National Toxicology Program (NTP) Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM): Workshop Series on Best Practices for Regulatory Safety Testing: Assessing the Potential for Chemically Induced Eye Injuries and Chemically Induced Allergic Contact Dermatitis (ACD), 62845-62847 [2010-25676]
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Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Notices
a hospital-based environment, where
the risks to the patient are minimized.
CDRH and NIH seek feedback on ways
to overcome obstacles in the
development of an artificial pancreas
and what might be considered
reasonable clinical expectations for
systems considering the available
existing technology.
This public workshop is to seek input
from a wide range of constituencies
including but not be limited to industry,
academia, patient/consumer advocacy
groups, professional organizations, and
other State and Federal bodies under
aligned public health missions, to
address the issues outlined in this
notice. During the public workshop,
there will be an open dialogue between
Federal Government and experts from
the private and public sectors regarding
the topics described in this document.
Workshop participants will not be
expected to develop consensus
recommendations, but rather to provide
their perspectives on the clinical
development of these device systems.
II. Issues for Discussion
The workshop will focus on three
topics: (1) Technical considerations
when developing a clinical study
design; (2) expectations of the various
artificial pancreas device systems; and
(3) a discussion of the various
development plans for the Artificial
Pancreas System. The discussion of
these general topics should not be
limited by current statutes or
regulations and will include, but not be
limited to, discussion of the preceding
questions.
mstockstill on DSKH9S0YB1PROD with NOTICES
III. Where can I find more information
about this public workshop?
Background information on the public
workshop, registration information, the
agenda, and other relevant information
will be posted, as it becomes available,
on the Internet at https://www.fda.gov/
MedicalDevices/NewsEvents/
WorkshopsConferences/
ucm226251.htm.
IV. Transcripts
Please be advised that as soon as a
transcript is available, it will be
accessible at https://
www.regulations.gov. It may be viewed
at the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD. A transcript will
also be available in either hardcopy or
on CD–ROM, after submission of a
Freedom of Information request. Written
requests are to be sent to Division of
Freedom of Information (HFI–35), Office
of Management Programs, Food and
VerDate Mar<15>2010
17:22 Oct 12, 2010
Jkt 223001
Drug Administration, 5600 Fishers
Lane, Rm. 6–30, Rockville, MD 20857.
Dated: October 5, 2010.
Nancy K. Stade,
Deputy Director for Policy, Center for Devices
and Radiological Health.
[FR Doc. 2010–25600 Filed 10–12–10; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Toxicology Program (NTP)
Interagency Center for the Evaluation
of Alternative Toxicological Methods
(NICEATM): Workshop Series on Best
Practices for Regulatory Safety
Testing: Assessing the Potential for
Chemically Induced Eye Injuries and
Chemically Induced Allergic Contact
Dermatitis (ACD)
National Institute of
Environmental Health Sciences
(NIEHS), National Institutes of Health
(NIH), Department of Health and Human
Services.
ACTION: Announcement of a Workshop
Series.
AGENCY:
NICEATM and the
Interagency Coordinating Committee on
the Validation of Alternative Methods
(ICCVAM) announce a planned series of
workshops on ‘‘Best Practices for
Regulatory Safety Testing.’’ The first two
workshops in this series, ‘‘Best Practices
for Assessing the Potential for
Chemically Induced Eye Injuries’’ and
‘‘Best Practices for Assessing the
Potential for Chemically Induced
Allergic Contact Dermatitis,’’ are
planned for January 19 and 20, 2011,
respectively. These one-day workshops
will help participants gain a practical
understanding of the theory and
application of available in vitro and in
vivo alternative test methods that can be
used to evaluate the hazard potential of
chemicals and products while avoiding
or minimizing animal use and animal
pain and distress. Participants will learn
the strengths and weaknesses of
available alternative test methods,
become familiar with the types of data
they provide, and learn how to use these
data in regulatory safety assessments.
Workshop topics will be of particular
interest to those involved in conducting
safety tests for chemically induced eye
injuries and/or chemically induced
ACD, those responsible for reviewing
and approving study protocols prior to
testing, and regulators who are expected
to review data generated by the tests.
