.
Respondents include various
components of State Human Service
agencies.
Respondents: The 52 respondents
include the 50 States, the District of
Columbia, and Puerto Rico.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Annual Statistical Report on Children in Foster Homes and Children Receiving Payments in Excess of the Poverty Level From a State Program
Funded Under Part A of Title IV of the Social Security Act ........................
Estimated Total Annual Burden
Hours: 13,746.20.
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.
Attention Reports Clearance Officer. All
requests should be identified by the title
of the information collection. Email
address: infocollection@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,
Reports Clearance Officer.
Food and Drug Administration
[Docket No. FDA–2017–N–6476]
sradovich on DSK3GMQ082PROD with NOTICES
Pediatric Rare Diseases—A
Collaborative Approach for Drug
Development Using Gaucher Disease
as a Model; Draft Guidance for
Industry; Availability
Food and Drug Administration,
HHS.
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry entitled ‘‘Pediatric
SUMMARY:
VerDate Sep<11>2014
18:50 Dec 06, 2017
Submit either electronic or
written comments on the draft guidance
by February 5, 2018 to ensure that the
Agency considers your comment on this
draft guidance before it begins work on
the final version of the guidance.
DATES:
Electronic Submissions
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
ACTION:
Rare Diseases—A Collaborative
Approach for Drug Development Using
Gaucher Disease as a Model.’’ This draft
guidance focuses on drug development
for pediatric patients with Gaucher
disease. In particular, it proposes for
consideration a novel approach to
improve the efficiency of drug
development in pediatric rare diseases
using Gaucher disease as an example.
The emergence of concomitant trials for
multiple investigational drug products
for the treatment of rare diseases can
pose significant challenges to effective
drug development, because there are
limited numbers of patients for any
given rare condition worldwide. This
approach discusses the feasibility of the
development of multiple drug products
in a time-efficient manner while
minimizing the number of patients
necessary to be treated with placebo.
You may submit comments
on any guidance at any time as follows:
BILLING CODE 4184–01–P
AGENCY:
52
ADDRESSES:
[FR Doc. 2017–26353 Filed 12–6–17; 8:45 am]
Jkt 244001
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
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Number of
responses per
respondent
1
Average
burden hours
per response
264.35
Total burden
hours
13,746.20
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’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, 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–
2017–N–6476 for ‘‘Pediatric Rare
Diseases—A Collaborative Approach for
Drug Development Using Gaucher
Disease as a Model; Draft Guidance for
Industry; Availability’’. 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 Dockets Management Staff
office 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
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
E:\FR\FM\07DEN1.SGM
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Agencies
[Federal Register Volume 82, Number 234 (Thursday, December 7, 2017)]
[Notices]
[Pages 57758-57759]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-26353]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Annual Statistical Report on Children in Foster Homes and
Children in Families Receiving Payment in Excess of the Poverty Income
Level from a State Program Funded under Part A of Title IV of the
Social Security Act.
OMB No.: 0970-0004.
Description: The Department of Health and Human Services is
required to collect these data under section 1124 of Title I of the
Elementary and Secondary Education Act of 1965, as amended by Public
Law 114-95. The data are used by the U.S. Department of Education for
allocation of funds for programs to aid disadvantaged
[[Page 57759]]
elementary and secondary students. Respondents include various
components of State Human Service agencies.
Respondents: The 52 respondents include the 50 States, the District
of Columbia, and Puerto Rico.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Annual Statistical Report on Children in Foster 52 1 264.35 13,746.20
Homes and Children Receiving Payments in Excess
of the Poverty Level From a State Program
Funded Under Part A of Title IV of the Social
Security Act...................................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 13,746.20.
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. Attention Reports Clearance Officer. All requests
should be identified by the title of the information collection. Email
address: infocollection@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,
Reports Clearance Officer.
[FR Doc. 2017-26353 Filed 12-6-17; 8:45 am]
BILLING CODE 4184-01-P