81 FR 78609 - Proposed Collection; 60-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 81, Issue 216 (November 8, 2016)

In compliance with the requirement of the Paperwork Reduction Act of 1995 to provide opportunity for public comment on proposed data collection projects, the National Cancer Institute (NCI) will publish periodic summaries of propose projects to be submitted to the Office of Management and Budget (OMB) for review and approval.

[Federal Register Volume 81, Number 216 (Tuesday, November 8, 2016)]
[Notices]
[Pages 78609-78610]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2016-26891]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Proposed Collection; 60-Day Comment Request; NCI Genomic Data 
Commons (GDC) Data Submission Request Form (National Cancer Institute)

AGENCY: National Institutes of Health.

ACTION: Notice.

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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 National Cancer Institute (NCI) will publish 
periodic summaries of propose 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: 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]. 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 collected; and (4) Ways 
to minimizes 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: 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.

[[Page 78610]]



                                        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....................................             200               1           15/60              50
                                                 ---------------------------------------------------------------
    Total.......................................             200             200  ..............              50
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    Dated: November 1, 2016.
Karla Bailey,
Project Clearance Liaison, National Cancer Institute, National 
Institutes of Health.
[FR Doc. 2016-26891 Filed 11-7-16; 8:45 am]
BILLING CODE 4140-01-P