82 FR 12617 - Submission for OMB Review; 30-Day Comment Request; NCI Genomic Data Commons (GDC) Data Submission Request Form (National Cancer Institute)

DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health

Federal Register Volume 82, Issue 42 (March 6, 2017)

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. This proposed information collection was previously published in the Federal Register on Tuesday, November 8, 2016 page 78609 Vol. 81 No. 216 FR 78609 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.

[Federal Register Volume 82, Number 42 (Monday, March 6, 2017)]
[Notices]
[Pages 12617-12618]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2017-04255]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Submission for OMB Review; 30-Day Comment Request; NCI Genomic 
Data Commons (GDC) Data Submission Request Form (National Cancer 
Institute)

AGENCY: National Institutes of Health, HHS.

ACTION: Notice.

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SUMMARY: 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. This proposed information 
collection was previously published in the Federal Register on Tuesday, 
November 8, 2016 page 78609 Vol. 81 No. 216 FR 78609 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.

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: Louis M. Staudt, MD, Ph.D., Director, Center for 
Cancer Genomics, National Cancer Institute, Building 10, Room 5A02, 10 
Center Drive, Bethesda, MD 20814 or call non-toll-free number 301-402-
1892 or Email your request, including your address to: 
[email protected].

SUPPLEMENTARY INFORMATION: 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.
    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: NCI Genomic Data Commons (GDC) Data Submission 
Request Form, 0925-New, National Cancer Institute (NCI), National 
Institutes of Health (NIH).
    Need and Use of Information Collection: The purpose of the NCI 
Genomic Data Commons (GDC) Data Submission Request Form is to provide a 
vehicle for investigators to request submission of their cancer genomic 
data into the GDC in support of data sharing. The purpose is to also 
provide a mechanism for the GDC Data Submission Review Committee to 
review and assess the data submission request for applicability to the 
GDC mission. The scope of the form involves obtaining information from 
investigators that: (1) Would like to submit data about their study 
into the GDC, (2) are affiliated with studies that adhere to GDC data 
submission conditions. The benefits of the collection are that it 
provides the needed information for investigators to understand the 
types of studies and data that the GDC supports, and that it provides a 
standard mechanism for the GDC to assess incoming data submission 
requests.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 50 hours.

                                        Estimated Annualized Burden Hours
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                                                                     Number of     Average time
               Type of respondent                    Number of     responses per   per response    Total annual
                                                    respondents     respondent      (in hours)      burden hour
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Investigator (19-1040 Medical Scientists).......             200               1           15/60              50
                                                 ---------------------------------------------------------------
    Total.......................................             200             200  ..............              50
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[[Page 12618]]

    Dated: February 15, 2017.
Karla Bailey,
Project Clearance Liaison, National Cancer Institute, National 
Institutes of Health.
[FR Doc. 2017-04255 Filed 3-3-17; 8:45 am]
BILLING CODE 4140-01-P