Availability of the Draft Supplementary Risk Assessment for the Boston University (BU) National Emerging Infectious Diseases Laboratories (NEIDL); Public Hearing, 11140-11141 [2012-4266]
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11140
Federal Register / Vol. 77, No. 37 / Friday, February 24, 2012 / Notices
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Nancy Sheard, SCD,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6046–E,
MSC 7892, Bethesda, MD 20892, 301–408–
9901, sheardn@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Small
Business: Cell, Computational, and
Molecular Biology.
Date: March 15, 2012.
Time: 11 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: General Services Administration
Crystal City, Crystal City Plaza 4 (CP4), 2200
Crystal Drive, L–121, Arlington, VA 22202.
Contact Person: Maria DeBernardi, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6158,
MSC 7892, Bethesda, MD 20892, 301–435–
1355, debernardima@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Program
Project: Regulation of Mitochondrial
Oxidative Metabolism.
Date: March 20–21, 2012.
Time: 8 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Rolf Jakobi, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6187,
MSC 7806, Bethesda, MD 20892, 301–495–
1718, jakobir@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Muscle
Disease and Function.
Date: March 21–22, 2012.
Time:9 a.m. to 5 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Rajiv Kumar, Ph.D., Chief,
MOSS IRG, Center for Scientific Review,
National Institutes of Health, 6701 Rockledge
Drive, Room 4216, MSC 7802, Bethesda, MD
20892, 301–435–1212, kumarra@csr.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: February 16, 2012.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2012–4346 Filed 2–23–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Allergy and
Infectious Diseases; Notice of Closed
Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings 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
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
Allergy and Infectious Diseases Special
Emphasis Panel; Host Targeted Interventions
As Therapeutics For Infectious Diseases.
Date: March 13, 2012.
Time: 8 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6700B
Rockledge Drive, Bethesda, MD 20817
(Telephone Conference Call).
Contact Person: Raymond R. Schleef,
Ph.D., Scientific Review Officer, Scientific
Review Program, Division of Extramural
Activities, National Institutes of Health/
NIAID, 6700B Rockledge Drive, MSC 7616,
Bethesda, MD 20892–7616, 301–451–3679,
schleefrr@niaid.nih.gov.
Name of Committee: Microbiology,
Infectious Diseases and AIDS Initial Review
Group; Acquired Immunodeficiency
Syndrome Research Review Committee.
Date: March 14–15, 2012.
Time: 8:30 a.m. to 5:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: Residence Inn Bethesda, 7335
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Sujata Vijh, Ph.D.,
Scientific Review Officer, Scientific Review
Program, DEA/NIAID/NIH, 6700B Rockledge
Drive, MSC 7616, Bethesda, MD 20892–7616,
301–594–0985, vijhs@niaid.nih.gov.
Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel; Host Targeted Interventions
As Therapeutics For Infectious Diseases.
Date: March 15, 2012.
Time: 8 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6700B
Rockledge Drive, Bethesda, MD 20817
(Telephone Conference Call).
Contact Person: Raymond R. Schleef,
Ph.D., Scientific Review Officer, Scientific
Review Program, Division of Extramural
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Activities, National Institutes of Health/
NIAID, 6700B Rockledge Drive, MSC 7616,
Bethesda, MD 20892–7616, 301–451–3679,
schleefrr@niaid.nih.gov.
Name of Committee: National Institute of
Allergy and Infectious Diseases Special
Emphasis Panel; Host Targeted Interventions
As Therapeutics For Infectious Diseases.
Date: March 16, 2012.
Time: 8 a.m. to 6 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6700B
Rockledge Drive, Bethesda, MD 20817
(Telephone Conference Call).
Contact Person: Raymond R. Schleef,
Ph.D., Scientific Review Officer, Scientific
Review Program, Division of Extramural
Activities, National Institutes of Health/
NIAID, 6700B Rockledge Drive, MSC 7616,
Bethesda, MD 20892–7616, 301–451–3679,
schleefrr@niaid.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.855, Allergy, Immunology,
and Transplantation Research; 93.856,
Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
Dated: February 17, 2012.
