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]

Download as PDF 40776 Federal Register / Vol. 82, No. 165 / Monday, August 28, 2017 / Notices Competitive Advantages • 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 • In vitro studies; Proof-of-concept studies. Inventors Peter Sun, NIAID, NIH Joseph Kononchik, NIAID, NIH Joanna Ireland, NIAID, NIH Ruiping Wang, NIAID, NIH Intellectual Property: HHS Reference No. E–261–2015/0—PCT No. PCT/ US2016/068713 filed 12/27/2016. Licensing Contact: Chris Kornak, 240– 627–3705, Chris.Kornak@nih.gov. Collaborative Research Opportunity: The Technology Transfer and Intellectual Property Office (TTIPO) is seeking parties interested in collaborative research to further codevelop this technology by identifying pharmacological compounds inhibiting CD62L shedding by using high throughput compound screening. For collaboration opportunities, please contact Chris Kornak, 240–627–3705, Chris.Kornak@nih.gov. Dated: August 15, 2017. Suzanne Frisbie, Deputy Director, Technology Transfer and Intellectual Property Office, National Institute of Allergy and Infectious Diseases. [FR Doc. 2017–18137 Filed 8–25–17; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health asabaliauskas on DSKBBXCHB2PROD with NOTICES Office of the Director; Notice of Charter Renewal It is determined that the Advisory Committee to the Deputy Director for Intramural Research, National Institutes of Health, is in the public interest in connection with the performance of duties imposed on the National Institutes of Health by law, and that these duties can best be performed through the advice and counsel of this group. In accordance with Title 41 of the U.S. Code of Federal Regulations, Section 102–3.65(a), notice is hereby given that the Charter for the Advisory Committee to the Deputy Director for Intramural Research, National Institutes of Health, was renewed for an VerDate Sep<11>2014 18:45 Aug 25, 2017 Jkt 241001 additional two-year period on August 15, 2017. Inquiries may be directed to Jennifer Spaeth, Director, Office of Federal Advisory Committee Policy, Office of the Director, National Institutes of Health, 6701 Democracy Boulevard, Suite 1000, Bethesda, Maryland 20892 (Mail code 4875), Telephone (301) 496– 2123, or spaethj@od.nih.gov. 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] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Aging; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 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: National Institute on Aging Initial Review Group; Behavior and Social Science of Aging Review Committee. Date: October 5–6, 2017. Time: 3:00 p.m. to 2:00 p.m. Agenda: To review and evaluate grant applications. Place: Bethesda Marriott, 5151 Pooks Hill Road, Bethesda, MD 20814. Contact Person: Kimberly Firth, Ph.D., National Institute on Aging, Gateway Building, 7201 Wisconsin Avenue, Suite 2C212, Bethesda, MD 20892, 301–402–7702, kimberly.firth@nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.866, Aging Research, National Institutes of Health, HHS) Dated: August 23, 2017. Melanie J. Pantoja, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2017–18199 Filed 8–25–17; 8:45 am] BILLING CODE 4140–01–P PO 00000 Frm 00033 Fmt 4703 Sfmt 4703 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 BILLING CODE 4140–01–P VerDate Sep<11>2014 Number of respondents Number of responses per respondent Form name Jkt 241001 PO 00000 Frm 00034 Fmt 4703 Sfmt 4703 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. E:\FR\FM\28AUN1.SGM 28AUN1

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]


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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