Draft Report on Carcinogens Monographs for 1-Bromopropane and Cumene; Availability of Documents; Request for Comments; Notice of Meeting, 4419-4421 [2013-01242]
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Dated: January 15, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
tkelley on DSK3SPTVN1PROD with
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: Center for Scientific
Review Special Emphasis Panel, Member
Conflict: Cardiovascular Sciences.
Date: February 7–8, 2013.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Bradley Nuss, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4142,
MSC7814, Bethesda, MD 20892, 301–451–
8754, nussb@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, PAR–10–
244, Structure and Function of Opioid
Receptors.
Date: February 11–12, 2013.
Time: 8:00 a.m. to 12:00 p.m.
VerDate Mar<15>2010
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Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: David R. Jollie, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4150,
MSC 7806, Bethesda, MD 20892, (301) 435–
1722, jollieda@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Biomedical
Imaging and Engineering Area Review.
Date: February 12, 2013.
Time: 1:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Jan Li, MD, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5106,
Bethesda, MD 20892, 301–435–1049, lij21@
csr.nih.gov.
Name of Committee: Vascular and
Hematology Integrated Review Group,
Hypertension and Microcirculation Study
Section.
Date: February 14, 2013.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Dallas Marriott Suites Medical—
Market Center, 2493 North Stemmons
Freeway, Dallas, TX 75207.
Contact Person: Ai-Ping Zou, MD, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4118,
MSC 7814, Bethesda, MD 20892, 301–408–
9497, zouai@csr.nih.gov.
Name of Committee: Infectious Diseases
and Microbiology Integrated Review Group,
Bacterial Pathogenesis Study Section.
Date: February 19, 2013.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Residence Inn Bethesda, 7335
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Richard G Kostriken,
Ph.D., Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3192,
MSC 7808, Bethesda, MD 20892, 301–402–
4454, kostrikr@csr.nih.gov.
Name of Committee: Vascular and
Hematology Integrated Review Group,
Molecular and Cellular Hematology Study
Section.
Date: February 19–20, 2013.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Embassy Suites at the Chevy Chase
Pavilion, 4300 Military Road NW.,
Washington, DC 20015.
Contact Person: Luis Espinoza, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 6183,
MSC 7804, Bethesda, MD 20892, 301–495–
1213, espinozala@mail.nih.gov.
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Name of Committee: Center for Scientific
Review Special Emphasis Panel, Member
Conflict: Integrative Neuroscience.
Date: February 19, 2013.
Time: 9:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Nicholas Gaiano, Scientific
Review Officer, Center for Scientific Review,
National Institutes of Health, 6701 Rockledge
Drive, Room 5178, MSC 7844, Bethesda, MD
20892–7844, 301–435–1033,
gaianonr@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Member
Conflict: Nanotechnology and Molecular
Substrates in Brain and Retinal Disorders.
Date: February 19, 2013.
Time: 12:00 p.m. to 3:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Yvonne Bennett, Scientific
Review Officer, Center for Scientific Review,
National Institutes of Health, 6701 Rockledge
Drive, Room 5199, MSC 7846, Bethesda, MD
20892, 301–379–3793, bennetty@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: January 15, 2013.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2013–01096 Filed 1–18–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
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National Institutes of Health
Draft Report on Carcinogens
Monographs for 1-Bromopropane and
Cumene; Availability of Documents;
Request for Comments; Notice of
Meeting
Peer review meeting of the
Draft Report on Carcinogens (RoC)
Monographs for 1-Bromopropane and
Cumene. These documents were
prepared by the Office of the Report on
Carcinogens (ORoC), Division of the
National Toxicology Program (DNTP),
National Institute of Environmental
Health Sciences (NIEHS).
DATES: Meeting: March 21, 2013, 1:00
p.m. to approximately 5:00 p.m. Eastern
Daylight Time (EDT) and March 22,
2013, from 8:30 a.m. until adjournment,
approximately 2:00 p.m. EDT.
Document Availability: Draft
monographs will be available by January
SUMMARY:
E:\FR\FM\22JAN1.SGM
22JAN1
4420
Federal Register / Vol. 78, No. 14 / Tuesday, January 22, 2013 / Notices
23, 2013, at https://ntp.niehs.nih.gov/go/
36639.
Public Comments Submissions:
Deadline is March 7, 2013.
