81 FR 9869 - Submission for OMB Review; 30-Day Comment Request: The National Physician Survey of Precision Medicine in Cancer Treatment (NCI)
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health Federal Register Volume 81, Issue 38 (February 26, 2016)
National Institutes of Health
Federal Register Volume 81, Issue 38 (February 26, 2016)
| Page Range | 9869-9870 | |
| FR Document | 2016-04105 |
[Federal Register Volume 81, Number 38 (Friday, February 26, 2016)] [Notices] [Pages 9869-9870] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-04105] ----------------------------------------------------------------------- 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, [email protected] 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 non-toll-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 patient-physician 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 nationally-representative 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. Non- respondents 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. Total Annualized Burden Hours ---------------------------------------------------------------------------------------------------------------- Average Type of Number of Number of burden per Total annual Form name respondent respondents responses per response (in burden hour respondent hours) ---------------------------------------------------------------------------------------------------------------- Telephone Screener............ Receptionists... 775 1 3/60 39 Precision Medicine Survey-- Oncology 175 1 20/60 58 Pilot Study. Physicians. Precision Medicine Survey-- Oncology 600 1 20/60 200 Full Study. Physicians. Non-response Follow-back Oncology 40 1 5/60 3 Survey. Physicians. [[Page 9870]] Telephone Reminder Script..... Receptionists... 600 1 5/60 50 --------------------------------------------------------------- Total..................... ................ 1,375 2,190 .............. 350 ---------------------------------------------------------------------------------------------------------------- Dated: February 11, 2016. Karla Bailey, Project Clearance Liaison, National Cancer Institute, NIH. [FR Doc. 2016-04105 Filed 2-25-16; 8:45 am] BILLING CODE 4140-01-P
![Federal Register / Vol. 81, No. 38 / Friday, February 26, 2016 / Notices 9869
evidence that environmental chemicals, DEPARTMENT OF HEALTH AND 9764, Rockville, MD, 20850 or call non-
physical substances, or mixtures HUMAN SERVICES toll-free number 240–276–6806 or Email
(collectively referred to as ‘‘substances’’) your request, including your address to:
cause adverse health effects and National Institutes of Health janet.demoor@nih.gov. Formal requests
provides opinions on whether these for additional plans and instruments
Submission for OMB Review; 30-Day must be requested in writing.
substances may be of concern given
Comment Request: The National Proposed Collection: The National
what is known about current human
Physician Survey of Precision Physician Survey of Precision Medicine
exposure levels. OHAT also organizes Medicine in Cancer Treatment (NCI)
workshops or state-of-the-science in Cancer Treatment 0925–NEW,
evaluations to address issues of Summary: Under the provisions of National Cancer Institute (NCI),
importance in environmental health Section 3507(a)(1)(D) of the Paperwork National Institutes of Health (NIH).
sciences. Information about OHAT is Reduction Act of 1995, the National Need and Use of Information
found at http://ntp.niehs.nih.gov/go/ Cancer Institute, the National Institutes Collection: The purpose of this study is
of Health, has submitted to the Office of to investigate the current practice of
ohat.
Management and Budget (OMB) a precision medicine in cancer treatment
Background Information on NTP Peer request for review and approval of the among medical oncologists in the U.S.
Review Panels: NTP panels are information collection listed below. This is a nationally representative
technical, scientific advisory bodies This proposed information collection survey designed to assess oncologists’
established on an ‘‘as needed’’ basis to was previously published in the Federal current and potential use of genomic
provide independent scientific peer Register on November 18, 2015 (80 FR testing, to inform the development of
review and advise the NTP on agents of 72077), and allowed 60-days for public interventions to facilitate optimal use of
public health concern, new/revised comment. No public comments were genomic testing and to improve patient-
toxicological test methods, or other received. The purpose of this notice is physician discussions of the risks,
issues. These panels help ensure to allow an additional 30 days for public possible benefits, and uncertainties
transparent, unbiased, and scientifically comment. The National Cancer Institute surrounding the use of these tests.