The workshops are free and open to the
SUMMARY:
PO 00000
Frm 00091
Fmt 4703
Sfmt 4703
62845
public with attendance limited only by
the space available. Those interested
may register for one or both workshops.
DATES: The workshop on ‘‘Assessing the
Potential for Chemically Induced Eye
Injuries’’ will be held on January 19,
2011. The workshop on ‘‘Assessing the
Potential for Chemically Induced
Allergic Contact Dermatitis’’ will be held
on January 20, 2011. Sessions for both
workshops will begin at 8:30 a.m. and
end at approximately 5 p.m. Individuals
who plan to attend either or both
workshops are asked to register with
NICEATM by January 6, 2011.
ADDRESSES: The workshops will be held
at the William H. Natcher Conference
Center, 45 Center Drive, NIH Campus,
Bethesda, MD 20892. Persons needing
special assistance in order to attend,
such as sign language interpretation or
other reasonable accommodation,
should contact 919–541–2475 voice,
919–541–4644 TTY (text telephone),
through the Federal TTY Relay System
at 800–877–8339, or e-mail to
niehsoeeo@niehs.nih.gov. Requests
should be made at least 14 days before
the event.
FOR FURTHER INFORMATION CONTACT:
Correspondence should be sent by mail,
fax, or e-mail to Dr. William S. Stokes,
NICEATM Director, NIEHS, P.O. Box
12233, MD K2–16, Research Triangle
Park, NC 27709, (phone) 919–541–2384,
(fax) 919–541–0947, (e-mail)
niceatm@niehs.nih.gov.
SUPPLEMENTARY INFORMATION:
Background
To protect workers and consumers,
regulatory agencies require testing to
determine if chemicals and products
may cause illnesses or injuries. Each
year, approximately 2 million eye
injuries occur in the U.S., of which
more than 40,000 result in permanent
visual impairment. Data on consumer
product-related eye injuries indicate
that the most common products causing
eye injuries in children under the age of
10 are household cleaning chemicals
and other chemical products. ACD is
also a significant concern because skin
diseases, including ACD, constitute the
second most common category of
occupational disease. ACD frequently
develops in workers and consumers
exposed to skin sensitizing products
and chemicals, results in lost workdays,
and can significantly diminish quality
of life.
To address these concerns, regulatory
authorities require safety testing that
can identify substances that may present
these hazards. Tests for ocular and ACD
hazards are two of the four most
frequently conducted product safety
E:\FR\FM\13OCN1.SGM
13OCN1
mstockstill on DSKH9S0YB1PROD with NOTICES
62846
Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Notices
tests. Test results are used to determine
appropriate labeling to warn consumers
and workers of potential hazards and to
communicate precautions that should
be taken to avoid eye injury or
development of ACD.
The U.S. Public Health Service Policy
on Humane Care and Use of Laboratory
Animals and the U.S. Department of
Agriculture’s Animal Welfare Act
regulations 1 require that alternatives to
procedures that can cause more than
slight or momentary pain or distress to
test animals must be considered and
used where appropriate. Substantial
progress has been made in recent years
in the development, validation, and
regulatory acceptance of alternative test
methods that reduce, refine (decrease or
eliminate pain and distress), or replace
the use of animals for ocular safety
assessments and ACD hazard testing.
Investigators and Institutional Animal
Care and Use Committee (IACUC)
members need to be aware of currently
available alternative methods so that
they can be considered before animal
study protocols are approved.
For ocular safety testing, ICCVAM has
recommended the bovine corneal
opacity and permeability, isolated
chicken eye, and Cytosensor
microphysiometer test methods for use
in specific circumstances to identify
ocular corrosives and severe irritants
without the use of live animals.
ICCVAM also recently recommended
that pain management procedures
should always be used whenever it is
necessary to use rabbits for eye safety
testing required by Federal regulatory
agencies. The ICCVAM
recommendations include a test method
protocol that describes how to use
topical anesthetics (similar to those
used in human eye surgeries) and
systemic analgesics prior to and after
test substance administration in order to
avoid or minimize animal pain and
distress. The report also identifies
specific clinical signs and lesions that,
if observed during animal testing, can be
used as humane endpoints to allow the
investigator to end a study early in order
to reduce or avoid potential animal pain
and distress. Use of the ICCVAMrecommended ocular safety testing
methods (available at https://
iccvam.niehs.nih.gov/methods/ocutox/
ocutox.htm) may reduce the number of
animals required to identify substances
with the potential to cause chemically
induced eye injuries, and eliminate pain
and distress when it is necessary to use
animals for such testing.
