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Federal Register / Vol. 85, No. 141 / Wednesday, July 22, 2020 / Notices
61. Kediala Magassouba, New York City,
New York, Court of Federal Claims
No: 20–0762V
62. James Sokol, Seattle, Washington,
Court of Federal Claims No: 20–
0763V
63. Joanie Arseneault, Melbourne,
Florida, Court of Federal Claims No:
20–0765V
64. Gregory Carter, Raleigh, North
Carolina, Court of Federal Claims
No: 20–0767V
65. Destiny Maynard and Elijah Bunch
on behalf of C. B., Deceased, East
Moline, Illinois, Court of Federal
Claims No: 20–0768V
66. Candice E. Hutchison, Belfast,
Maine, Court of Federal Claims No:
20–0773V
67. Kelly Steele, Baltimore, Maryland,
Court of Federal Claims No: 20–
0775V
68. Lorraine Ferrucci on behalf of J. B.,
Orchard Park, New York, Court of
Federal Claims No: 20–0776V
69. Lisa Black, St. Paul, Minnesota,
Court of Federal Claims No: 20–
0777V
70. Sharon Danberry, Mankato,
Minnesota, Court of Federal Claims
No: 20–0778V
71. Brianna Meyers, Albany, New York,
Court of Federal Claims No: 20–
0779V
72. Sandra Francis, Leesburg, Florida,
Court of Federal Claims No: 20–
0780V
73. Renee Byndloss, Chicago, Illinois,
Court of Federal Claims No: 20–
0781V
74. Juliet Wolf, Dresher, Pennsylvania,
Court of Federal Claims No: 20–
0782V
75. Larry Alex Klickstein, Pasadena,
California, Court of Federal Claims
No: 20–0785V
76. Antonios Tsamasiros, Rockaway
Beach, New York, Court of Federal
Claims No: 20–0786V
77. Patricia Parks, White Plains, New
York, Court of Federal Claims No:
20–0788V
78. Cheree Roach and Jason Roach on
behalf of I. R., Eagle River, Alaska,
Court of Federal Claims No: 20–
0789V
79. Jacqueline Stokes, Chicago, Illinois,
Court of Federal Claims No: 20–
0790V
80. Niberley Walton, Fort Belvoir,
Virginia, Court of Federal Claims
No: 20–0791V
81. Adam Smith, San Antonio, Texas,
Court of Federal Claims No: 20–
0794V
82. Nydia Ellentuch, Saint Cloud,
Florida, Court of Federal Claims No:
20–0795V
83. Julie Leibold, Blue Springs,
Missouri, Court of Federal Claims
No: 20–0796V
84. Keri H. Daigle, Richmond, Virginia,
Court of Federal Claims No: 20–
0797V
FOR FURTHER INFORMATION CONTACT:
Sherrette Funn, Sherrette.Funn@hhs.gov
or (202) 795–7714. When submitting
comments or requesting information,
please include the document identifier
0990–New–30D and project title for
reference.
Interested
persons are invited to send comments
regarding this burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
Title of the Collection: Resport of
Dental Examination of Applicants to the
Commissioned Corps of the U.S. Public
Health Service.
Type of Collection: Reinstatement.
OMB No.: 0990–0324.
Abstract: The Commissioned Corps of
the U.S. Public Health Service has a
need for the information in order to
assess the qualifications of each
applicant and make a determination
whether the applicant meets the
requirements to receive a commission.
The information is used to make
determinations on candidates/
applicants seeking appointment to the
Corps to assess their medical suitability.
The purpose is to evaluate the medical
suitability of applicants on the basis of
the Corps’ medical accession standards
and policy. The protected information is
accessed by appropriate personnel and
clinical reviewers. The form is not
disclosed to external entities, other than
for uses authorized by law.
Type of respondent; frequency
(annual); Applicants/Candidates to the
Commissioned Corps of the U.S. Public
Health Service.
SUPPLEMENTARY INFORMATION:
[FR Doc. 2020–15830 Filed 7–21–20; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–0324]
Agency Information Collection
Request: 30-Day Public Comment
Request
Office of the Secretary, Health
and Human Services (HHS).
ACTION: Notice.
AGENCY:
In compliance with the
requirement of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, is publishing the
following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be
received on or before August 21, 2020.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain . Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
SUMMARY:
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ESTIMATED ANNUALIZED BURDEN TABLE
Type of respondent
Number of
respondents
Number
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Annual ..............................................................................................................
1000
1
1
1000
Total ..........................................................................................................
1000
1
1
1000
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Federal Register / Vol. 85, No. 141 / Wednesday, July 22, 2020 / Notices
Sherrette A. Funn,
Office of the Secretary, Paperwork Reduction
Act Reports Clearance Officer.
[FR Doc. 2020–15786 Filed 7–21–20; 8:45 am]
BILLING CODE 4150–49–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Guidance on Elimination of
Institutional Review Board (IRB)
Review of Research Applications and
Proposals: 2018 Requirements
The Office for Human Research
Protections, Office of the Assistant
Secretary for Health, Office of the
Secretary, Department of Health and
Human Services (HHS).
