Proposed Collection: 60-Day Comment Request; Generic Clearance To Support the Safe to Sleep® Campaign at the Eunice Kennedy Shriver National Institute for Child Health and Human Development (NICHD), 40776-40777 [2017-18196]
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• This invention comprises a method
of treating HIV using therapeutics
geared toward viral release and entry,
distinguishing it from other antiviral
candidates with its method of action.
• CD62L is a new target for HIV
Development Stage
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Joseph Kononchik, NIAID, NIH
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Ruiping Wang, NIAID, NIH
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Dated: August 15, 2017.
Suzanne Frisbie,
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[FR Doc. 2017–18137 Filed 8–25–17; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: August 18, 2017.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
AGENCY:
[FR Doc. 2017–18197 Filed 8–25–17; 8:45 am]
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Federal Advisory Committee Act, as
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following meeting.
The meeting will be closed to the
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[FR Doc. 2017–18199 Filed 8–25–17; 8:45 am]
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National Institutes of Health
Proposed Collection: 60-Day Comment
Request; Generic Clearance To
Support the Safe to Sleep® Campaign
at the Eunice Kennedy Shriver National
Institute for Child Health and Human
Development (NICHD)
National Institutes of Health,
HHS.
ACTION:
Notice.
In compliance with the
requirement of the Paperwork
Reduction Act of 1995 to provide
opportunity for public comment on
proposed data collection projects, the
Eunice Kennedy Shriver National
Institute of Child Health and Human
Development (NICHD), the National
Institutes of Health (NIH) will publish
periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 60 days of the date of this
publication.
FOR FURTHER INFORMATION CONTACT: To
obtain a copy of the data collection
plans and instruments, submit
comments in writing, or request more
information on the proposed project,
contact: Lorena Kaplan, M.P.H., CHES,
Office of Communications, Eunice
Kennedy Shriver National Institute of
Child Health and Human Development,
National Institutes of Health, 31 Center
Drive, Room 2A32, Bethesda, Maryland
20892, or call non-toll free number (301)
496–6670 or Email your request,
including your address to
lorena.kaplan@nih.gov. Formal requests
for additional plans and instruments
must be requested in writing.
SUPPLEMENTARY INFORMATION: Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: Written
comments and/or suggestions from the
public and affected agencies are invited
to address one or more of the following
points: (1) Whether the proposed
collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information will have
practical utility; (2) the accuracy of the
agency’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
SUMMARY:
E:\FR\FM\28AUN1.SGM
28AUN1
40777
Federal Register / Vol. 82, No. 165 / Monday, August 28, 2017 / Notices
collected; and (4) ways to minimize the
burden of the collection of information
on those who are to respond, including
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology.
Proposed Collection Title: Generic
Clearance to Support the Safe to Sleep®
Campaign at the Eunice Kennedy
Shriver National Institute for Child
Health and Human Development
(NICHD), 0925–0701 Reinstatement
without Change Eunice Kennedy
Shriver National Institute of Child
Health and Human Development
(NICHD), National Institutes of Health
(NIH).
Need and Use of Information
Collection: This is a request to reinstate
without change a generic clearance that
would be used for submissions specific
to the Eunice Kennedy Shriver National
Institute of Child Health and Human
Development (NICHD) Safe to Sleep®
(STS) public education campaign.
Submissions for the STS campaign will
be used to assess the understanding and
reach of STS campaign materials and
messages, and to monitor and improve
campaign activities such as training
workshops and overall implementation.
The purpose of this information
collection is to monitor and modify
campaign activities, to plan future
campaign activities, to develop
messages and materials, and to develop
inform current campaign activities; and
(5) inform and/or change practices and
behaviors of program participants.
Examples of the types of information
collections that could be included under
this generic clearance include: Focus
groups and in-depth interviews with
parents/caregivers and/or health
professionals to get feedback on
distribution and outreach activities,
and/or campaign messages; and Surveys
with parents/caregivers and/or health
professionals to: (1) Assess the
usefulness of the new STS campaign
materials, including print and online
materials and a video, (2) track outreach
experiences of program participants, (3)
assess training participants’ changes in
knowledge related to safe infant sleep
behavior and implementation of
outreach methods taught, and (4) assess
program participants’ resource needs.