To identify substances with the
potential to cause ACD, U.S. Federal
17
U.S.C. 2131–2159.
VerDate Mar<15>2010
17:22 Oct 12, 2010
Jkt 223001
agencies have accepted ICCVAM
recommendations on an updated
murine local lymph node assay (LLNA)
protocol that uses 20% fewer animals.
Federal agencies also accepted ICCVAM
recommendations on the use of a
modified procedure called the reduced
LLNA that uses 40% fewer animals than
the updated 3-dose LLNA protocol.
ICCVAM also recently recommended
two modified versions of the LLNA that
do not require radioactive reagents,
allowing more institutions to take
advantage of the reduction and
refinement benefits afforded by the
LLNA compared to traditional guinea
pig methods. These nonradioactive
methods will also eliminate the expense
and environmental hazard associated
with use and disposal of radioactive
materials used in the traditional LLNA.
ICCVAM-recommended ACD testing
methods are available at https://
iccvam.niehs.nih.gov/methods/
immunotox/immunotox.htm.
While toxicologists recognize the
usefulness and strengths of these new
approaches, many are unfamiliar with
the specific techniques. Before a new
test method is implemented, the safety
community must understand the
method, as well as the manner in which
agencies expect the method to be
conducted and data interpreted. Users
and regulatory agency staff need to
become familiar with the technical
procedures required to conduct a new
method, and to understand the method’s
usefulness and limitations.
Consequently, there is a need for indepth training of individuals in the
safety and regulatory community on the
appropriate use of new tools for hazard,
safety, and risk assessment.
These workshops provide
opportunities for such training. They
will bring together scientific experts
from relevant stakeholder organizations
to discuss available alternative test
methods for assessing chemicals and
products for their ocular and ACD
hazard potential. The goal is to raise
awareness of available alternatives that
users should consider before using
traditional animal methods to assess eye
injury and ACD hazards. The workshops
will also provide information about the
usefulness and limitations of these test
methods. Users can then determine
whether the methods are appropriate for
specific testing applications.
Who Should Attend
Scientists from industry, government,
and academia who have an interest in
learning more about alternative test
methods that are available for assessing
potential eye injury or ACD hazards are
encouraged to participate. Topics
PO 00000
Frm 00092
Fmt 4703
Sfmt 4703
discussed during these workshops will
be of particular interest to those
involved in conducting tests for ocular
safety and ACD hazards (such as
toxicologists and study directors), those
responsible for reviewing study
protocols prior to testing (such as
chairpersons and members of IACUCs),
and regulators who will review data
generated by such tests. Those
interested may choose to attend one or
both workshops.
Workshop Program
The workshop on ‘‘Best Practices for
Assessing the Potential for Chemically
Induced Eye Injuries’’ will be held on
January 19, 2011. The workshop on
‘‘Best Practices for Assessing the
Potential for Chemically Induced
Allergic Contact Dermatitis’’ will
convene on January 20, 2011. Sessions
are scheduled to run from 8:30 a.m. to
5 p.m. each day. The programs will
begin with presentations on U.S.
requirements for the consideration of
available alternatives, current regulatory
requirements for safety testing, and the
acceptance status of alternative
methods. The scientific development of
the test methods will be described, and
the validation status of the test methods
will be discussed. Detailed
presentations will then provide
practical instruction on application of
the test methods, including standard
protocols and data interpretation.
Workshop participants will also have an
opportunity to apply knowledge gained
from the program using case studies in
breakout group discussion sessions.
Preliminary Workshop Agenda: Best
Practices for Assessing the Potential for
Chemically Induced Eye Injuries
(January 19, 2011)
• Welcome, Introduction, and Public
Health Impact of Chemically Induced
Eye Injuries.