Pre-Registration for Meeting and/or
Oral Comments: Deadline is March 19,
2013.
ADDRESSES: Meeting Location: NIEHS,
Keystone Building, Room 1003AB, 530
Davis Drive, Morrisville, NC 27560.
Agency Meeting Web page: The draft
monographs, draft agenda, registration
and other meeting materials are at
https://ntp.niehs.nih.gov/go/36639.
Webcast: The meeting will be
available via webcast at https://
www.niehs.nih.gov/news/video/
index.cfm.
Dr.
Lori D. White, NTP Designated Federal
Official, Office of Liaison, Policy and
Review, DNTP, NIEHS, P.O. Box 12233,
MD K2–03, Research Triangle Park, NC
27709. Phone: (919) 541–9834, Fax:
(301) 480–3272, Email:
whiteld@niehs.nih.gov. Hand Delivery/
Courier: 530 Davis Drive, Room 2136,
Morrisville, NC 27560.
SUPPLEMENTARY INFORMATION:
Background: The Report on Carcinogens
(RoC) is a congressionally mandated,
science-based, public health report that
identifies agents, substances, mixtures,
or exposures (collectively called
‘‘substances’’) in our environment that
may put people in the United States at
increased risk for cancer. The NTP
prepares the RoC on behalf of the
Secretary of Health and Human
Services.
The NTP follows an established, fourpart process for preparation of the RoC
(https://ntp.niehs.nih.gov/go/rocprocess).
A RoC Monograph is prepared for each
candidate substance selected for review
for the RoC. 1-Bromopropane and
cumene were selected as candidate
substances following solicitation of
public comment and review by the NTP
Board of Scientific Counselors review
on June 21–22, 2012 (https://
ntp.niehs.nih.gov/go/9741). A draft RoC
monograph consists of a (1) cancer
evaluation component that reviews all
information that may bear on a listing
decision, assesses its quality and
sufficiency for reaching a listing
decision, applies the RoC listing criteria
to the relevant scientific information,
and recommends a listing status for the
candidate substance in the RoC and (2)
a substance profile that contains the
NTP’s preliminary listing
recommendation and a summary of the
scientific evidence considered key to
reaching that recommendation. This
meeting is planned for peer review of
tkelley on DSK3SPTVN1PROD with
FOR FURTHER INFORMATION CONTACT:
VerDate Mar<15>2010
18:11 Jan 18, 2013
Jkt 229001
the draft RoC Monographs for 1bromopropane and cumene.
1-Bromopropane (CASRN 106–94–5)
is a brominated hydrocarbon that is
currently used as a solvent in a variety
of industrial and commercial
applications. It is used as a solvent
cleaner to degrease electronics,
precision optics, and metals, as a
solvent vehicle in industries that use
aerosolized adhesives (e.g., foam
cushion manufacturing), as a spot
remover in the textile industry, and as
a solvent in the dry cleaning industry.
Additional information about the review
of 1-bromopropane for the RoC is
available at https://ntp.niehs.nih.gov/go/
37896.
Cumene (CASRN 98–82–8,
isopropylbenzene) is an alkylated
benzene found in fossil fuels, such as
blended gasoline and kerosene, and
products of incomplete combustion. It is
a high production volume chemical in
the United States with the majority of its
use in the synthesis of acetone and
phenol. Additional information about
the review of cumene for the RoC is
available at https://ntp.niehs.nih.gov/go/
37895.
Meeting and Registration: The
meeting is open to the public with time
set aside for oral public comment;
attendance at the NIEHS is limited only
by the space available. The meeting is
scheduled for March 21, 2013, 1:00 p.m.
to approximately 5:00 p.m. EDT and
March 22, 2013, from 8:30 a.m. until
adjournment, approximately 2:00 p.m.
EDT. Two days are set aside for the
meeting; however, it may adjourn
sooner if the panel completes its peer
review of the draft monographs. Preregistration to attend the meeting and/
or provide oral comments is by March
19, 2013, at https://ntp.niehs.nih.gov/go/
36639. Visitor and security information
is available at https://www.niehs.nih.gov/
about/visiting/index.cfm. Individuals
with disabilities who need
accommodation to participate in this
event should contact Danica Andrews at
phone: (919) 541–2595 or email:
andrewsda@niehs.nih.gov. TTY users
should contact the Federal TTY Relay
Service at (800) 877–8339. Requests
should be made at least five business
days in advance of the event.