rigorous input to the program for its use (NCI), National Institutes of Health, may Current knowledge of this topic is
in making credible decisions about not conduct or sponsor, and the limited as there are no nationally-
human hazard, setting research and respondent is not required to respond representative studies on this topic to
testing priorities, and providing to, an information collection that has date. There are only two non-federal
information to regulatory agencies about been extended, revised, or implemented studies two that have examined
alternative methods for toxicity on or after October 1, 1995, unless it physicians’ knowledge and attitudes
displays a currently valid OMB control regarding somatic genetic and genomic
screening. The NTP welcomes
number. testing. The survey will be administered
nominations of scientific experts for
Direct Comments to OMB: Written by mail and web to medical oncology
upcoming panels. Scientists interested
comments and/or suggestions regarding physicians across the U.S. Non-
in serving on an NTP panel should respondents will be invited to complete
the item(s) contained in this notice,
provide current curriculum vitae to the a follow-back survey to share their
especially regarding the estimated
FOR FURTHER INFORMATION CONTACT. The reasons for not participating. The study
public burden and associated response
authority for NTP panels is provided by findings will inform NCI of relevant
time, should be directed to the: Office
42 U.S.C. 217a; section 222 of the Public of Management and Budget, Office of issues and concerns relating to the
Health Service (PHS) Act, as amended. Regulatory Affairs, OIRA_submission@ application of precision medicine to
The panel is governed by the Federal omb.eop.gov or by fax to 202–395–6974, current and future cancer treatment
Advisory Committee Act, as amended (5 Attention: NIH Desk Officer. patterns and practice. This information
U.S.C. Appendix 2), which sets forth Comment Due Date: Comments will also inform the development of
standards for the formation and use of regarding this information collection are new funding initiatives to optimize the
advisory committees. best assured of having their full effect if use of precision medicine in cancer
Dated: February 22, 2016. received within 30 days of the date of treatment. Additionally, information
this publication. collected as part of this survey will be
John R. Bucher,
For Further Information Contact: To used to develop physician educational
Associate Director, NTP. obtain a copy of the data collection materials to address barriers to precision
[FR Doc. 2016–04102 Filed 2–25–16; 8:45 am] plans and instruments, or request more medicine in cancer care delivery.
BILLING CODE 4140–01–P information on the proposed project, OMB approval is requested for 2
contact: Janet S. de Moor, Ph.D., MPH, years. There are no costs to respondents
Project Officer, Division of Cancer other than their time. The total
Control and Population Sciences, 9609 estimated annualized burden hours are
Medical Center Drive, 3E438, MSC 350.
TOTAL ANNUALIZED BURDEN HOURS
Average
Number of
Type of Number of burden per Total annual
Form name responses per
mstockstill on DSK4VPTVN1PROD with NOTICES
respondent respondents response burden hour
respondent (in hours)
Telephone Screener ....................................... Receptionists ...................... 775 1 3/60 39
Precision Medicine Survey—Pilot Study ........ Oncology Physicians .......... 175 1 20/60 58
Precision Medicine Survey—Full Study .......... Oncology Physicians .......... 600 1 20/60 200
Non-response Follow-back Survey ................. Oncology Physicians .......... 40 1 5/60 3
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![9870 Federal Register / Vol. 81, No. 38 / Friday, February 26, 2016 / Notices
TOTAL ANNUALIZED BURDEN HOURS—Continued
Average
Number of
Type of Number of burden per Total annual
Form name responses per
respondent respondents response burden hour
respondent (in hours)
Telephone Reminder Script ............................ Receptionists ...................... 600 1 5/60 50
Total ......................................................... ............................................. 1,375 2,190 ........................ 350
Dated: February 11, 2016. FOR FURTHER INFORMATION CONTACT: biographical information and is usually
Karla Bailey, Requests for additional information completed by licensed Cartmen or
Project Clearance Liaison, National Cancer should be directed to Tracey Denning, Lightermen whose duties require
Institute, NIH. U.S. Customs and Border Protection, receiving, transporting, or otherwise
[FR Doc. 2016–04105 Filed 2–25–16; 8:45 am] Regulations and Rulings, Office of handling imported merchandise which
BILLING CODE 4140–01–P International Trade, 90 K Street NE., has not been released from CBP custody.
