Proposed Information Collection Activity; Comment Request, 10492-10493 [2015-03924]
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10492
Federal Register / Vol. 80, No. 38 / Thursday, February 26, 2015 / Notices
II. Public Meeting: NIOSH will hold a
public meeting to allow for comments
on future directions for surveillance of
injuries within the agricultural
production industry. The meeting is
open to the public, limited only by the
capacity of 100 connections to the Web
based conference.
Confirm your attendance to this
meeting by sending an email to
mgoldcamp@cdc.gov by March 16,
2015. An email confirming registration
will be sent from NIOSH and will
include details needed to participate.
Requests to make presentations at the
public meeting should be emailed to
mgoldcamp@cdc.gov by March 16,
2015. All requests to present should
contain the name, address, telephone
number, and relevant business
affiliations of the presenter. Presenters
will be assigned a 10-minute slot on the
agenda. Presenters who wish to use
slides must email an electronic file in
Microsoft PowerPoint format to
mgoldcamp@cdc.gov by March 16,
2015. An email confirming the
presentation request will be sent from
NIOSH and will include details needed
to present and an approximate start time
for the presentation.
If a presenter is not in attendance
when his/her presentation is scheduled
to begin, the remaining presenters will
be heard in order. After the last
scheduled presenter is heard, those who
missed their opportunity may be
allowed to present, limited by time
available.
Attendees who wish to speak, but did
not submit a request for the opportunity
to make a presentation, may be given
this opportunity after the scheduled
presenters are heard, at the discretion of
the presiding officer and limited by time
available.
The public meeting, including all
presentations and slides, will be
recorded, transcribed, and posted
without change to https://
www.regulations.gov, including any
personal information provided.
III. Written Comments: You may
submit comments, identified by CDC–
2015–0005 and Docket Number NIOSH–
281, by either of the following methods:
• 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.
All information received in response
to this notice must include the agency
name and docket number [CDC–2015–
0005; NIOSH–281]. All relevant
comments received will be posted
without change to https://
www.regulations.gov, including any
personal information provided. All
electronic comments should be
formatted as Microsoft Word. 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, Ohio 45226–
1998.
Dated: February 18, 2015.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2015–03949 Filed 2–25–15; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Youth Education and
Relationship Services (YEARS)
Descriptive Study.
OMB No.: New Collection.
Description: Since 2006, Congress has
authorized dedicated funding (currently
at the level of $75 million annually) to
support programs promoting healthy
marriage and relationship education
(HMRE). In order to better understand
the services that federally-funded HMRE
programs are providing to youth and the
populations the programs are reaching,
The Office of Planning, Research and
Evaluation (OPRE), within ACF/HHS is
proposing data collection activity as
part of the Youth Education and
Relationship Services (YEARS)
Descriptive Study. The data that ACF
proposes to collect includes information
on funding spent serving youth, the
number of youth being served, youth
demographic characteristics,
characteristics of the organizations or
programs serving youth, information on
program curricula and contents, and
program implementation information.
This data is to be collected through a
web-based survey that is to be
completed by HMRE grantee program
staff. This information will be critical to
informing future efforts to improve
HMRE programs serving youth.
Respondents: Healthy marriage and
relationship education (HMRE) grantee
program staff.
ANNUAL BURDEN ESTIMATES
Total number
of respondents
Annual
number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Annual burden
hours
Web-based survey ...............................................................
rmajette on DSK2VPTVN1PROD with NOTICES
Instrument
176
88
1
0.5
44
Estimated Total Annual Burden
Hours: 44
In compliance with the requirements
of Section 3506(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
VerDate Sep<11>2014
15:27 Feb 25, 2015
Jkt 235001
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: OPRE Reports Clearance Officer.
Email address: OPREinfocollection@
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 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
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Fmt 4703
Sfmt 4703
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.