The preliminary agenda and draft
monographs should be posted on the
NTP Web site (https://ntp.niehs.nih.gov/
go/36639) by January 23, 2013.
Additional information will be posted
when available or may be requested in
hardcopy, see FOR FURTHER INFORMATION
CONTACT. Following the meeting, a
report of the peer review will be
prepared and made available on the
NTP Web site. Registered attendees are
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encouraged to access the meeting Web
page to stay abreast of the most current
information regarding the meeting.
Request for Comments: The NTP
invites written and oral public
comments on the draft monographs. The
deadline for submission of written
comments is March 7, 2013, to enable
review by the peer review panel and
NTP staff prior to the meeting. Preregistration to provide oral comments is
by March 19, 2013, at https://
ntp.niehs.nih.gov/go/36639. Public
comments and any other
correspondence on the draft
monographs should be sent to the FOR
FURTHER INFORMATION CONTACT. Persons
submitting written comments should
include their name, affiliation, mailing
address, phone, email, and sponsoring
organization (if any) with the document.
Written comments received in response
to this notice will be posted on the NTP
Web site, and the submitter will be
identified by name, affiliation, and/or
sponsoring organization.
Public comment at this meeting is
welcome, with time set aside for the
presentation of oral comments on the
draft monographs. In addition to inperson oral comments at the meeting at
the NIEHS, public comments can be
presented by teleconference line. There
will be 50 lines for this call; availability
will be on a first-come, first-served
basis. The lines will be open from 1:00
p.m. until approximately 5:00 p.m. EDT
on March 21 and from 8:30 a.m. EDT
until adjournment on March 22,
although oral comments will be
received only during the formal public
comment periods indicated on the
preliminary agenda. Each organization
is allowed one time slot. At least 7
minutes will be allotted to each speaker,
and if time permits, may be extended to
10 minutes at the discretion of the chair.
Persons wishing to make an oral
presentation are asked to register online
at https://ntp.niehs.nih.gov/go/36639 by
March 19, 2013, and if possible, to send
a copy of their slides and/or statement
or talking points at that time. Written
statements can supplement and may
expand the oral presentation.
Registration for oral comments will also
be available at the meeting, although
time allowed for presentation by on-site
registrants may be less than that for preregistered speakers and will be
determined by the number of speakers
who register on-site.
Background Information on the RoC:
Published biennially, each edition of the
RoC is cumulative and consists of
substances newly reviewed in addition
to those listed in previous editions. The
12th RoC, the latest edition, was
published on June 10, 2011 (available at
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22JAN1
Federal Register / Vol. 78, No. 14 / Tuesday, January 22, 2013 / Notices
https://ntp.niehs.nih.gov/go/roc12). The
13th RoC is under development. For
each listed substance, the RoC contains
a substance profile, which provides
information on: Cancer studies that
support the listing—including those in
humans, animals, and studies on
possible mechanisms of action—
information about potential sources of
exposure to humans, and current
Federal regulations to limit exposures.
Background Information on NTP Peer
Review Panels: NTP panels are
technical, scientific advisory bodies
established on an ‘‘as needed’’ basis to
provide independent scientific peer
review and advise the NTP on agents of
public health concern, new/revised
toxicological test methods, or other
issues. These panels help ensure
transparent, unbiased, and scientifically
rigorous input to the program for its use
in making credible decisions about
human hazard, setting research and
testing priorities, and providing
information to regulatory agencies about
alternative methods for toxicity
screening. The NTP welcomes
nominations of scientific experts for
upcoming panels. Scientists interested
in serving on an NTP panel should
provide a current curriculum vitae to
the FOR FURTHER INFORMATION CONTACT.
The authority for NTP panels is
provided by 42 U.S.C. 217a; section 222
of the Public Health Service (PHS) Act,
as amended. The panel is governed by
the Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), which
sets forth standards for the formation
and use of advisory committees.
Dated: January 16, 2013.
John R. Bucher,
Associate Director, National Toxicology
Program.
[FR Doc. 2013–01242 Filed 1–18–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
tkelley on DSK3SPTVN1PROD with
National Institute on Drug Abuse;
Notice of Closed Meetings
[FR Doc. 2013–01100 Filed 1–18–13; 8:45 am]
BILLING CODE 4140–01–P
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 contract proposals and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable materials,
18:11 Jan 18, 2013
Jkt 229001
Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel;
Development of Predictive In vivo Screening
Systems for Phenotypic Drug Discovery
(7786).