• Review of Alternative Test Methods
and Integrated Strategies for Ocular
Safety Assessments.
• Consideration and Use of Available
Reduction, Refinement, and
Replacement Alternative Test Methods:
Study Director and IACUC
Responsibilities.
• Current Guidelines for Ocular
Safety Testing.
• Regulatory Agency Requirements
and Acceptable Alternative Test
Methods for Ocular Safety Assessments.
• ICCVAM Evaluation and
Recommendations on Best Practices for
Incorporating Pain Management and
Humane Endpoints in Ocular Safety
Testing.
• The Bovine Corneal Opacity and
Permeability Test Method.
E:\FR\FM\13OCN1.SGM
13OCN1
Federal Register / Vol. 75, No. 197 / Wednesday, October 13, 2010 / Notices
• The Isolated Chicken Eye Test
Method.
• The Cytosensor Microphysiometer
Test Method.
• Case Studies in Breakout Groups.
• New Models and Strategies in the
Validation Pipeline for Ocular Safety
Testing.
• Roundtable Discussion and
Summary Question-and-Answer
Session.
• Closing Comments.
Preliminary Workshop Agenda: Best
Practices for Assessing the Potential for
Chemically Induced Allergic Contact
Dermatitis (January 20, 2011)
• Welcome, Introduction, and Public
Health Impact of Chemically Induced
ACD.
• Review of Alternative Test Methods
and Integrated Strategies for ACD
Hazard Assessments.
• Consideration and Use of Available
Reduction, Refinement, and
Replacement Alternative Test Methods:
Study Director and IACUC
Responsibilities.
• Current Guidelines for ACD Hazard
Testing.
• Regulatory Agency Requirements
and Acceptable Alternative Test
Methods for ACD Hazard Assessments.
• The Reduced LLNA.
• The LLNA: Bromodeoxyuridine
Enzyme-linked Immunosorbent Assay
(BrdU–ELISA).
• The LLNA: Daicel Adenosine
Triphosphate (DA).
• Application of Peptide Reactivity
for Screening ACD Hazard Potential.
• Case Studies in Breakout Groups.
• New Models and Strategies in the
Validation Pipeline for ACD Hazard
Testing.
• Roundtable Discussion and
Summary Question-and-Answer
Session.
• Closing Comments.
Registration
mstockstill on DSKH9S0YB1PROD with NOTICES
Registration information, a tentative
agenda for each workshop, and
additional information for both
workshops are available on the
NICEATM–ICCVAM Web site (https://
iccvam.niehs.nih.gov/meetings/
Implement-2011/ImplmtnWksp.htm)
and upon request from NICEATM (see
FOR FURTHER INFORMATION CONTACT).
Background Information on ICCVAM
and NICEATM
ICCVAM is an interagency committee
composed of representatives from 15
U.S. Federal regulatory and research
agencies that require, use, or generate
toxicological and safety testing
information for chemicals, products,
VerDate Mar<15>2010
17:22 Oct 12, 2010
Jkt 223001
and other substances. ICCVAM
conducts technical evaluations of new,
revised, and alternative methods with
regulatory applicability, and promotes
the scientific validation, regulatory
acceptance, and national and
international harmonization of
toxicological and safety testing methods
that more accurately assess the safety
and health hazards of chemicals and
products while reducing, refining
(decreasing or eliminating pain and
distress), or replacing animal use. The
ICCVAM Authorization Act of 2000 (42
U.S.C. 285l-2, 285l-5 [2000], available at
https://iccvam.niehs.nih.gov/docs/
about_docs/PL106545.pdf) established
ICCVAM as a permanent interagency
committee of the NIEHS under
NICEATM.
NICEATM administers ICCVAM,
provides scientific and operational
support for ICCVAM-related activities,
and coordinates international validation
studies of new and improved test
methods. NICEATM and ICCVAM work
collaboratively to evaluate new and
improved test methods applicable to the
needs of U.S. Federal agencies.
NICEATM and ICCVAM welcome the
public nomination of new, revised, and
alternative test methods for validation
studies as well as technical evaluations.
