Notice of Availability of the Benchmark Dose Technical Guidance, 36533 [2012-14897]
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Federal Register / Vol. 77, No. 118 / Tuesday, June 19, 2012 / Notices
conference in the above-referenced
proceedings on Tuesday, July 17, 2012,
from 9:30 a.m. to 4:00 p.m. (EDT) in the
Commission Meeting Room at the
offices of the Federal Energy Regulatory
Commission, 888 First Street NE.,
Washington, DC 20426. Members of the
Commission may attend the conference,
which will also be open for the public
to attend. Advance registration is not
required, but is encouraged. We will
provide nametags for those who register
on or before July 10, 2012. Participants
may register at the following Web page:
https://www.ferc.gov/whats-new/
registration/small-generator-7-17-12form.asp.
The purpose of this conference is to
discuss issues related to a petition for
rulemaking recently submitted by the
Solar Energy Industries Association
(Docket No. RM12–10–000).
This conference is not intended to
address the substance of any particular
case pending before the Commission.
However, discussions at the conference
may address matters at issue in the
following Commission proceedings that
are either pending or within their
rehearing period: California
Independent System Operator
Corporation, Docket No. ER12–502–001
and Docket No. ER12–502–002; PJM
Interconnection, LLC, Docket No. ER12–
1177–001; California Independent
System Operator Corporation, Docket
No. ER12–1855–000.
Those interested in speaking at the
conference should notify the
Commission by close of business June
22, 2012, by completing an online form
identifying the topic(s) that they wish to
address: https://www.ferc.gov/whatsnew/registration/small-generator-7-1712-speaker-form.asp. Due to time
constraints, we may not be able to
accommodate all those interested in
speaking. The Commission will issue a
subsequent notice that will provide the
detailed agenda for the conference,
including panel speakers, and a
comment date for filing post-conference
comments.
The conference will be transcribed
and available by webcast. Transcripts
will be available immediately for a fee
from Ace Reporting Company (202–
347–3700 or 1–800–336–6646). A free
webcast of the technical conference in
this proceeding is also available.
Anyone with Internet access interested
in viewing this conference can do so by
navigating to the FERC Calendar of
Events at www.ferc.gov and locating this
event in the Calendar. The event will
contain a link to its webcast. The
Capitol Connection provides technical
support for the webcasts and offers the
option of listening to the conferences
VerDate Mar<15>2010
16:39 Jun 18, 2012
Jkt 226001
via phone-bridge for a fee. If you have
any questions, visit
www.CapitolConnection.org or call (703)
993–3100.
FERC conferences are accessible
under section 508 of the Rehabilitation
Act of 1973. For accessibility
accommodations please send an email
to accessibility@ferc.gov or call toll free
1–866–208–3372 (voice) or 202–208–
8659 (TTY), or send a fax to 202–208–
2106 with the required
accommodations.
For information related to the agenda,
please contact Leslie Kerr at
leslie.kerr@ferc.gov or (202) 502–8540.
For information related to logistics,
please contact Sarah McKinley at
sarah.mckinley@ferc.gov or (202)
502–8368.
Dated: June 13, 2012.
Kimberly D. Bose,
Secretary.
[FR Doc. 2012–14885 Filed 6–18–12; 8:45 am]
BILLING CODE 6717–01–P
ENVIRONMENTAL PROTECTION
AGENCY
[FRL–9688–7]
Notice of Availability of the Benchmark
Dose Technical Guidance
Environmental Protection
Agency (EPA).
ACTION: Notice of Availability.
AGENCY:
The U.S. Environmental
Protection Agency is announcing the
availability of Benchmark Dose
Technical Guidance (BMD). This
document was developed as part of an
agency-wide guidance development
program by a technical panel of the
EPA’s Risk Assessment Forum. Drafts
were peer reviewed internally by EPA
scientists and externally by experts from
academia, industry, and other federal
and state government agencies. When
appropriate, the EPA intends to use the
guidance prospectively in conducting
risk assessments.
ADDRESSES: The BMD document is
available electronically through the
EPA’s Web site at https://www.epa.gov/
raf/publications/benchmarkdose.htm.
FOR FURTHER INFORMATION CONTACT: Dr.
Michael W. Broder, Risk Assessment
Forum, Office of the Science Advisor
(8105R), U.S. Environmental Protection
Agency, 1200 Pennsylvania Avenue
NW., Washington, DC 20460; on
telephone number (202) 564–3393;
facsimile number (202) 564–2070; or
email broder.michael@epa.gov.