10th Floor, Washington, DC 20229– This form is submitted to the local CBP
1177, at 202–325–0265. office at the port of entry that the
DEPARTMENT OF HOMELAND SUPPLEMENTARY INFORMATION: This respondent will be requesting access to
SECURITY proposed information collection was the Federal Inspection Section. Form
previously published in the Federal 3078 is authorized by 19 U.S.C. 66,
U.S. Customs and Border Protection Register (80 FR 66915) on October 30, 1551, 1555, 1565, 1624, 1641; and 19
2015, allowing for a 60-day comment CFR 112.42, 118, 122.182, and 146.6.
[1651–0008]
period. This notice allows for an This form is accessible at: http://www.
Agency Information Collection additional 30 days for public comments. cbp.gov/sites/default/files/documents/
Activities: Application for Identification This process is conducted in accordance CBP%20Form%203078.pdf.
Card with 5 CFR 1320.10. CBP invites the Action: CBP proposes to extend the
general public and other Federal expiration date of this information
AGENCY: U.S. Customs and Border agencies to comment on proposed and/ collection with no change to the
Protection, Department of Homeland or continuing information collections estimated burden hours or to CBP Form
Security. pursuant to the Paperwork Reduction 3078.
ACTION: 30-Day notice and request for Act of 1995 (Pub. L. 104–13; 44 U.S.C. Type of Review: Extension (without
comments; Extension of an existing 3507). The comments should address: change).
collection of information. (a) Whether the collection of Affected Public: Businesses.
information is necessary for the proper Estimated Number of Respondents:
SUMMARY: U.S. Customs and Border performance of the functions of the 150,000.
Protection (CBP) of the Department of agency, including whether the Estimated Number of Total Annual
Homeland Security will be submitting information shall have practical utility; Responses: 150,000.
the following information collection (b) the accuracy of the agency’s Estimated Time per Response: 17
request to the Office of Management and estimates of the burden of the collection minutes.
Budget (OMB) for review and approval of information; (c) ways to enhance the Estimated Total Annual Burden
in accordance with the Paperwork quality, utility, and clarity of the Hours: 42,450.
Reduction Act: Application for information to be collected; (d) ways to Dated: February 22, 2016.
Identification Card (CBP Form 3078). minimize the burden, including the use
This is a proposed extension of an Tracey Denning,
of automated collection techniques or Agency Clearance Officer, U.S. Customs and
information collection that was the use of other forms of information
previously approved. CBP is proposing Border Protection.
technology; and (e) the annual costs to [FR Doc. 2016–04121 Filed 2–25–16; 8:45 am]
that this information collection be respondents or record keepers from the
extended with no change to the burden collection of information (total capital/
BILLING CODE 9111–14–P
hours or to the information collected. startup costs and operations and
This document is published to obtain maintenance costs). The comments that
comments from the public and affected DEPARTMENT OF HOMELAND
are submitted will be summarized and SECURITY
agencies. included in the CBP request for OMB
DATES: Written comments should be approval. All comments will become a U.S. Customs and Border Protection
received on or before March 28, 2016 to matter of public record. In this
be assured of consideration. document, CBP is soliciting comments [1651–0014]
ADDRESSES: Interested persons are concerning the following information
invited to submit written comments on collection: Agency Information Collection
this proposed information collection to Title: Application for Identification Activities: Declaration for Free Entry of
Unaccompanied Articles
mstockstill on DSK4VPTVN1PROD with NOTICES
the Office of Information and Regulatory Card.
Affairs, Office of Management and OMB Number: 1651–0008. AGENCY: U.S. Customs and Border
Budget. Comments should be addressed Form Number: CBP Form 3078. Protection, Department of Homeland
to the OMB Desk Officer for Customs Abstract: CBP Form 3078, Application Security.
and Border Protection, Department of for Identification Card, is filled out in
ACTION: 60-Day notice and request for
Homeland Security, and sent via order to obtain an Identification Card
comments; extension of an existing
electronic mail to oira_submission@ which is used to gain access to CBP
collection of information.
omb.eop.gov or faxed to (202) 395–5806. security areas. This form collects
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Document Created: 2018-02-02 14:37:16
Document Modified: 2018-02-02 14:37:16
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| 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. | |
| 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 non-toll-free number 240-276-6806 or Email your request, including your | |
| FR Citation | 81 FR 9869 |
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