Additional information about NICEATM
and ICCVAM can be found on the
NICEATM–ICCVAM Web site (https://
www.iccvam.niehs.nih.gov).
Dated: October 1, 2010.
John R. Bucher,
Associate Director, National Toxicology
Program.
[FR Doc. 2010–25676 Filed 10–12–10; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
Notice of Issuance of Final
Determination Concerning an
ADFLOTM Respiration System
U.S. Customs and Border
Protection, Department of Homeland
Security.
ACTION: Notice of final determination.
AGENCY:
This document provides
notice that U.S. Customs and Border
Protection (‘‘CBP’’) has issued a final
determination concerning the country of
origin of an AdfloTM Respiration System
used in a welding environment. Based
upon the facts presented, CBP has
concluded in the final determination
that Sweden is the country of origin of
the AdfloTM Respiration System for
SUMMARY:
PO 00000
Frm 00093
Fmt 4703
Sfmt 4703
62847
purposes of U.S. government
procurement.
The final determination was
issued on October 6, 2010. A copy of the
final determination is attached. Any
party-at-interest, as defined in 19 CFR
177.22(d), may seek judicial review of
this final determination on or before
November 12, 2010.
DATES:
FOR FURTHER INFORMATION CONTACT:
Robert Dinerstein, Valuation and
Special Programs Branch: (202) 325–
0132.
Notice is
hereby given that on October 6, 2010,
pursuant to subpart B of part 177,
Customs Regulations (19 CFR part 177,
subpart B), CBP issued a final
determination concerning the country of
origin of the AdfloTM Respiration
System which may be offered to the U.S.
Government under an undesignated
government procurement contract. This
final determination, in HQ H112725,
was issued at the request of 3M
Company, Inc. under procedures set
forth at 19 CFR part 177, subpart B,
which implements Title III of the Trade
Agreements Act of 1979, as amended
(19 U.S.C. 2511–18). In the final
determination, CBP has concluded that,
based upon the facts presented and
precedent from the Court of
International Trade in Uniden America
Corporation v. United States, 120. Supp.
2d. 1091, (Ct. Int’l Trade 2000), that a
battery charger included with the
AdfloTM System, lost its separate
identity and became part of the system
rendering Sweden the country of origin
of the AdfloTM Respiration System for
purposes of U.S. government
procurement. With respect to a cloth bag
enclosed with the AdfloTM respiration
system, because it is a textile product,
we indicated that its country of origin
is to be determined in accordance with
rules for the country of origin of textile
products set forth in 19 U.S.C. 3592 and
CBP Regulations at 19 CFR 102.21.
Since we did not have enough
information, we could not rule on the
country of origin of the bag.
Section 177.29, Customs Regulations
(19 CFR 177.29), provides that notice of
final determinations shall be published
in the Federal Register within 60 days
of the date the final determination is
issued. Section 177.30, CBP Regulations
(19 CFR 177.30), provides that any
party-at-interest, as defined in 19 CFR
177.22(d), may seek judicial review of a
final determination within 30 days of
publication of such determination in the
Federal Register.
SUPPLEMENTARY INFORMATION:
E:\FR\FM\13OCN1.SGM
13OCN1
Agencies
[Federal Register Volume 75, Number 197 (Wednesday, October 13, 2010)]
[Notices]
[Pages 62845-62847]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-25676]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Toxicology Program (NTP) Interagency Center for the
Evaluation of Alternative Toxicological Methods (NICEATM): Workshop
Series on Best Practices for Regulatory Safety Testing: Assessing the
Potential for Chemically Induced Eye Injuries and Chemically Induced
Allergic Contact Dermatitis (ACD)
AGENCY: National Institute of Environmental Health Sciences (NIEHS),
National Institutes of Health (NIH), Department of Health and Human
Services.
ACTION: Announcement of a Workshop Series.
-----------------------------------------------------------------------
SUMMARY: NICEATM and the Interagency Coordinating Committee on the
Validation of Alternative Methods (ICCVAM) announce a planned series of
workshops on ``Best Practices for Regulatory Safety Testing.'' The
first two workshops in this series, ``Best Practices for Assessing the
Potential for Chemically Induced Eye Injuries'' and ``Best Practices
for Assessing the Potential for Chemically Induced Allergic Contact
Dermatitis,'' are planned for January 19 and 20, 2011, respectively.