Date: January 25, 2013.
Time: 1:00 p.m. to 3:30 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Telephone
Conference Call).
Contact Person: Gerald L. McLaughlin,
Ph.D., Scientific Review Officer, Office of
Extramural Affairs, National Institute on
Drug Abuse, NIH, DHHS, 6001 Executive
Blvd., Room 4238, MSC 9550, Bethesda, MD
20892–9550, 301–402–6626,
gm145a@nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
Name of Committee: National Institute on
Drug Abuse Special Emphasis Panel; SBIR
Topic 148 Review Meeting (4418)
Date: January 30, 2013.
Time: 8:30 a.m. to 3:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852,
Contact Person: Jose F. Ruiz, Ph.D.,
Scientific Review Officer, Office of
Extramural Affairs, National Institute on
Drug Abuse, NIH, Room 4228, MSC 9550,
6001 Executive Blvd., Bethesda, MD 20892–
9550, (301) 451–3086, ruizjf@nida.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
(Catalogue of Federal Domestic Assistance
Program Nos.: 93.279, Drug Abuse and
Addiction Research Programs, National
Institutes of Health, HHS)
Dated: January 15, 2013.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
National Institutes of Health
VerDate Mar<15>2010
and personal information concerning
individuals associated with the contract
proposals, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Center for Advancing
Translational Sciences; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
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Sfmt 4703
4421
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 contract and grant
proposals and the discussions could
disclose confidential trade secrets or
commercial property such as patentable
material, and personal information
concerning individuals associated with
the contract proposals, the disclosure of
which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: National Center for
Advancing Translational Sciences Special
Emphasis Panel; Therapeutics Discovery.
Date: February 13–14, 2013.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health/
NCATS/OR, Democracy 1, Room 1080, 6701
Democracy Blvd., Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Barbara J. Nelson, Ph.D.,
Scientific Review Officer, Office of Grants
Management & Scientific Review, National
Center for Advancing Translational Sciences
(NCATS), National Institutes of Health, 6701
Democracy Blvd., Room 1080, 1 Dem. Plaza,
Bethesda, MD 20892–4874, 301–435–0806,
nelsonbj@mail.nih.gov.
Name of Committee: National Center for
Advancing Translational Sciences Special
Emphasis Panel; TRND–1.
Date: February 28–March 1, 2013.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate contract
proposals.
Place: Bethesda North Marriott Hotel &
Conference Center, Montgomery County
Conference Center Facility, 5701 Marinelli
Road, North Bethesda, MD 20852.
Contact Person: Guo He Zhang, Ph.D.,
MPH, Scientific Review Officer, Office of
Grants Management & Scientific Review,
National Center for Advancing Translational
Sciences (NCATS), National Institutes of
Health, 6701 Democracy Blvd., Democracy 1,
Room 1064, Bethesda, MD 20892–4874, 301–
435–0812, zhanggu@mail.nih.gov.
Name of Committee: National Center for
Advancing Translational Sciences Special
Emphasis Panel; TRND–3.
Date: March 13–14, 2013.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Gaithersburg Marriott
Washingtonian Center, 9751 Washingtonian
Boulevard, Gaithersburg, MD 20878.
Contact Person: Sheri A. Hild, Scientific
Review Officer, Office of Grants Management
& Scientific Review, National Center for
Advancing Translational Sciences (NCATS),
National Institutes of Health, 6701
Democracy Blvd., Democracy 1, Room 1082,
Bethesda, MD 20892–4874, 301–435–0811,
hildsa@mail.nih.gov.
E:\FR\FM\22JAN1.SGM
22JAN1
Agencies
[Federal Register Volume 78, Number 14 (Tuesday, January 22, 2013)]
[Notices]
[Pages 4419-4421]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-01242]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Draft Report on Carcinogens Monographs for 1-Bromopropane and
Cumene; Availability of Documents; Request for Comments; Notice of
Meeting
SUMMARY: Peer review meeting of the Draft Report on Carcinogens (RoC)
Monographs for 1-Bromopropane and Cumene. These documents were prepared
by the Office of the Report on Carcinogens (ORoC), Division of the
National Toxicology Program (DNTP), National Institute of Environmental
Health Sciences (NIEHS).