The sub-studies for this generic
clearance will be small scale, designed
to obtain results frequently and quickly
to guide campaign development and
implementation, inform campaign
direction, and be used internally for
campaign management purposes.
NICHD’s current scope and capacity for
STS generic sub-studies is non-existent
and this request would fill this gap.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
12,920.
distribution and outreach strategies that
are effective at communicating their
message to bring about the intended
response, awareness, and/or behavioral
change for the target audiences. This
generic clearance will enable the NICHD
to: (1) More efficiently assess the
implementation of campaign activities;
(2) better understand the target
audiences’ knowledge, attitudes, and
beliefs toward STS messages and
materials; (3) better understand how the
campaign activities have influenced the
target audiences’ behaviors and
practices; and (4) monitor and improve
activities such as trainings, materials,
and messages. Having a way to gather
feedback on the STS campaign activities
is critical to assessing the reach and
effect of campaign efforts. Data collected
for the campaign can inform where
future STS campaign resources can
produce the most meaningful results.
Data collected for the STS campaign
generic clearance will be used by a
number of audiences, including STS
campaign staff, NICHD leadership, STS
campaign collaborators, Federal SUID/
SIDS Workgroup members, SUID/SIDS
stakeholders, clinical and maternal and
child health professionals. These
audiences may use the information
collections to: (1) Develop new
campaign messages, materials, and/or
training curricula; (2) monitor and
improve campaign activities; (3) make
decisions about campaign activities; (4)
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden
per response
(in hours)
Focus Groups .......................................................
Interviews ..............................................................
Pre/Post Tests ......................................................
Pre/Post Tests ......................................................
Surveys .................................................................
Tracking/Feedback Form ......................................
General Public ..............
General Public ..............
General Public ..............
Health Professionals ....
Health Professionals ....
Health Educators ..........
45
45
3,500
20,000
2,000
40
1
1
2
2
1
2
1
1
15/60
15/60
30/60
1
45
45
1,750
10,000
1,000
80
Total ...............................................................
asabaliauskas on DSKBBXCHB2PROD with NOTICES
Type of
respondents
.......................................
25,630
49,170
........................
12,920
Dated: August 23, 2017.
Jennifer Guimond,
Project Clearance Liaison, Eunice Kennedy
Shriver National Institute of Child Health and
Human Development, National Institutes of
Health.
[FR Doc. 2017–18196 Filed 8–25–17; 8:45 am]
18:45 Aug 25, 2017
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center For Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
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VerDate Sep<11>2014
Number of
respondents
Number
of responses
per
respondent
Form name
Jkt 241001
PO 00000
Frm 00034
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Total annual
burden hours
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; PAR:
Development of Appropriate Pediatric
Formulations and Pediatric Drug Delivery
Systems.
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]]>Agencies
[Federal Register Volume 82, Number 165 (Monday, August 28, 2017)]
[Notices]
[Pages 40776-40777]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-18196]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection: 60-Day Comment Request; Generic Clearance To
Support the Safe to Sleep[supreg] Campaign at the Eunice Kennedy
Shriver National Institute for Child Health and Human Development
(NICHD)
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995 to provide opportunity for public comment on proposed data
collection projects, the Eunice Kennedy Shriver National Institute of
Child Health and Human Development (NICHD), the National Institutes of
Health (NIH) will publish periodic summaries of proposed projects to be
submitted to the Office of Management and Budget (OMB) for review and
approval.
DATES: Comments regarding this information collection are best assured
of having their full effect if received within 60 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data
collection plans and instruments, submit comments in writing, or
request more information on the proposed project, contact: Lorena
Kaplan, M.P.H., CHES, Office of Communications, Eunice Kennedy Shriver
National Institute of Child Health and Human Development, National
Institutes of Health, 31 Center Drive, Room 2A32, Bethesda, Maryland
20892, or call non-toll free number (301) 496-6670 or Email your
request, including your address to lorena.kaplan@nih.gov. Formal
requests for additional plans and instruments must be requested in
writing.