Reference
[1] https://www.ssa.gov/OP_Home/ssact/
E:\FR\FM\26FEN1.SGM
26FEN1
Federal Register / Vol. 80, No. 38 / Thursday, February 26, 2015 / Notices
title04/0403.htm.
Karl Koerper,
Reports Clearance Officer.
[FR Doc. 2015–03924 Filed 2–25–15; 8:45 am]
BILLING CODE 4184–73–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–20115–N–0456]
Pediatric Stakeholder Meeting;
Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice of public meeting;
request for comments.
ACTION:
The Food and Drug
Administration’s (FDA) Office of
Pediatric Therapeutics (OPT), the Center
for Drug Evaluation and Research
(CDER) and the Center for Biologics
Evaluation and Research (CBER) are
announcing a public meeting seeking
input from patient groups, consumer
groups, regulated industry, academia
and other interested parties to obtain
any recommendations or information
relevant to the report to Congress that
FDA is required to submit concerning
pediatrics, as outlined in section 508 of
the Food and Drug Administration
Safety and Innovation Act (FDASIA)
(see the SUPPLEMENTARY INFORMATION
section for additional background
information).
DATES: The public meeting will be held
on March 25, 2015, from 9 a.m. to 5 p.m.
Registration to attend the meeting
should be received by March 20, 2015
(see the SUPPLEMENTARY INFORMATION
section for instructions).
ADDRESSES: The meeting will be held at
FDA’s White Oak Campus, 10903 New
Hampshire Ave., Building 31
Conference Center, the Great Room
(1503–B & C), Silver Spring, MD 20993–
0002. Entrance for the public meeting
participants (non-FDA employees) is
through Building 1 where routine
security check procedures will be
performed. For information on parking
and security procedures, please refer to
https://www.fda.gov/AboutFDA/
WorkingatFDA/BuildingsandFacilities/
WhiteOakCampusInformation/
ucm241740.
Submit either electronic or written
comments by April 24, 2015. Submit
electronic comments to https://
www.regulations.gov. Submit written
comments to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
rmajette on DSK2VPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
15:27 Feb 25, 2015
Jkt 235001
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FDA will post the agenda
approximately 5 days before the meeting
at: https://wwww.fda.gov/NewsEvents/
MeetingsConferencesWorkshops/
ucm433552.htm.
FOR FURTHER INFORMATION CONTACT:
Terrie L. Crescenzi, Office of Pediatric
Therapeutics, Food and Drug
Administration, 10903 New Hampshire
Ave., Silver Spring, MD 20993–0002,
terrie.crescenzi@fda.hhs.gov or Betsy
Sanford, Office of Pediatric
Therapeutics, Food and Drug
Administration, 10903 New Hampshire
Ave., Silver Spring, MD 20993–0002,
elizabeth.sanford@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On July 9, 2012, the President signed
into law the Food and Drug
Administration Safety and Innovation
Act (FDASIA) (Pub. L. 112–144).
Section 508 of FDASIA directs the
Secretary of HHS to submit a report to
Congress on the implementation of the
Best Pharmaceuticals for Children Act
(BPCA) and Pediatric Research Equity
Act (PREA). The first report must be
submitted to Congress by July 9, 2016,
and every 5 years thereafter. FDASIA
also requires FDA to obtain, at least 180
days prior to submission of the report,
stakeholder input from patient groups,
consumer groups, regulated industry,
academia, and any other interested
parties to obtain any recommendations
or information relevant to the report
including suggestions for modifications
that would improve pediatric drug
research and pediatric labeling of drugs
and biological products.