SUPPLEMENTARY INFORMATION: In support
of its mission to protect human health
SUMMARY:
PO 00000
Frm 00057
Fmt 4703
Sfmt 4703
36533
and the environment, the EPA routinely
conducts risk assessments on chemical
agents that may be toxic to humans. A
key component of the risk assessment
process involves evaluating the doseresponse relationship between exposure
to the agent and the observed effect. The
dose-response assessment is a two-step
process: (1) Defining a point of
departure (POD); and (2) extrapolating
from the POD for relevance to
environmental exposures. Traditionally,
the no observed adverse effect level
(NOAEL) or lowest observed adverse
effect level (LOAEL) methods were used
for establishing the POD for noncancer
endpoints. The BMD method gained
favor within the risk assessment
community over time because it
incorporates and conveys more
information than the NOAEL/LOAEL
methods. The EPA conducted
workshops and symposia about the
application of BMD methodology and
the development of relevant guidance.
The BMD document focuses on the
use of the BMD methodology for human
health risk assessments. The document
discusses computation of BMD values
and their confidence limits, data
requirements, dose-response
assessment, and reporting
recommendations that are specific to
BMD values. Although the EPA has
generated its own BMD software
(https://www.epa.gov/ncea/BMDS/
index.html), this document supports the
use of other relevant, well-documented
software packages.
Dated: June 6, 2012.
Glenn Paulson,
Science Advisor.
[FR Doc. 2012–14897 Filed 6–18–12; 8:45 am]
BILLING CODE 6560–50–P
ENVIRONMENTAL PROTECTION
AGENCY
[EPA–R01–OW–2012–0201, FRL–9688–9]
Massachusetts Marine Sanitation
Device Standard—Notice of
Determination
Environmental Protection
Agency (EPA).
ACTION: Notice of Determination.
AGENCY:
The Regional Administrator
of the Environmental Protection
Agency—New England Region, has
determined that adequate facilities for
the safe and sanitary removal and
treatment of sewage from all vessels are
reasonably available for the waters of
Dighton, Berkley, Freetown, Somerset,
Swansea, and Fall River collectively
termed Mount Hope Bay.
SUMMARY:
E:\FR\FM\19JNN1.SGM
19JNN1
Agencies
[Federal Register Volume 77, Number 118 (Tuesday, June 19, 2012)]
[Notices]
[Page 36533]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-14897]
=======================================================================
-----------------------------------------------------------------------
ENVIRONMENTAL PROTECTION AGENCY
[FRL-9688-7]
Notice of Availability of the Benchmark Dose Technical Guidance
AGENCY: Environmental Protection Agency (EPA).
ACTION: Notice of Availability.
-----------------------------------------------------------------------
SUMMARY: The U.S. Environmental Protection Agency is announcing the
availability of Benchmark Dose Technical Guidance (BMD). This document
was developed as part of an agency-wide guidance development program by
a technical panel of the EPA's Risk Assessment Forum. Drafts were peer
reviewed internally by EPA scientists and externally by experts from
academia, industry, and other federal and state government agencies.
When appropriate, the EPA intends to use the guidance prospectively in
conducting risk assessments.
ADDRESSES: The BMD document is available electronically through the
EPA's Web site at https://www.epa.gov/raf/publications/benchmarkdose.htm.
FOR FURTHER INFORMATION CONTACT: Dr. Michael W. Broder, Risk Assessment
Forum, Office of the Science Advisor (8105R), U.S. Environmental
Protection Agency, 1200 Pennsylvania Avenue NW., Washington, DC 20460;
on telephone number (202) 564-3393; facsimile number (202) 564-2070; or
email broder.michael@epa.gov.
SUPPLEMENTARY INFORMATION: In support of its mission to protect human
health and the environment, the EPA routinely conducts risk assessments
on chemical agents that may be toxic to humans. A key component of the
risk assessment process involves evaluating the dose-response
relationship between exposure to the agent and the observed effect. The
dose-response assessment is a two-step process: (1) Defining a point of
departure (POD); and (2) extrapolating from the POD for relevance to
environmental exposures. Traditionally, the no observed adverse effect
level (NOAEL) or lowest observed adverse effect level (LOAEL) methods
were used for establishing the POD for noncancer endpoints. The BMD
method gained favor within the risk assessment community over time
because it incorporates and conveys more information than the NOAEL/
LOAEL methods. The EPA conducted workshops and symposia about the
application of BMD methodology and the development of relevant
guidance.
The BMD document focuses on the use of the BMD methodology for
human health risk assessments. The document discusses computation of
BMD values and their confidence limits, data requirements, dose-
response assessment, and reporting recommendations that are specific to
BMD values. Although the EPA has generated its own BMD software (https://www.epa.gov/ncea/BMDS/), this document supports the use of
other relevant, well-documented software packages.
Dated: June 6, 2012.
Glenn Paulson,
Science Advisor.
[FR Doc. 2012-14897 Filed 6-18-12; 8:45 am]
BILLING CODE 6560-50-P