Jennifer S. Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 2012–4343 Filed 2–23–12; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Availability of the Draft Supplementary
Risk Assessment for the Boston
University (BU) National Emerging
Infectious Diseases Laboratories
(NEIDL); Public Hearing
AGENCY:
National Institutes of Health,
HHS.
Notice; public hearing
announcement.
ACTION:
The National Institutes of
Health has placed in the docket for
public review and comment the Draft
Supplementary Risk Assessment for the
NEIDL, which is intended to respond to
the concerns of the local community,
courts, the National Research Council,
and the general public regarding
possible impacts of the laboratory. The
purpose of the Draft Supplementary
Risk Assessment for the NEIDL is to
present the human health consequences
of a potential accidental event or
malevolent action resulting in the
release of a pathogen or loss of
biological containment at the NEIDL.
Furthermore, this risk assessment
compares the potential public health
consequences resulting from the
potential loss of biocontainment in a
SUMMARY:
E:\FR\FM\24FEN1.SGM
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srobinson on DSK4SPTVN1PROD with NOTICES
Federal Register / Vol. 77, No. 37 / Friday, February 24, 2012 / Notices
range of population density areas that
represent urban, suburban, and rural
environments. The urban, suburban,
and rural sites that were selected for the
purposes of the comparative analysis
include the Boston University Medical
Campus (BUMC) BioSquare Research
Park, Boston, where the NEIDL has been
constructed; the BU Corporate
Education Center in Tyngsborough,
Massachusetts; and the BU Sargent
Center for Outdoor Education near
Peterborough, New Hampshire. The
Risk Assessment also examines whether
locating the NEIDL in Boston would
have a disproportionately high and
adverse impacts on low-income and
minority populations.
DATES: Comments on the Draft
Supplementary Risk Assessment for the
NEIDL must be postmarked no later
than May 1, 2012. A public hearing to
solicit public comment on the document
will be held on April 19, 2012, from
6:30–9:30 p.m. at Roxbury Community
College, 1234 Columbus Avenue,
Boston, MA 02120.
ADDRESSES: Written comments should
be sent to The National Institutes of
Health, Office of Biotechnology
Activities, ATTN: NEIDL Risk
Assessment, 6705 Rockledge Drive,
Suite 750, Bethesda, Maryland, 20892.
Email comments should be sent to
NIH_BRP@od.nih.gov. Please note that
comments sent by email must be
received by 11:59 p.m. on the last day
of the comment period May 1, 2012.
FOR FURTHER INFORMATION CONTACT:
National Institutes of Health Office of
Biotechnology Activities, 6705
Rockledge Drive, Suite 750, Bethesda,
Maryland, 20892. Telephone number:
301–496–9838. Electronic mail address:
NIH_BRP@od.nih.gov.
SUPPLEMENTARY INFORMATION: The
National Institutes of Health awarded a
construction grant to Boston University
Medical Campus to partly fund the
design and construction of one of two
National Biocontainment Laboratories.
These advanced biomedical research
laboratories are essential to the civilian
biodefense initiative, providing
critically needed Biosafety Levels 2, 3
and 4 research space. The basic and
translational research to be conducted
in these laboratories over the next 20
years would result in development of
new rapid diagnostic assays, vaccines
and therapeutics for protection of the
American public against intentional
misuse or release of harmful biological
agents or toxins and naturally emerging
and re-emerging infectious diseases.
The NIH completed and published a
final Environmental Impact Statement
(EIS) and published a Record of
VerDate Mar<15>2010
18:34 Feb 23, 2012
Jkt 226001
Decision as required for major federal
actions under the National
Environmental Policy Act. Construction
of the NEIDL began at the BioSquare II
Research Park on Albany Street, Boston,
Massachusetts adjacent to the BUMC.