DATES: Meeting: March 21, 2013, 1:00 p.m. to approximately 5:00 p.m.
Eastern Daylight Time (EDT) and March 22, 2013, from 8:30 a.m. until
adjournment, approximately 2:00 p.m. EDT.
Document Availability: Draft monographs will be available by
January
[[Page 4420]]
23, 2013, at https://ntp.niehs.nih.gov/go/36639.
Public Comments Submissions: Deadline is March 7, 2013.
Pre-Registration for Meeting and/or Oral Comments: Deadline is
March 19, 2013.
ADDRESSES: Meeting Location: NIEHS, Keystone Building, Room 1003AB, 530
Davis Drive, Morrisville, NC 27560.
Agency Meeting Web page: The draft monographs, draft agenda,
registration and other meeting materials are at https://ntp.niehs.nih.gov/go/36639.
Webcast: The meeting will be available via webcast at https://www.niehs.nih.gov/news/video/index.cfm.
FOR FURTHER INFORMATION CONTACT: Dr. Lori D. White, NTP Designated
Federal Official, Office of Liaison, Policy and Review, DNTP, NIEHS,
P.O. Box 12233, MD K2-03, Research Triangle Park, NC 27709. Phone:
(919) 541-9834, Fax: (301) 480-3272, Email: whiteld@niehs.nih.gov. Hand
Delivery/Courier: 530 Davis Drive, Room 2136, Morrisville, NC 27560.
SUPPLEMENTARY INFORMATION: Background: The Report on Carcinogens (RoC)
is a congressionally mandated, science-based, public health report that
identifies agents, substances, mixtures, or exposures (collectively
called ``substances'') in our environment that may put people in the
United States at increased risk for cancer. The NTP prepares the RoC on
behalf of the Secretary of Health and Human Services.
The NTP follows an established, four-part process for preparation
of the RoC (https://ntp.niehs.nih.gov/go/rocprocess). A RoC Monograph is
prepared for each candidate substance selected for review for the RoC.
1-Bromopropane and cumene were selected as candidate substances
following solicitation of public comment and review by the NTP Board of
Scientific Counselors review on June 21-22, 2012 (https://ntp.niehs.nih.gov/go/9741). A draft RoC monograph consists of a (1)
cancer evaluation component that reviews all information that may bear
on a listing decision, assesses its quality and sufficiency for
reaching a listing decision, applies the RoC listing criteria to the
relevant scientific information, and recommends a listing status for
the candidate substance in the RoC and (2) a substance profile that
contains the NTP's preliminary listing recommendation and a summary of
the scientific evidence considered key to reaching that recommendation.
This meeting is planned for peer review of the draft RoC Monographs for
1-bromopropane and cumene.
1-Bromopropane (CASRN 106-94-5) is a brominated hydrocarbon that is
currently used as a solvent in a variety of industrial and commercial
applications. It is used as a solvent cleaner to degrease electronics,
precision optics, and metals, as a solvent vehicle in industries that
use aerosolized adhesives (e.g., foam cushion manufacturing), as a spot
remover in the textile industry, and as a solvent in the dry cleaning
industry. Additional information about the review of 1-bromopropane for
the RoC is available at https://ntp.niehs.nih.gov/go/37896.
Cumene (CASRN 98-82-8, isopropylbenzene) is an alkylated benzene
found in fossil fuels, such as blended gasoline and kerosene, and
products of incomplete combustion. It is a high production volume
chemical in the United States with the majority of its use in the
synthesis of acetone and phenol. Additional information about the
review of cumene for the RoC is available at https://ntp.niehs.nih.gov/go/37895.
Meeting and Registration: The meeting is open to the public with
time set aside for oral public comment; attendance at the NIEHS is
limited only by the space available. The meeting is scheduled for March
21, 2013, 1:00 p.m. to approximately 5:00 p.m. EDT and March 22, 2013,
from 8:30 a.m. until adjournment, approximately 2:00 p.m. EDT. Two days
are set aside for the meeting; however, it may adjourn sooner if the
panel completes its peer review of the draft monographs. Pre-
registration to attend the meeting and/or provide oral comments is by
March 19, 2013, at https://ntp.niehs.nih.gov/go/36639. Visitor and
security information is available at https://www.niehs.nih.gov/about/visiting/index.cfm. Individuals with disabilities who need
accommodation to participate in this event should contact Danica
Andrews at phone: (919) 541-2595 or email: andrewsda@niehs.nih.gov. TTY
users should contact the Federal TTY Relay Service at (800) 877-8339.