ACTION: Notice
AGENCY:
The Office for Human
Research Protections (OHRP), Office of
the Assistant Secretary for Health, is
announcing the availability of a
guidance document titled, ‘‘Guidance
on Elimination of Institutional Review
Board (IRB) Review of Research
Applications and Proposals: 2018
Requirements.’’ The guidance document
provides OHRP’s first formal guidance
on this topic. The document, which is
available on OHRP’s website at https://
www.hhs.gov/ohrp/regulations-andpolicy/guidance/index.html, is intended
primarily for institutions, IRBs,
investigators, HHS funding agencies,
and others that may be responsible for
the review, conduct, or oversight of
nonexempt research involving human
subjects conducted or supported by
HHS. The guidance document
announced in this notice finalizes the
draft guidance that was made available
for public comment through a notice in
the Federal Register on July 25, 2018
(83 FR 35278). OHRP received 2
comments from individuals or
organizations on the draft document and
those comments were considered as the
guidance was finalized.
DATES: Comments on OHRP guidance
documents are welcome at any time.
ADDRESSES: Submit written requests for
a single copy of the guidance document
titled ‘‘Guidance on Elimination of
Institutional Review Board (IRB) Review
of Research Applications and Proposals:
2018 Requirements’’ to the Division of
Policy and Assurances, Office for
Human Research Protections, 1101
Wootton Parkway, Suite 200, Rockville,
MD 20852. Send one self-addressed
adhesive label to assist that office in
processing your request, or fax your
request to 240–453–8420. See the
SUPPLEMENTARY INFORMATION section for
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SUMMARY:
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information on electronic access to the
guidance document.
Submit written comments to:
Comments on Elimination of
Institutional Review Board (IRB) Review
of Research Applications and Proposals:
2018 Requirements Guidance, Office for
Human Research Protections, 1101
Wootton Parkway, Suite 200, Rockville,
MD 20852. Comments also may be sent
via email to ohrp@hhs.gov or via
facsimile at 240–453–8420.
FOR FURTHER INFORMATION CONTACT:
Irene Stith-Coleman, Ph.D., Office for
Human Research Protections, 1101
Wootton Parkway, Suite 200, Rockville,
MD 20852, 240–453–6700; email
Irene.Stith-Coleman@hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
OHRP is announcing the availability
of a guidance document titled
‘‘Guidance on Elimination of
Institutional Review Board (IRB) Review
of Research Applications and Proposals:
2018 Requirements.’’ The guidance
document provides OHRP’s first formal
guidance on this topic. The document is
intended primarily for institutions,
IRBs, investigators, HHS funding
agencies, and others that may be
responsible for the review, conduct, or
oversight of nonexempt research
involving human subjects conducted or
supported by HHS.
The guidance document applies to
nonexempt research involving human
subjects that is conducted or supported
by HHS. It provides guidance on the
elimination of the requirement in
section 45 CFR 46.103(f) of the pre-2018
Requirements that each application or
proposal for research undergo IRB
review and approval as part of the
certification process. This guidance also
addresses the requirement in the 2018
Requirements for certification of each
proposed research study prior to
initiation. In particular, the guidance
addresses the following two topics: (1)
Pre-2018 Requirements; and, (2) 2018
Requirements.
The guidance document announced
in this notice finalizes the draft
guidance that was made available for
public comment through a notice in the
Federal Register on July 25, 2018 (83 FR
35278).
II. Electronic Access
Persons with access may obtain the
draft guidance documents on OHRP’s
website at OHRP’s website at https://
www.hhs.gov/ohrp/regulations-andpolicy/guidance/index.html.
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Dated: July 16, 2020.
Jerry Menikoff,
Director, Office for Human Research
Protections.
[FR Doc. 2020–15808 Filed 7–21–20; 8:45 am]
BILLING CODE 4150–36–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications
and/or contract proposals and the
discussions could disclose confidential
trade secrets or commercial property
such as patentable material, and
personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Child Health and Human Development Initial
Review Group Biobehavioral and Behavioral
Sciences Subcommittee.
Date: October 23, 2020.
Time: 10:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: NIH/NICHD, 6710B Rockledge
Drive, Bethesda, MD 20892 (Virtual Meeting).
Contact Person: Clayton W. Mash, Ph.D.,
Scientific Review Branch, Eunice Kennedy
Shriver National Institute of Child Health
and Human Development, NIH 6710B,
Rockledge Drive, Rm. 2131A, Bethesda, MD
20892, (301) 496–6866, mashc@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.864, Population Research;
93.865, Research for Mothers and Children;
93.929, Center for Medical Rehabilitation
Research; 93.209, Contraception and
Infertility Loan Repayment Program, National
Institutes of Health, HHS)
Dated: July 16, 2020.
Ronald J. Livingston, Jr.,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2020–15783 Filed 7–21–20; 8:45 am]
BILLING CODE 4140–01–P
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File Type | application/pdf |
File Modified | 2020-07-22 |
File Created | 2020-07-22 |