30-day notice

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Federal Register / Vol. 81, No. 38 / Friday, February 26, 2016 / Notices
evidence that environmental chemicals,
physical substances, or mixtures
(collectively referred to as ‘‘substances’’)
cause adverse health effects and
provides opinions on whether these
substances may be of concern given
what is known about current human
exposure levels. OHAT also organizes
workshops or state-of-the-science
evaluations to address issues of
importance in environmental health
sciences. Information about OHAT is
found at http://ntp.niehs.nih.gov/go/
ohat.
Background Information on NTP Peer
Review Panels: NTP panels are
technical, scientific advisory bodies
established on an ‘‘as needed’’ basis to
provide independent scientific peer
review and advise the NTP on agents of
public health concern, new/revised
toxicological test methods, or other
issues. These panels help ensure
transparent, unbiased, and scientifically
rigorous input to the program for its use
in making credible decisions about
human hazard, setting research and
testing priorities, and providing
information to regulatory agencies about
alternative methods for toxicity
screening. The NTP welcomes
nominations of scientific experts for
upcoming panels. Scientists interested
in serving on an NTP panel should
provide current curriculum vitae to the
FOR FURTHER INFORMATION CONTACT. The
authority for NTP panels is provided by
42 U.S.C. 217a; section 222 of the Public
Health Service (PHS) Act, as amended.
The panel is governed by the Federal
Advisory Committee Act, as amended (5
U.S.C. Appendix 2), which sets forth
standards for the formation and use of
advisory committees.
Dated: February 22, 2016.
John R. Bucher,
Associate Director, NTP.
[FR Doc. 2016–04102 Filed 2–25–16; 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: The National
Physician Survey of Precision
Medicine in Cancer Treatment (NCI)
Summary: 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 November 18, 2015 (80 FR
72077), 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: Janet S. de Moor, Ph.D., MPH,
Project Officer, Division of Cancer
Control and Population Sciences, 9609
Medical Center Drive, 3E438, MSC

9764, Rockville, MD, 20850 or call nontoll-free number 240–276–6806 or Email
your request, including your address to:
[email protected]. Formal requests
for additional plans and instruments
must be requested in writing.
Proposed Collection: The National
Physician Survey of Precision Medicine
in Cancer Treatment 0925–NEW,
National Cancer Institute (NCI),
National Institutes of Health (NIH).
Need and Use of Information
Collection: The purpose of this study is
to investigate the current practice of
precision medicine in cancer treatment
among medical oncologists in the U.S.
This is a nationally representative
survey designed to assess oncologists’
current and potential use of genomic
testing, to inform the development of
interventions to facilitate optimal use of
genomic testing and to improve patientphysician discussions of the risks,
possible benefits, and uncertainties
surrounding the use of these tests.
Current knowledge of this topic is
limited as there are no nationallyrepresentative studies on this topic to
date. There are only two non-federal
studies two that have examined
physicians’ knowledge and attitudes
regarding somatic genetic and genomic
testing. The survey will be administered
by mail and web to medical oncology
physicians across the U.S. Nonrespondents will be invited to complete
a follow-back survey to share their
reasons for not participating. The study
findings will inform NCI of relevant
issues and concerns relating to the
application of precision medicine to
current and future cancer treatment
patterns and practice. This information
will also inform the development of
new funding initiatives to optimize the
use of precision medicine in cancer
treatment. Additionally, information
collected as part of this survey will be
used to develop physician educational
materials to address barriers to precision
medicine in cancer care delivery.
OMB approval is requested for 2
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
350.

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TOTAL ANNUALIZED BURDEN HOURS
Form name

Type of
respondent

Telephone Screener .......................................
Precision Medicine Survey—Pilot Study ........
Precision Medicine Survey—Full Study ..........
Non-response Follow-back Survey .................

Receptionists ......................
Oncology Physicians ..........
Oncology Physicians ..........
Oncology Physicians ..........

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Number of
respondents

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Number of
responses per
respondent

775
175
600
40

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1
1
1
1

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Average
burden per
response
(in hours)
3/60
20/60
20/60
5/60

Total annual
burden hour
39
58
200
3

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Federal Register / Vol. 81, No. 38 / Friday, February 26, 2016 / Notices
TOTAL ANNUALIZED BURDEN HOURS—Continued

Telephone Reminder Script ............................

Receptionists ......................

600

1

5/60

50

Total .........................................................