SUPPLEMENTARY INFORMATION: Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: Written comments and/or suggestions
from the public and affected agencies are invited to address one or
more of the following points: (1) Whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) the accuracy of the agency'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
[[Page 40777]]
collected; and (4) ways to minimize the burden of the collection of
information on those who are to respond, including the use of
appropriate automated, electronic, mechanical, or other technological
collection techniques or other forms of information technology.
Proposed Collection Title: Generic Clearance to Support the Safe to
Sleep[supreg] Campaign at the Eunice Kennedy Shriver National Institute
for Child Health and Human Development (NICHD), 0925-0701 Reinstatement
without Change Eunice Kennedy Shriver National Institute of Child
Health and Human Development (NICHD), National Institutes of Health
(NIH).
Need and Use of Information Collection: This is a request to
reinstate without change a generic clearance that would be used for
submissions specific to the Eunice Kennedy Shriver National Institute
of Child Health and Human Development (NICHD) Safe to Sleep[supreg]
(STS) public education campaign. Submissions for the STS campaign will
be used to assess the understanding and reach of STS campaign materials
and messages, and to monitor and improve campaign activities such as
training workshops and overall implementation. The purpose of this
information collection is to monitor and modify campaign activities, to
plan future campaign activities, to develop messages and materials, and
to develop distribution and outreach strategies that are effective at
communicating their message to bring about the intended response,
awareness, and/or behavioral change for the target audiences. This
generic clearance will enable the NICHD to: (1) More efficiently assess
the implementation of campaign activities; (2) better understand the
target audiences' knowledge, attitudes, and beliefs toward STS messages
and materials; (3) better understand how the campaign activities have
influenced the target audiences' behaviors and practices; and (4)
monitor and improve activities such as trainings, materials, and
messages. Having a way to gather feedback on the STS campaign
activities is critical to assessing the reach and effect of campaign
efforts. Data collected for the campaign can inform where future STS
campaign resources can produce the most meaningful results.
Data collected for the STS campaign generic clearance will be used
by a number of audiences, including STS campaign staff, NICHD
leadership, STS campaign collaborators, Federal SUID/SIDS Workgroup
members, SUID/SIDS stakeholders, clinical and maternal and child health
professionals. These audiences may use the information collections to:
(1) Develop new campaign messages, materials, and/or training
curricula; (2) monitor and improve campaign activities; (3) make
decisions about campaign activities; (4) inform current campaign
activities; and (5) inform and/or change practices and behaviors of
program participants.
Examples of the types of information collections that could be
included under this generic clearance include: Focus groups and in-
depth interviews with parents/caregivers and/or health professionals to
get feedback on distribution and outreach activities, and/or campaign
messages; and Surveys with parents/caregivers and/or health
professionals to: (1) Assess the usefulness of the new STS campaign
materials, including print and online materials and a video, (2) track
outreach experiences of program participants, (3) assess training
participants' changes in knowledge related to safe infant sleep
behavior and implementation of outreach methods taught, and (4) assess
program participants' resource needs.
The sub-studies for this generic clearance will be small scale,
designed to obtain results frequently and quickly to guide campaign
development and implementation, inform campaign direction, and be used
internally for campaign management purposes. NICHD's current scope and
capacity for STS generic sub-studies is non-existent and this request
would fill this gap.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 12,920.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Type of Number of Number of burden per Total annual
Form name respondents respondents responses per response (in burden hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Focus Groups.................. General Public.. 45 1 1 45
Interviews.................... General Public.. 45 1 1 45
Pre/Post Tests................ General Public.. 3,500 2 15/60 1,750
Pre/Post Tests................ Health 20,000 2 15/60 10,000
Professionals.
Surveys....................... Health 2,000 1 30/60 1,000
Professionals.
Tracking/Feedback Form........ Health Educators 40 2 1 80
---------------------------------------------------------------
Total..................... ................ 25,630 49,170 .............. 12,920
----------------------------------------------------------------------------------------------------------------
Dated: August 23, 2017.
Jennifer Guimond,
Project Clearance Liaison, Eunice Kennedy Shriver National Institute of
Child Health and Human Development, National Institutes of Health.
[FR Doc. 2017-18196 Filed 8-25-17; 8:45 am]
BILLING CODE 4140-01-P
