Published 30-Day FRN

Federal Register / Vol. 81, No. 103 / Friday, May 27, 2016 / Notices
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846– 93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: May 23, 2016.
Sylvia L. Neal,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–12499 Filed 5–26–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings

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Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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
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; Member
Conflict: Bioengineering Sciences.
Date: June 21, 2016.
Time: 2:00 p.m. to 5:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Joseph Thomas Peterson,
Ph.D., Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4118,
MSC 7814, Bethesda, MD 20892, 301–408–
9694, petersonjt@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Health Care Delivery and
Methodologies Research Project Grants.
Date: June 21, 2016.
Time: 2:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Jacinta Bronte-Tinkew,
Ph.D., Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3164,
MSC 7770, Bethesda, MD 20892, (301) 806–
0009, brontetinkewjm@csr.nih.gov.

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Name of Committee: Center for Scientific
Review Special Emphasis Panel; PAR Panel:
Temporal Dynamics of Neurophysiological
Patterns as Potential Targets for Treating
Cognitive Deficits in Brain Disorders.
Date: June 23, 2016.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Kirk Thompson, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5184,
MSC 7844, Bethesda, MD 20892, 301–435–
1242, kgt@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; AREA:
Applications in Cell and Developmental
Biology.
Date: June 23, 2016.
Time: 11:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Virtual Meeting).
Contact Person: Thomas Beres, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Dr., Rm. 5201, MSC
7840, Bethesda, MD 20892, 301–435–1175,
berestm@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; AREA:
Immunology.
Date: June 24, 2016.
Time: 10:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hilton Washington/Rockville, 1750
Rockville Pike, Rockville, MD 20852.
Contact Person: Alok Mulky, Ph.D.,
Scientific Review Officer, Center for
Scientific Review (CSR), National Institutes
of Health (NIH), 6701 Rockledge Dr., Room
4203, Bethesda, MD 20817, (301) 435–3566,
alok.mulky@nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: May 20, 2016.
Anna Snouffer,
Deputy Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2016–12506 Filed 5–26–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request a Generic
Submission for Formative Research,
Pretesting and Customer Satisfaction
of NCI’s Communication and
Education Resources (NCI)
Under the provisions of
section 3507(a)(1)(D) of the Paperwork
Reduction Act of 1995, the National
Cancer Institute, the National Institutes
of Health, has submitted to the Office of
Management and Budget (OMB) a
request for review and approval of the
information collection listed below.
This proposed information collection
was previously published in the Federal
Register on March 9, 2016 P. 12514 and
allowed 60 days for public comment. No
public comments were received. The
purpose of this notice is to allow an
additional 30 days for public comment.
The National Cancer Institute, NCI,
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.
Direct Comments To OMB: 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, OIRA_submission@
omb.eop.gov or by fax to 202–395–6974,
Attention: NIH Desk Officer.
Comment Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 30 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To
obtain a copy of the data collection
plans and instruments, or request more
information on the proposed project,
contact: Nina Goodman, Public Health
Advisor, Office of Communication and
Public Liaison, 9609 Medical Center
Drive, RM 2E446 Rockville, MD 20850
or call non-toll-free number (240) 276–
6600 or Email your request, including
your address to: nciocpl@mail.nih.gov.
Formal requests for additional plans and
instruments must be requested in
writing.
Proposed Collection: A Generic
Submission for Formative Research,
Pretesting and Customer Satisfaction of
NCI’s Communication and Education
Resources (NCI), 0925–0046, Expiration
SUMMARY:

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Federal Register / Vol. 81, No. 103 / Friday, May 27, 2016 / Notices