During the preparation of the EIS, the
NIH conducted a thorough review of the
possible impacts of the NEIDL on the
public and the environment. Based on
that review, the NIH concluded that the
construction and operation of the NEIDL
in its current location posed a negligible
risk to the surrounding community in
which the laboratory was sited.
Several residents and public interest
groups filed a federal lawsuit
challenging the adequacy of the final
EIS prepared for the NEIDL and whether
the potential risks of the research would
vary depending on the location of the
facility in a suburban or rural area. A
state lawsuit was also filed challenging
the adequacy of a separate
environmental review prepared
pursuant to a Massachusetts law.
The Draft Supplementary Risk
Assessment for the NEIDL addresses the
issues raised by the public and the
courts regarding pathogen release,
facility location, and environmental
justice concerns.
Throughout the preparation of the
Draft Supplementary Risk Assessment
for the NEIDL, NIH has sought the input
of the public regarding scenarios and
pathogens they wished to see included
in the Risk Assessment. In addition,
NIH established an independent Blue
Ribbon Panel (BRP) to provide scientific
and technical advice to the agency in
assessing any potential public health
risks associated with the operation of
the NEIDL and to assess strategies for
mitigation. The BRP was convened with
16 members having expertise in relevant
fields, including infectious diseases,
public health and epidemiology, risk
assessment, environmental justice, risk
communications, bioethics, biodefense,
biosafety, and infectious disease
modeling. The NIH has also sought
guidance from the National Research
Council (NRC) committee that was
critical of the draft of an earlier risk
assessment prepared by the NIH.
Availability of Copies and Electronic
Access
Given the highly technical nature of
the report and in order to assist the
reader, a reader’s guide will be provided
with each copy of the draft
supplementary risk assessment .
Copies of the Draft Supplementary
Risk Assessment Report for the Boston
University National Emerging Infectious
Diseases Laboratory and the reader’s
guide document may be obtained at no
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11141
cost by calling 301–496–9838, or by
emailing requests to
NIH_BRP@od.nih.gov. The document
will also be available electronically at:
https://nihblueribbonpanel-bumcneidl.od.nih.gov/default.asp.
A copy of the draft supplementary
risk assessment and the reader’s guide
will also be available for review at each
of the following locations. Central
Branch of the Boston Public Library, 700
Boylston Street, Boston, MA, South End
Library, 685 Tremont Street, Boston,
MA, Grove Hall Library, 42 Geneva
Avenue, and Dudley Library, 65 Warren
Street, Boston, MA.
Public Meeting: The National
Institutes of Health will hold a public
meeting on Thursday, April 19, 2012,
from 6:30–9:30 p.m. at Roxbury
Community College, 1234 Columbus
Avenue, Boston, MA 02120. The
purpose of the meeting is to solicit
public comments regarding the Draft
Supplementary Risk Assessment for the
National Emerging Infectious Diseases
Laboratories. Comments provided
during the meeting, as well as those
received during the public comment
period will be considered in the Final
Supplementary Risk Assessment for the
National Emerging Infectious Diseases
Laboratories. Individuals wishing to
provide oral comments at the meeting
must sign-in prior to the start of the
meeting. Sign-in will begin at 5:30 p.m.
In order to ensure everyone has the
opportunity to speak, comments must
be limited to no longer than three
minutes. This public meeting is part of
the 67-day public comment period
initiated with the publication of a
Notice of Availability in the Federal
Register on February 24, 2012. The 67day comment period began on February
24, 2012 and will end on May 1, 2012.
Comments can also be sent to: The
National Institutes of Health, Attn:
NEIDL Risk Assessment, 6705
Rockledge Drive, Suite 750, Bethesda,
MD 20892, or emailed to
NIH_BRP@od.nih.gov. For further
information concerning this meeting,
please contact Office of Biotechnology
Activities, National Institutes of Health,
6705 Rockledge Drive, Suite 750,
Bethesda, MD 20892, telephone 301–
496–9838, email: BRP_NIH@od.nih.gov.