These one-day workshops will help participants gain a practical
understanding of the theory and application of available in vitro and
in vivo alternative test methods that can be used to evaluate the
hazard potential of chemicals and products while avoiding or minimizing
animal use and animal pain and distress. Participants will learn the
strengths and weaknesses of available alternative test methods, become
familiar with the types of data they provide, and learn how to use
these data in regulatory safety assessments. Workshop topics will be of
particular interest to those involved in conducting safety tests for
chemically induced eye injuries and/or chemically induced ACD, those
responsible for reviewing and approving study protocols prior to
testing, and regulators who are expected to review data generated by
the tests. The workshops are free and open to the public with
attendance limited only by the space available. Those interested may
register for one or both workshops.
DATES: The workshop on ``Assessing the Potential for Chemically Induced
Eye Injuries'' will be held on January 19, 2011. The workshop on
``Assessing the Potential for Chemically Induced Allergic Contact
Dermatitis'' will be held on January 20, 2011. Sessions for both
workshops will begin at 8:30 a.m. and end at approximately 5 p.m.
Individuals who plan to attend either or both workshops are asked to
register with NICEATM by January 6, 2011.
ADDRESSES: The workshops will be held at the William H. Natcher
Conference Center, 45 Center Drive, NIH Campus, Bethesda, MD 20892.
Persons needing special assistance in order to attend, such as sign
language interpretation or other reasonable accommodation, should
contact 919-541-2475 voice, 919-541-4644 TTY (text telephone), through
the Federal TTY Relay System at 800-877-8339, or e-mail to
niehsoeeo@niehs.nih.gov. Requests should be made at least 14 days
before the event.
FOR FURTHER INFORMATION CONTACT: Correspondence should be sent by mail,
fax, or e-mail to Dr. William S. Stokes, NICEATM Director, NIEHS, P.O.
Box 12233, MD K2-16, Research Triangle Park, NC 27709, (phone) 919-541-
2384, (fax) 919-541-0947, (e-mail) niceatm@niehs.nih.gov.
SUPPLEMENTARY INFORMATION:
Background
To protect workers and consumers, regulatory agencies require
testing to determine if chemicals and products may cause illnesses or
injuries. Each year, approximately 2 million eye injuries occur in the
U.S., of which more than 40,000 result in permanent visual impairment.
Data on consumer product-related eye injuries indicate that the most
common products causing eye injuries in children under the age of 10
are household cleaning chemicals and other chemical products. ACD is
also a significant concern because skin diseases, including ACD,
constitute the second most common category of occupational disease. ACD
frequently develops in workers and consumers exposed to skin
sensitizing products and chemicals, results in lost workdays, and can
significantly diminish quality of life.
To address these concerns, regulatory authorities require safety
testing that can identify substances that may present these hazards.
Tests for ocular and ACD hazards are two of the four most frequently
conducted product safety
[[Page 62846]]
tests. Test results are used to determine appropriate labeling to warn
consumers and workers of potential hazards and to communicate
precautions that should be taken to avoid eye injury or development of
ACD.
The U.S. Public Health Service Policy on Humane Care and Use of
Laboratory Animals and the U.S. Department of Agriculture's Animal
Welfare Act regulations \1\ require that alternatives to procedures
that can cause more than slight or momentary pain or distress to test
animals must be considered and used where appropriate. Substantial
progress has been made in recent years in the development, validation,
and regulatory acceptance of alternative test methods that reduce,
refine (decrease or eliminate pain and distress), or replace the use of
animals for ocular safety assessments and ACD hazard testing.
Investigators and Institutional Animal Care and Use Committee (IACUC)
members need to be aware of currently available alternative methods so
that they can be considered before animal study protocols are approved.
---------------------------------------------------------------------------
\1\ 7 U.S.C. 2131-2159.
