30-day FRN

Federal Register / Vol. 82, No. 216 / Thursday, November 9, 2017 / Notices
Dated: October 15, 2017.
Celia Wolfman,
Project Clearance Liaison, FIC, NIH.
[FR Doc. 2017–24362 Filed 11–8–17; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request; Generic Clearance
To Support the Safe To Sleep®
Campaign (Eunice Kennedy Shriver
National Institute of Child Health and
Human Development)
AGENCY:

National Institutes of Health,

HHS.
ACTION:

Notice.

In compliance with the
Paperwork Reduction Act of 1995, the
National Institutes of Health (NIH) has
submitted to the Office of Management
and Budget (OMB) a request for review
and approval of the information
collection listed below.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 30-days of the date of this
publication.
ADDRESSES: Written comments and/or
suggestions regarding the item(s)
contained in this notice, especially
regarding the estimated public burden
and associated response time, should be
directed to the: Office of Management
and Budget, Office of Regulatory Affairs,
[email protected] or by
fax to 202–395–6974, Attention: Desk
Officer for NIH.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, 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
[email protected]. Formal requests
for additional plans and instruments
must be requested in writing.
SUPPLEMENTARY INFORMATION: This
proposed information collection was
previously published in the Federal
Register on Monday, August 28, 2017,

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SUMMARY:

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page 40776–40777 (82 FR 40776–40777)
and allowed 60 days for public
comment. NICHD received one
comment in response to the 60-Day
Federal Register Notice. The purpose of
this notice is to allow an additional 30
days for public comment.
The Eunice Kennedy Shriver National
Institute of Child Health and Human
Development (NICHD), National
Institutes of Health, may not conduct or
sponsor, and the respondent is not
required to respond to, an information
collection that has been extended,
revised, or implemented on or after
October 1, 1995, unless it displays a
currently valid OMB control number.
In compliance with section
3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Institutes of Health (NIH) has submitted
to the Office of Management and Budget
(OMB) a request for review and
approval of the information collection
listed below.
Proposed Collection: Generic
Clearance to Support the Safe to Sleep®
Campaign 0925–0701,
REINSTATEMENT WITH CHANGE at
the Eunice Kennedy Shriver National
Institute for Child Health and Human
Development (NICHD), National
Institutes of Health (NIH).
Need and Use of Information
Collection: This is a request to reinstate
with 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
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

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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 on-line
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.
Changes have been made to the
annualized burden hours to reflect the
anticipated data collections during the
next 3 years.
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.

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Federal Register / Vol. 82, No. 216 / Thursday, November 9, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses
per
respondent

Average
burden per
response
(in hours)

Total annual
burden hours

Type of respondents

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 ...........................................

...........................................................

25,630

49,170

........................

12,920

Dated: November 2, 2017.
Jennifer Guimond,
Project Clearance Liaison, Eunice Kennedy
Shriver National Institute of Child Health and
Human Development, National Institutes of
Health.
[FR Doc. 2017–24399 Filed 11–8–17; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Toxicology Program Board of
Scientific Counselors; Announcement
of Meeting; Request for Comments
AGENCY:

National Institutes of Health,

HHS.
ACTION:

Notice.

This notice announces the
next meeting of the National Toxicology
Program (NTP) Board of Scientific
Counselors (BSC). The BSC, a federally
chartered, external advisory group
composed of scientists from the public
and private sectors, will review and
provide advice on programmatic
activities. The meeting is open to the
public and registration is requested for
both attendance and oral comment and
required to access the webcast.
Information about the meeting and
registration are available at http://
ntp.niehs.nih.gov/go/165.
DATES:
Meeting: December 7–8, 2017; Day
one begins at 8:30 a.m. Eastern Standard
Time (EST) and ends at approximately
5:00 p.m. Day 2 begins at 8:30 a.m. and
continues until adjournment.
Written Public Comment
Submissions: Deadline is November 30,
2017.
Oral Comments: Deadline is
November 30, 2017.
Registration for Meeting: Deadline
December 8, 2017.
Registration to view the meeting via
the webcast is required.
ADDRESSES:
SUMMARY:

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Number of
respondents

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Meeting Location: Rodbell
Auditorium, Rall Building, National
Institute of Environmental Health
Sciences (NIEHS), 111 T.W. Alexander
Drive, Research Triangle Park, NC
27709.
Meeting Web page: The preliminary
agenda, registration, and other meeting
materials are at http://ntp.niehs.nih.gov/
go/165.
Webcast: The meeting will be
webcast; the URL will be provided to
those who register for viewing.
FOR FURTHER INFORMATION CONTACT: Dr.
Mary Wolfe, Designated Federal Officer
for the BSC, Office of Liaison, Policy
and Review, Division of NTP, NIEHS,
P.O. Box 12233, K2–03, Research
Triangle Park, NC 27709. Phone: 984–
287–3209, Fax: 301–451–5759, Email:
[email protected]. Hand Deliver/
Courier address: 530 Davis Drive, Room
K2130, Morrisville, NC 27560.
SUPPLEMENTARY INFORMATION:
Meeting and Registration: The
meeting is open to the public with time
scheduled for oral public comments;
attendance at the meeting is limited
only by the space available. The BSC
will provide input to the NTP on
programmatic activities and issues.
Preliminary agenda topics include: US
Strategic Roadmap: New Approaches to
Evaluate the Safety of Chemicals and
Medical Products; NTP Assessing
Alternative Approaches; New
Approaches to Hazard Characterization
and Risk Assessment; Update on NTP
Studies of Glyphosate; and Report on
Peer Review of Draft Report on
Carcinogens Monograph on Haloacetic
Acids. Please see the preliminary
agenda for information about the
specific presentations. The preliminary
agenda, roster of BSC members,
background materials, public comments,
and any additional information, when
available, will be posted on the BSC
meeting Web site (http://
ntp.niehs.nih.gov/go/165) or may be
requested in hardcopy from the
Designated Federal Official for the BSC.
Following the meeting, summary

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minutes will be prepared and made
available on the BSC meeting Web site.
The public may attend the meeting in
person or view the webcast. Registration
is required to view the webcast; the URL
for the webcast will be provided in the
email confirming registration.
Individuals who plan to provide oral
comments (see below) are encouraged to
register online at the BSC meeting Web
site (http://ntp.niehs.nih.gov/go/165) by
November 30, 2017, to facilitate
planning for the meeting. Individuals
are encouraged to access the Web site to
stay abreast of the most current
information regarding the meeting.
Visitor and security information for
those attending in-person is available at
niehs.nih.gov/about/visiting/index.cfm.
Individuals with disabilities who need
accommodation to participate in this
event should contact Ms. Robbin Guy at
phone: (984) 287–3136 or email: guyr2@
niehs.nih.gov. TTY users should contact
the Federal TTY Relay Service at 800–
877–8339. Requests should be made at
least five business days in advance of
the event.
Request for Comments: Written
comments submitted in response to this
notice should be received by November
30, 2017. Comments will be posted on
the BSC meeting Web site and persons
submitting them will be identified by
their name and affiliation and/or
sponsoring organization, if applicable.
Persons submitting written comments
should include their name, affiliation (if
applicable), phone, email, and
sponsoring organization (if any) with
the document. Guidelines for public
comments are at http://
ntp.niehs.nih.gov/ntp/about_ntp/
guidelines_public_comments_508.pdf.
Time is allotted during the meeting
for the public to present oral comments
to the BSC on the agenda topics. Public
comments can be presented in-person at
the meeting or by teleconference line.
There are 50 lines for this call;
availability is on a first-come, firstserved basis. The lines will be open
from 8:30 a.m. until adjournment,

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