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

1,375

2,190

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

350

FOR FURTHER INFORMATION CONTACT:

[FR Doc. 2016–04105 Filed 2–25–16; 8:45 am]
BILLING CODE 4140–01–P

DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
[1651–0008]

Agency Information Collection
Activities: Application for Identification
Card
U.S. Customs and Border
Protection, Department of Homeland
Security.
ACTION: 30-Day notice and request for
comments; Extension of an existing
collection of information.
AGENCY:

U.S. Customs and Border
Protection (CBP) of the Department of
Homeland Security will be submitting
the following information collection
request to the Office of Management and
Budget (OMB) for review and approval
in accordance with the Paperwork
Reduction Act: Application for
Identification Card (CBP Form 3078).
This is a proposed extension of an
information collection that was
previously approved. CBP is proposing
that this information collection be
extended with no change to the burden
hours or to the information collected.
This document is published to obtain
comments from the public and affected
agencies.
DATES: Written comments should be
received on or before March 28, 2016 to
be assured of consideration.
ADDRESSES: Interested persons are
invited to submit written comments on
this proposed information collection to
the Office of Information and Regulatory
Affairs, Office of Management and
Budget. Comments should be addressed
to the OMB Desk Officer for Customs
and Border Protection, Department of
Homeland Security, and sent via
electronic mail to oira_submission@
omb.eop.gov or faxed to (202) 395–5806.
SUMMARY:

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Average
burden per
response
(in hours)

Type of
respondent

Dated: February 11, 2016.
Karla Bailey,
Project Clearance Liaison, National Cancer
Institute, NIH.

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Number of
respondents

Number of
responses per
respondent

Form name

Requests for additional information
should be directed to Tracey Denning,
U.S. Customs and Border Protection,
Regulations and Rulings, Office of
International Trade, 90 K Street NE.,
10th Floor, Washington, DC 20229–
1177, at 202–325–0265.
SUPPLEMENTARY INFORMATION: This
proposed information collection was
previously published in the Federal
Register (80 FR 66915) on October 30,
2015, allowing for a 60-day comment
period. This notice allows for an
additional 30 days for public comments.
This process is conducted in accordance
with 5 CFR 1320.10. CBP invites the
general public and other Federal
agencies to comment on proposed and/
or continuing information collections
pursuant to the Paperwork Reduction
Act of 1995 (Pub. L. 104–13; 44 U.S.C.
3507). The comments should address:
(a) Whether the 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
estimates of the burden of the collection
of information; (c) ways to enhance the
quality, utility, and clarity of the
information to be collected; (d) ways to
minimize the burden, including the use
of automated collection techniques or
the use of other forms of information
technology; and (e) the annual costs to
respondents or record keepers from the
collection of information (total capital/
startup costs and operations and
maintenance costs). The comments that
are submitted will be summarized and
included in the CBP request for OMB
approval. All comments will become a
matter of public record. In this
document, CBP is soliciting comments
concerning the following information
collection:
Title: Application for Identification
Card.
OMB Number: 1651–0008.
Form Number: CBP Form 3078.
Abstract: CBP Form 3078, Application
for Identification Card, is filled out in
order to obtain an Identification Card
which is used to gain access to CBP
security areas. This form collects

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Total annual
burden hour

biographical information and is usually
completed by licensed Cartmen or
Lightermen whose duties require
receiving, transporting, or otherwise
handling imported merchandise which
has not been released from CBP custody.
This form is submitted to the local CBP
office at the port of entry that the
respondent will be requesting access to
the Federal Inspection Section. Form
3078 is authorized by 19 U.S.C. 66,
1551, 1555, 1565, 1624, 1641; and 19
CFR 112.42, 118, 122.182, and 146.6.
This form is accessible at: http://www.
cbp.gov/sites/default/files/documents/
CBP%20Form%203078.pdf.
Action: CBP proposes to extend the
expiration date of this information
collection with no change to the
estimated burden hours or to CBP Form
3078.
Type of Review: Extension (without
change).
Affected Public: Businesses.
Estimated Number of Respondents:
150,000.
Estimated Number of Total Annual
Responses: 150,000.
Estimated Time per Response: 17
minutes.
Estimated Total Annual Burden
Hours: 42,450.
Dated: February 22, 2016.
Tracey Denning,
Agency Clearance Officer, U.S. Customs and
Border Protection.
[FR Doc. 2016–04121 Filed 2–25–16; 8:45 am]
BILLING CODE 9111–14–P

DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
[1651–0014]

Agency Information Collection
Activities: Declaration for Free Entry of
Unaccompanied Articles
U.S. Customs and Border
Protection, Department of Homeland
Security.
ACTION: 60-Day notice and request for
comments; extension of an existing
collection of information.
AGENCY:

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