Dated: February 16, 2012.
Amy Patterson,
Associate Director for Science Policy,
National Institutes of Health.
[FR Doc. 2012–4266 Filed 2–23–12; 8:45 am]
BILLING CODE 4140–01–P
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Agencies
[Federal Register Volume 77, Number 37 (Friday, February 24, 2012)]
[Notices]
[Pages 11140-11141]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-4266]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Availability of the Draft Supplementary Risk Assessment for the
Boston University (BU) National Emerging Infectious Diseases
Laboratories (NEIDL); Public Hearing
AGENCY: National Institutes of Health, HHS.
ACTION: Notice; public hearing announcement.
-----------------------------------------------------------------------
SUMMARY: The National Institutes of Health has placed in the docket for
public review and comment the Draft Supplementary Risk Assessment for
the NEIDL, which is intended to respond to the concerns of the local
community, courts, the National Research Council, and the general
public regarding possible impacts of the laboratory. The purpose of the
Draft Supplementary Risk Assessment for the NEIDL is to present the
human health consequences of a potential accidental event or malevolent
action resulting in the release of a pathogen or loss of biological
containment at the NEIDL. Furthermore, this risk assessment compares
the potential public health consequences resulting from the potential
loss of biocontainment in a
[[Page 11141]]
range of population density areas that represent urban, suburban, and
rural environments. The urban, suburban, and rural sites that were
selected for the purposes of the comparative analysis include the
Boston University Medical Campus (BUMC) BioSquare Research Park,
Boston, where the NEIDL has been constructed; the BU Corporate
Education Center in Tyngsborough, Massachusetts; and the BU Sargent
Center for Outdoor Education near Peterborough, New Hampshire. The Risk
Assessment also examines whether locating the NEIDL in Boston would
have a disproportionately high and adverse impacts on low-income and
minority populations.
DATES: Comments on the Draft Supplementary Risk Assessment for the
NEIDL must be postmarked no later than May 1, 2012. A public hearing to
solicit public comment on the document will be held on April 19, 2012,
from 6:30-9:30 p.m. at Roxbury Community College, 1234 Columbus Avenue,
Boston, MA 02120.
ADDRESSES: Written comments should be sent to The National Institutes
of Health, Office of Biotechnology Activities, ATTN: NEIDL Risk
Assessment, 6705 Rockledge Drive, Suite 750, Bethesda, Maryland, 20892.
Email comments should be sent to NIH_BRP@od.nih.gov. Please note that
comments sent by email must be received by 11:59 p.m. on the last day
of the comment period May 1, 2012.
FOR FURTHER INFORMATION CONTACT: National Institutes of Health Office
of Biotechnology Activities, 6705 Rockledge Drive, Suite 750, Bethesda,
Maryland, 20892. Telephone number: 301-496-9838. Electronic mail
address: NIH_BRP@od.nih.gov.
SUPPLEMENTARY INFORMATION: The National Institutes of Health awarded a
construction grant to Boston University Medical Campus to partly fund
the design and construction of one of two National Biocontainment
Laboratories. These advanced biomedical research laboratories are
essential to the civilian biodefense initiative, providing critically
needed Biosafety Levels 2, 3 and 4 research space. The basic and
translational research to be conducted in these laboratories over the
next 20 years would result in development of new rapid diagnostic
assays, vaccines and therapeutics for protection of the American public
against intentional misuse or release of harmful biological agents or
toxins and naturally emerging and re-emerging infectious diseases.
The NIH completed and published a final Environmental Impact
Statement (EIS) and published a Record of Decision as required for
major federal actions under the National Environmental Policy Act.
Construction of the NEIDL began at the BioSquare II Research Park on
Albany Street, Boston, Massachusetts adjacent to the BUMC.