---------------------------------------------------------------------------
For ocular safety testing, ICCVAM has recommended the bovine
corneal opacity and permeability, isolated chicken eye, and Cytosensor
microphysiometer test methods for use in specific circumstances to
identify ocular corrosives and severe irritants without the use of live
animals. ICCVAM also recently recommended that pain management
procedures should always be used whenever it is necessary to use
rabbits for eye safety testing required by Federal regulatory agencies.
The ICCVAM recommendations include a test method protocol that
describes how to use topical anesthetics (similar to those used in
human eye surgeries) and systemic analgesics prior to and after test
substance administration in order to avoid or minimize animal pain and
distress. The report also identifies specific clinical signs and
lesions that, if observed during animal testing, can be used as humane
endpoints to allow the investigator to end a study early in order to
reduce or avoid potential animal pain and distress. Use of the ICCVAM-
recommended ocular safety testing methods (available at https://iccvam.niehs.nih.gov/methods/ocutox/ocutox.htm) may reduce the number
of animals required to identify substances with the potential to cause
chemically induced eye injuries, and eliminate pain and distress when
it is necessary to use animals for such testing.
To identify substances with the potential to cause ACD, U.S.
Federal agencies have accepted ICCVAM recommendations on an updated
murine local lymph node assay (LLNA) protocol that uses 20% fewer
animals. Federal agencies also accepted ICCVAM recommendations on the
use of a modified procedure called the reduced LLNA that uses 40% fewer
animals than the updated 3-dose LLNA protocol. ICCVAM also recently
recommended two modified versions of the LLNA that do not require
radioactive reagents, allowing more institutions to take advantage of
the reduction and refinement benefits afforded by the LLNA compared to
traditional guinea pig methods. These nonradioactive methods will also
eliminate the expense and environmental hazard associated with use and
disposal of radioactive materials used in the traditional LLNA. ICCVAM-
recommended ACD testing methods are available at https://iccvam.niehs.nih.gov/methods/immunotox/immunotox.htm.
While toxicologists recognize the usefulness and strengths of these
new approaches, many are unfamiliar with the specific techniques.
Before a new test method is implemented, the safety community must
understand the method, as well as the manner in which agencies expect
the method to be conducted and data interpreted. Users and regulatory
agency staff need to become familiar with the technical procedures
required to conduct a new method, and to understand the method's
usefulness and limitations. Consequently, there is a need for in-depth
training of individuals in the safety and regulatory community on the
appropriate use of new tools for hazard, safety, and risk assessment.
These workshops provide opportunities for such training. They will
bring together scientific experts from relevant stakeholder
organizations to discuss available alternative test methods for
assessing chemicals and products for their ocular and ACD hazard
potential. The goal is to raise awareness of available alternatives
that users should consider before using traditional animal methods to
assess eye injury and ACD hazards. The workshops will also provide
information about the usefulness and limitations of these test methods.
Users can then determine whether the methods are appropriate for
specific testing applications.
Who Should Attend
Scientists from industry, government, and academia who have an
interest in learning more about alternative test methods that are
available for assessing potential eye injury or ACD hazards are
encouraged to participate. Topics discussed during these workshops will
be of particular interest to those involved in conducting tests for
ocular safety and ACD hazards (such as toxicologists and study
directors), those responsible for reviewing study protocols prior to
testing (such as chairpersons and members of IACUCs), and regulators
who will review data generated by such tests. Those interested may
choose to attend one or both workshops.
Workshop Program
The workshop on ``Best Practices for Assessing the Potential for
Chemically Induced Eye Injuries'' will be held on January 19, 2011. The
workshop on ``Best Practices for Assessing the Potential for Chemically
Induced Allergic Contact Dermatitis'' will convene on January 20, 2011.
Sessions are scheduled to run from 8:30 a.m. to 5 p.m. each day. The
programs will begin with presentations on U.S. requirements for the
consideration of available alternatives, current regulatory
requirements for safety testing, and the acceptance status of
alternative methods. The scientific development of the test methods
will be described, and the validation status of the test methods will
be discussed. Detailed presentations will then provide practical
instruction on application of the test methods, including standard
protocols and data interpretation. Workshop participants will also have
an opportunity to apply knowledge gained from the program using case
studies in breakout group discussion sessions.