The basic content of the report will
include: An assessment of the
effectiveness of BPCA (section 505A)
and PREA (section 505B) in improving
information about pediatric uses for
approved drugs and biological products,
including the number and type of
labeling changes made since the
enactment of FDASIA and the
importance of such uses in the
improvement of the health of children;
various statistics related to both PREA
and BPCA, including the Written
Request referral process with the
National Institutes of Health; an
assessment of the timeliness and
effectiveness of pediatric study plans;
an assessment of studying biologics;
efforts made to increase the number of
studies conducted in the neonatal
population; the number and importance
of drugs and biologics studied in
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10493
children with cancer and any
recommendations for modification to
the programs that would improve
pediatric drug research and increase
labeling of drugs and biologics; an
assessment of the successes of and
limitations to studying drugs for rare
diseases; an assessment of the efforts to
address the suggestions and options
described in any prior report issued by
the Comptroller General, Institute of
Medicine, or the Secretary, and any
stakeholder recommendations or
modifications that would improve
pediatric drug research and pediatric
labeling of drugs and biological
products.
The specific topics to be discussed at
the meeting will include, but not be
limited to, pediatric labeling changes,
waivers and deferrals, Written Requests,
pediatric study plans, programmatic
activities with the NIH Written Request
referral process, activities concerning
neonates, pediatric cancers and rare
diseases, and transparency.
II. Meeting Attendance and
Participation
If you wish to attend this meeting,
visit https://
stakeholderinput.eventbrite.com. Please
register by March 20, 2015. Those who
are unable to attend the meeting in
person can register to view a live
Webcast of the meeting. You will be
asked to indicate in your registration if
you plan to attend in person or via the
Webcast. Your registration will also
contain your complete contact
information, including name, title,
affiliation, address, email address, and
phone number. Seating will be limited
so early registration is recommended.
Registration is free and will be on a firstcome, first-served basis. Onsite
registration on the day of the meeting
will be based on space availability. If
you need special accommodations due
to a disability, please contact Betsy
Sanford (see FOR FURTHER INFORMATION
CONTACT) at least 7 days in advance.
Persons attending the meeting are
advised that FDA is not responsible for
providing access to electrical outlets.
Persons interested in presenting
comments at the meeting will be asked
to indicate this in their registration.
FDA will try to accommodate all
participant requests to speak, however
the duration of comments may be
limited by time constraints.
Comments: Regardless of attendance
at the public meeting, you can submit
electronic or written comments to the
public docket (see ADDRESSES) by April
24, 2015. Received comments may be
seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
E:\FR\FM\26FEN1.SGM
26FEN1
]]>Agencies
[Federal Register Volume 80, Number 38 (Thursday, February 26, 2015)]
[Notices]
[Pages 10492-10493]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-03924]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Title: Youth Education and Relationship Services (YEARS)
Descriptive Study.
OMB No.: New Collection.
Description: Since 2006, Congress has authorized dedicated funding
(currently at the level of $75 million annually) to support programs
promoting healthy marriage and relationship education (HMRE). In order
to better understand the services that federally-funded HMRE programs
are providing to youth and the populations the programs are reaching,
The Office of Planning, Research and Evaluation (OPRE), within ACF/HHS
is proposing data collection activity as part of the Youth Education
and Relationship Services (YEARS) Descriptive Study. The data that ACF
proposes to collect includes information on funding spent serving
youth, the number of youth being served, youth demographic
characteristics, characteristics of the organizations or programs
serving youth, information on program curricula and contents, and
program implementation information. This data is to be collected
through a web-based survey that is to be completed by HMRE grantee
program staff. This information will be critical to informing future
efforts to improve HMRE programs serving youth.
Respondents: Healthy marriage and relationship education (HMRE)
grantee program staff.
Annual Burden Estimates
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Total number of Annual number responses per hours per Annual burden
respondents of respondents respondent response hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Web-based survey................................................... 176 88 1 0.5 44
--------------------------------------------------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 44
In compliance with the requirements of Section 3506(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: OPRE Reports Clearance Officer. Email
address: OPREinfocollection@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 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.
Reference
[1] https://www.ssa.gov/OP_Home/ssact/
[[Page 10493]]
title04/0403.htm.
Karl Koerper,
Reports Clearance Officer.
[FR Doc. 2015-03924 Filed 2-25-15; 8:45 am]
BILLING CODE 4184-73-P