During the preparation of the EIS, the NIH conducted a thorough
review of the possible impacts of the NEIDL on the public and the
environment. Based on that review, the NIH concluded that the
construction and operation of the NEIDL in its current location posed a
negligible risk to the surrounding community in which the laboratory
was sited.
Several residents and public interest groups filed a federal
lawsuit challenging the adequacy of the final EIS prepared for the
NEIDL and whether the potential risks of the research would vary
depending on the location of the facility in a suburban or rural area.
A state lawsuit was also filed challenging the adequacy of a separate
environmental review prepared pursuant to a Massachusetts law.
The Draft Supplementary Risk Assessment for the NEIDL addresses the
issues raised by the public and the courts regarding pathogen release,
facility location, and environmental justice concerns.
Throughout the preparation of the Draft Supplementary Risk
Assessment for the NEIDL, NIH has sought the input of the public
regarding scenarios and pathogens they wished to see included in the
Risk Assessment. In addition, NIH established an independent Blue
Ribbon Panel (BRP) to provide scientific and technical advice to the
agency in assessing any potential public health risks associated with
the operation of the NEIDL and to assess strategies for mitigation. The
BRP was convened with 16 members having expertise in relevant fields,
including infectious diseases, public health and epidemiology, risk
assessment, environmental justice, risk communications, bioethics,
biodefense, biosafety, and infectious disease modeling. The NIH has
also sought guidance from the National Research Council (NRC) committee
that was critical of the draft of an earlier risk assessment prepared
by the NIH.
Availability of Copies and Electronic Access
Given the highly technical nature of the report and in order to
assist the reader, a reader's guide will be provided with each copy of
the draft supplementary risk assessment .
Copies of the Draft Supplementary Risk Assessment Report for the
Boston University National Emerging Infectious Diseases Laboratory and
the reader's guide document may be obtained at no cost by calling 301-
496-9838, or by emailing requests to NIH_BRP@od.nih.gov. The document
will also be available electronically at: https://nihblueribbonpanel-bumc-neidl.od.nih.gov/default.asp.
A copy of the draft supplementary risk assessment and the reader's
guide will also be available for review at each of the following
locations. Central Branch of the Boston Public Library, 700 Boylston
Street, Boston, MA, South End Library, 685 Tremont Street, Boston, MA,
Grove Hall Library, 42 Geneva Avenue, and Dudley Library, 65 Warren
Street, Boston, MA.
Public Meeting: The National Institutes of Health will hold a
public meeting on Thursday, April 19, 2012, from 6:30-9:30 p.m. at
Roxbury Community College, 1234 Columbus Avenue, Boston, MA 02120. The
purpose of the meeting is to solicit public comments regarding the
Draft Supplementary Risk Assessment for the National Emerging
Infectious Diseases Laboratories. Comments provided during the meeting,
as well as those received during the public comment period will be
considered in the Final Supplementary Risk Assessment for the National
Emerging Infectious Diseases Laboratories. Individuals wishing to
provide oral comments at the meeting must sign-in prior to the start of
the meeting. Sign-in will begin at 5:30 p.m. In order to ensure
everyone has the opportunity to speak, comments must be limited to no
longer than three minutes. This public meeting is part of the 67-day
public comment period initiated with the publication of a Notice of
Availability in the Federal Register on February 24, 2012. The 67-day
comment period began on February 24, 2012 and will end on May 1, 2012.
Comments can also be sent to: The National Institutes of Health, Attn:
NEIDL Risk Assessment, 6705 Rockledge Drive, Suite 750, Bethesda, MD
20892, or emailed to NIH_BRP@od.nih.gov. For further information
concerning this meeting, please contact Office of Biotechnology
Activities, National Institutes of Health, 6705 Rockledge Drive, Suite
750, Bethesda, MD 20892, telephone 301-496-9838, email: BRP_NIH@od.nih.gov.
Dated: February 16, 2012.
Amy Patterson,
Associate Director for Science Policy, National Institutes of Health.
[FR Doc. 2012-4266 Filed 2-23-12; 8:45 am]
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