Date 05/31/2016, REVISION, National
Cancer Institute (NCI), National
Institutes of Health (NIH).
Need and Use of Information
Collection: As part of NCI’s mandate
from Congress to disseminate
information on cancer research,
detection, prevention, and treatment,
the Institute develops a wide variety of
messages and materials. Testing these
messages and materials assesses their
potential effectiveness in reaching and
communicating with their intended
audience while they are still in the
developmental stage and can be revised.
The formative research and pretesting

process thus contributes to maximizing
NCI’s limited dollar resources for
information dissemination and
education. NCI also must ensure the
relevance, utility, and appropriateness
of the many educational programs and
products that the Institute produces.
Customer satisfaction studies help NCI
identify modifications necessary to meet
the needs of NCI’s various target
audiences. Since the previous
submission, there have been 10
approved sub-studies with an approved
request of just under 1400 burden hours
over 2.5 years. Approval is requested for

the conduct of multiple studies
annually using such methods as
interviews, focus groups, and various
types of surveys. The content, timing,
and number of respondents to be
included in each sub-study will vary,
depending on the nature of the message/
material/program being assessed, the
methodology selected, and the target
audiences.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
33,000.

ESTIMATED ANNUALIZED BURDEN HOURS
Frequency of
response per
respondent

Time per
response
(in hours)

Form name

Healthcare Providers and Professionals including those working in
health field (e.g., cancer researchers).
General Public, Cancer Patients,
Friends and Families of Patients.

Focus Groups, Individual In-Depth
Interviews, Brief Interviews, Surveys, Website Usability Testing.

16,500

1

1

16,500

Focus Groups, Individual In-Depth
Interviews, Brief Interviews, Surveys, Website Usability Testing.

16,500

1

1

16,500

Totals .........................................

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

33,000

33,000

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

33,000

Dated: May 20, 2016.
Karla Bailey,
Project Clearance Liaison, National Cancer
Institute, NIH.

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) ways to enhance 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.

[FR Doc. 2016–12505 Filed 5–26–16; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration

Proposed Project: SAMHSA SOAR
Web-Based Data Form (OMB No. 0930–
0329)—REVISION

Agency Information Collection
Activities: Proposed Collection;
Comment Request

sradovich on DSK3TPTVN1PROD with NOTICES

Number of
respondents

Category of respondents

In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
proposed projects. To request more
information on the proposed projects or
to obtain a copy of the information
collection plans, call the SAMHSA
Reports Clearance Officer on (240) 276–
1243.
Comments are invited on: (a) Whether
the proposed collections of information
are necessary for the proper
performance of the functions of the

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In 2009 the Substance Abuse and
Mental Health Services Administration
(SAMHSA) of the U.S. Department of
Health and Human Services established
a Technical Assistance Center to assist
in the implementation of the SSI/SSDI
Outreach Access and Recovery (SOAR)
effort in all states. The primary objective
of SOAR is to improve the allowance
rate for Social Security Administration
(SSA) disability benefits for people who
are experiencing or at risk of
homelessness, and who have a serious
mental illness.
During the SOAR training, the
importance of keeping track of SSI/SSDI
applications through the process is
stressed. In response to requests from
states implementing SOAR, the

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Burden hours

Technical Assistance Center, under
SAMHSA’s direction, developed a webbased data form that case managers can
use to track the progress of submitted
applications, including decisions
received from SSA either on initial
application or on appeal. This
password-protected web-based data
form is hosted on the SOAR Web site
(https://soartrack.prainc.com). Use of
this form is completely voluntary.
In addition, data from the web-based
form can be compiled into reports on
decision results and the use of SOAR
core components, such as the SSA–1696
Appointment of Representative, which
allows SSA to communicate directly
with the case manager assisting with the
application. These reports will be
reviewed by agency directors, SOAR
state-level leads, and the national SOAR
Technical Assistance Center to quantify
the success of the effort overall and to
identify areas where additional
technical assistance is needed.
The changes to this form include
questions on military discharge status,
VA disability compensation, applicant
earnings per month, number of
consultative exams ordered, and
whether access to benefits facilitated
housing. Additionally, we added three
questions to the user registration form
that include county, funding source,
and SOAR training completed.

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