Requests should be made at least five business days in advance of the
event.
The preliminary agenda and draft monographs should be posted on the
NTP Web site (https://ntp.niehs.nih.gov/go/36639) by January 23, 2013.
Additional information will be posted when available or may be
requested in hardcopy, see FOR FURTHER INFORMATION CONTACT. Following
the meeting, a report of the peer review will be prepared and made
available on the NTP Web site. Registered attendees are encouraged to
access the meeting Web page to stay abreast of the most current
information regarding the meeting.
Request for Comments: The NTP invites written and oral public
comments on the draft monographs. The deadline for submission of
written comments is March 7, 2013, to enable review by the peer review
panel and NTP staff prior to the meeting. Pre-registration to provide
oral comments is by March 19, 2013, at https://ntp.niehs.nih.gov/go/36639. Public comments and any other correspondence on the draft
monographs should be sent to the FOR FURTHER INFORMATION CONTACT.
Persons submitting written comments should include their name,
affiliation, mailing address, phone, email, and sponsoring organization
(if any) with the document. Written comments received in response to
this notice will be posted on the NTP Web site, and the submitter will
be identified by name, affiliation, and/or sponsoring organization.
Public comment at this meeting is welcome, with time set aside for
the presentation of oral comments on the draft monographs. In addition
to in-person oral comments at the meeting at the NIEHS, public comments
can be presented by teleconference line. There will be 50 lines for
this call; availability will be on a first-come, first-served basis.
The lines will be open from 1:00 p.m. until approximately 5:00 p.m. EDT
on March 21 and from 8:30 a.m. EDT until adjournment on March 22,
although oral comments will be received only during the formal public
comment periods indicated on the preliminary agenda. Each organization
is allowed one time slot. At least 7 minutes will be allotted to each
speaker, and if time permits, may be extended to 10 minutes at the
discretion of the chair. Persons wishing to make an oral presentation
are asked to register online at https://ntp.niehs.nih.gov/go/36639 by
March 19, 2013, and if possible, to send a copy of their slides and/or
statement or talking points at that time. Written statements can
supplement and may expand the oral presentation. Registration for oral
comments will also be available at the meeting, although time allowed
for presentation by on-site registrants may be less than that for pre-
registered speakers and will be determined by the number of speakers
who register on-site.
Background Information on the RoC: Published biennially, each
edition of the RoC is cumulative and consists of substances newly
reviewed in addition to those listed in previous editions. The 12th
RoC, the latest edition, was published on June 10, 2011 (available at
[[Page 4421]]
https://ntp.niehs.nih.gov/go/roc12). The 13th RoC is under development.
For each listed substance, the RoC contains a substance profile, which
provides information on: Cancer studies that support the listing--
including those in humans, animals, and studies on possible mechanisms
of action--information about potential sources of exposure to humans,
and current Federal regulations to limit exposures.
Background Information on NTP Peer Review Panels: NTP panels are
technical, scientific advisory bodies established on an ``as needed''
basis to provide independent scientific peer review and advise the NTP
on agents of public health concern, new/revised toxicological test
methods, or other issues. These panels help ensure transparent,
unbiased, and scientifically rigorous input to the program for its use
in making credible decisions about human hazard, setting research and
testing priorities, and providing information to regulatory agencies
about alternative methods for toxicity screening. The NTP welcomes
nominations of scientific experts for upcoming panels. Scientists
interested in serving on an NTP panel should provide a current
curriculum vitae to the FOR FURTHER INFORMATION CONTACT. The authority
for NTP panels is provided by 42 U.S.C. 217a; section 222 of the Public
Health Service (PHS) Act, as amended. The panel is governed by the
Federal Advisory Committee Act, as amended (5 U.S.C. Appendix 2), which
sets forth standards for the formation and use of advisory committees.
Dated: January 16, 2013.
John R. Bucher,
Associate Director, National Toxicology Program.
[FR Doc. 2013-01242 Filed 1-18-13; 8:45 am]
BILLING CODE 4140-01-P