Submission for OMB Review; 30-Day Comment Request: The Genetic Testing Registry, 15013 [2015-06370]
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Federal Register / Vol. 80, No. 54 / Friday, March 20, 2015 / Notices
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Dated: March 17, 2015.
Jeffrey A. Koses,
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Acquisition Policy, Office of Governmentwide Policy.
[FR Doc. 2015–06422 Filed 3–19–15; 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: The Genetic
Testing Registry
Under the provisions of
section 3507(a)(1)(D) of the Paperwork
SUMMARY:
Office of Clinical Research and
Bioethics Policy, Office of Science
Policy, NIH, 6705 Rockledge Dr., Suite
750, Bethesda, MD 20892, or call nontoll-free number (301) 496–9838, or
Email your request, including your
address to: OCRBP-OSP@od.nih.gov.
Formal requests for additional plans and
instruments must be requested in
writing.
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 November 25,
2014 (79 FR 70194), and allowed 60days for public comment. No public
comments were received. The purpose
of this notice is to allow an additional
30 days for public comment. The Office
of the Director (OD), 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.
DATES: 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: Ms. Sarah Carr, Acting Director,
Proposed Collection: The Genetic
Testing Registry, 0925–0651,
Reinstatment Without Change,—Office
of the Director (OD), National Institutes
of Health (NIH)
Need and Use of Information
Collection: Clinical laboratory tests are
available for more than 5,000 genetic
conditions. The Genetic Testing Registry
(GTR) provides a centralized, online
location for test developers,
manufacturers, and researchers to
voluntarily submit detailed information
about the availability and scientific
basis of their genetic tests. The GTR is
of value to clinicians by providing
information about the accuracy,
validity, and usefulness of genetic tests.
The GTR also highlights evidence gaps
where additional research is needed.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
5,536.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total annual
burden hours
Type of respondent
Form name
Laboratory Personnel Using Bulk
Submission.
Minimal Fields ..................................
190
29
18/60
1,653
Optional Fields .................................
Minimal Fields ..................................
159
116
29
29
14/60
30/60
1,076
1,682
Optional Fields .................................
97
29
24/60
1,125
Laboratory Personnel
Bulk Submission.
Not
Using
Dated: March 13, 2015.
Lawrence A. Tabak,
Deputy Director, National Institutes of Health.
mstockstill on DSK4VPTVN1PROD with NOTICES
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]]>Agencies
[Federal Register Volume 80, Number 54 (Friday, March 20, 2015)]
[Notices]
[Page 15013]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-06370]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day Comment Request: The Genetic
Testing Registry
SUMMARY: Under the provisions of 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. This
proposed information collection was previously published in the Federal
Register on November 25, 2014 (79 FR 70194), 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 Office
of the Director (OD), 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.
DATES: 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: Ms. Sarah Carr, Acting Director, Office of
Clinical Research and Bioethics Policy, Office of Science Policy, NIH,
6705 Rockledge Dr., Suite 750, Bethesda, MD 20892, or call non-toll-
free number (301) 496-9838, or Email your request, including your
address to: OCRBP-OSP@od.nih.gov. Formal requests for additional plans
and instruments must be requested in writing.
Proposed Collection: The Genetic Testing Registry, 0925-0651,
Reinstatment Without Change,--Office of the Director (OD), National
Institutes of Health (NIH)
Need and Use of Information Collection: Clinical laboratory tests
are available for more than 5,000 genetic conditions. The Genetic
Testing Registry (GTR) provides a centralized, online location for test
developers, manufacturers, and researchers to voluntarily submit
detailed information about the availability and scientific basis of
their genetic tests. The GTR is of value to clinicians by providing
information about the accuracy, validity, and usefulness of genetic
tests. The GTR also highlights evidence gaps where additional research
is needed.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 5,536.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondent Form name Number of responses per per response Total annual
respondents respondent (in hours) burden hours
----------------------------------------------------------------------------------------------------------------
Laboratory Personnel Using Minimal Fields.. 190 29 18/60 1,653
Bulk Submission.
Optional Fields. 159 29 14/60 1,076
Laboratory Personnel Not Using Minimal Fields.. 116 29 30/60 1,682
Bulk Submission.
Optional Fields. 97 29 24/60 1,125
----------------------------------------------------------------------------------------------------------------
Dated: March 13, 2015.
Lawrence A. Tabak,
Deputy Director, National Institutes of Health.
[FR Doc. 2015-06370 Filed 3-19-15; 8:45 am]
BILLING CODE 4140-01-P