Preliminary Workshop Agenda: Best Practices for Assessing the Potential
for Chemically Induced Eye Injuries (January 19, 2011)
Welcome, Introduction, and Public Health Impact of
Chemically Induced Eye Injuries.
Review of Alternative Test Methods and Integrated
Strategies for Ocular Safety Assessments.
Consideration and Use of Available Reduction, Refinement,
and Replacement Alternative Test Methods: Study Director and IACUC
Responsibilities.
Current Guidelines for Ocular Safety Testing.
Regulatory Agency Requirements and Acceptable Alternative
Test Methods for Ocular Safety Assessments.
ICCVAM Evaluation and Recommendations on Best Practices
for Incorporating Pain Management and Humane Endpoints in Ocular Safety
Testing.
The Bovine Corneal Opacity and Permeability Test Method.
[[Page 62847]]
The Isolated Chicken Eye Test Method.
The Cytosensor Microphysiometer Test Method.
Case Studies in Breakout Groups.
New Models and Strategies in the Validation Pipeline for
Ocular Safety Testing.
Roundtable Discussion and Summary Question-and-Answer
Session.
Closing Comments.
Preliminary Workshop Agenda: Best Practices for Assessing the Potential
for Chemically Induced Allergic Contact Dermatitis (January 20, 2011)
Welcome, Introduction, and Public Health Impact of
Chemically Induced ACD.
Review of Alternative Test Methods and Integrated
Strategies for ACD Hazard Assessments.
Consideration and Use of Available Reduction, Refinement,
and Replacement Alternative Test Methods: Study Director and IACUC
Responsibilities.
Current Guidelines for ACD Hazard Testing.
Regulatory Agency Requirements and Acceptable Alternative
Test Methods for ACD Hazard Assessments.
The Reduced LLNA.
The LLNA: Bromodeoxyuridine Enzyme-linked Immunosorbent
Assay (BrdU-ELISA).
The LLNA: Daicel Adenosine Triphosphate (DA).
Application of Peptide Reactivity for Screening ACD Hazard
Potential.
Case Studies in Breakout Groups.
New Models and Strategies in the Validation Pipeline for
ACD Hazard Testing.
Roundtable Discussion and Summary Question-and-Answer
Session.
Closing Comments.
Registration
Registration information, a tentative agenda for each workshop, and
additional information for both workshops are available on the NICEATM-
ICCVAM Web site (https://iccvam.niehs.nih.gov/meetings/Implement-2011/ImplmtnWksp.htm) and upon request from NICEATM (see FOR FURTHER
INFORMATION CONTACT).
Background Information on ICCVAM and NICEATM
ICCVAM is an interagency committee composed of representatives from
15 U.S. Federal regulatory and research agencies that require, use, or
generate toxicological and safety testing information for chemicals,
products, and other substances. ICCVAM conducts technical evaluations
of new, revised, and alternative methods with regulatory applicability,
and promotes the scientific validation, regulatory acceptance, and
national and international harmonization of toxicological and safety
testing methods that more accurately assess the safety and health
hazards of chemicals and products while reducing, refining (decreasing
or eliminating pain and distress), or replacing animal use. The ICCVAM
Authorization Act of 2000 (42 U.S.C. 285l-2, 285l-5 [2000], available
at https://iccvam.niehs.nih.gov/docs/about_docs/PL106545.pdf)
established ICCVAM as a permanent interagency committee of the NIEHS
under NICEATM.
NICEATM administers ICCVAM, provides scientific and operational
support for ICCVAM-related activities, and coordinates international
validation studies of new and improved test methods. NICEATM and ICCVAM
work collaboratively to evaluate new and improved test methods
applicable to the needs of U.S. Federal agencies. NICEATM and ICCVAM
welcome the public nomination of new, revised, and alternative test
methods for validation studies as well as technical evaluations.
Additional information about NICEATM and ICCVAM can be found on the
NICEATM-ICCVAM Web site (https://www.iccvam.niehs.nih.gov).
Dated: October 1, 2010.
John R. Bucher,
Associate Director, National Toxicology Program.
[FR Doc. 2010-25676 Filed 10-12-10; 8:45 am]
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