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STALLED. UNDER-FUNDED. CRUEL.
Since the ICCVAM Authorization Act established the Interagency Coordinating Committee on the Validation of
Alternative Methods as a permanent committee in 2000, ICCVAM has approved just four non-animal tests (among
multiple reviews). Animals vomit, convulse, bleed and die in redundant experiments. Yet U.S. lawmakers stall
funds for ICCVAM to develop human-relevant models. ICCVAM's current committee clings to customary, but old-
fashioned animal experiments that haven't undergone thorough scientific analysis. Ask ICCVAM and lawmakers to
capitalize on strides in animal-free research technology. Remind ICCVAM to do its job. Demand that Congress enact
funding so ICCVAM can do its job.
THIS ALERT IS CLOSED. It is a live archive
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Dear Representative, Senators, and ICCVAM Committee:
The Lethal Dose 50 Percent (LD-50) test measures the dose of a substance needed to
kill half a group of laboratory animals. For up to two
years, animals ingest chemicals via stomach tube, inhalation, spray and injection.
They vomit, convulse, become paralyzed and bleed from
their eyes, nose and mouth.
LD-50 tests are not as accurate as combined human cell tests. Still, pharmaceutical,
chemical and consumer firms are required to poison
animals. Companies that conduct animal-free experiments in-house must ultimately kill
animals to meet regulatory qualifications.
I respectfully ask government regulators to accelerate validation of non-animal
research tools. I also ask my elected officials to advocate
legislation mandating the use of animal-free tests.
Since the ICCVAM Authorization Act established the Interagency Coordinating Committee
on the Validation of Alternative Methods as a
permanent committee in 2000, ICCVAM's interagency panel has approved just four non-
animal tests (among 185 reviews). Comparatively,
the European Center for the Evaluation of Alternative Methods (ECVAM) has 34 human-
focused methods in place, with 170 more under active
evaluation. In 1986 the European Commission stipulated use of animal-free tests
whenever feasible and later began a phase-out of animal
experiments for cosmetics.
U.S. lawmakers must allocate funds to ICCVAM so informed scientists can develop non-
animal models as their European counterpart does.
ICCVAM's current committee clings to customary, but old-fashioned animal experiments
that haven't undergone thorough scientific analysis.
Toxicity testing in animals is "expensive, time-consuming, uses animals in large
numbers, and it doesn't always work," says Francis Collins,
director of NIH's National Human Genome Research Institute. A National Academy of
Sciences report, "Toxicity Testing in the 21st Century,"
calls for non-animal methodology. According to the National Research Council, in
vitro strategy "would generate more-relevant data to
evaluate risks people face."
It is indisputably cruel to pour toxins into the clipped-open eyes of rabbits (Draize
eye irritancy) or smear corrosives over an animal's shaved
skin (skin absorption tests). Human safety data should not come from poisoning
animals (LD-50) or overdosing them with drugs while locked
in metal restraints (pyrogenicity tests).
Please capitalize on strides in biology and computer automation that let researchers
gauge toxicity more reliably. I urge ICCVAM to do its job. I
urge Congress to enact funding so ICCVAM can do its job.
Thank you,
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email addresses only
stokes@niehs.nih.gov,
iccvam@niehs.nih.gov,
mwind@cpsc.gov,
mohammed.mumtaz@cdc.hhs.gov,
khatlelid@cpsc.gov,
jmatheson@cpsc.gov,
Robert.Foster@OSD.Mil,
Patty.decot@OSD.Mil,
Peter.Schultheiss@det.amedd.army.m
il,
harry.salem@us.army.mil,
michael.kuperberg@science.doe.gov
,
marvin.stodolsky@science.doe.gov,
barnett_rattner@usgs.gov,
Sarah_Gerould@usgs.gov,
george.cushmac@dot.gov,
steve.hwang@rspa.dot.gov,
hamernik.karen@epa.gov,
rispin.amy@epa.gov,
preston.julian@epa.gov,
mccall.deborah@epa.gov,
mcmaster.suzanne@epa.gov,
smrchek.jerry@epa.gov,
suzanne.fitzpatrick@fda.hhs.gov,
lawrence.dhoostelaere@fda.hhs.gov
,
william.allaben@fda.hhs.gov,
david.hattan@fda.hhs.gov,
paul.howard@fda.hhs.gov
robert.bronaugh@fda.hhs.gov,
richard.mcfarland@fda.hhs.gov,
devaraya.jagannath@fda.hhs.gov,
ying.huang@fda.hhs.gov,
cecilia.aguila@fda.hhs.gov,
abigail.jacobs@fda.hhs.gov,
melvin.stratmeyer@fda.hhs.gov,
paul.brown@fda.hhs.gov,
polanda@mail.nih.gov,
kevin.howcroft@nih.hhs.gov,
tice@niehs.nih.gov,
chhabrar@niehs.nih.gov,
heindelj@niehs.nih.gov,
snyderm@od.nih.gov,
paul.nicolaysen@cdc.hhs.gov,
kmurali.rao@cdc.hhs.gov,
goshorj@nlm.nih.gov,
ahir.surender@dol.gov,
jodie.a.kulpa-
eddy@aphis.usda.gov,
betty.j.goldentyer@usda.gov
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full contact information
Dr. William Stokes, ICCVAM Executive Director & NICEATM Director
Interagency Coordinating Committee on the Validation of Alternative Methods
NIEHS, EC-17, P.O. Box 12233
Research Triangle Park, NC, 27709
ph: 919-541-7997; email: stokes@niehs.nih.gov, iccvam@niehs.nih.gov
SOURCE: iccvam.niehs.nih.gov/methods/m
ethods.htm
Marilyn L. Wind, Ph.D., Chair, ICCVAM
Deputy Associate Executive Director
Directorate for Health Sciences
U.S. Consumer Product Safety Commission
4330 East West Highway, Rm. 600
Bethesda, Maryland 20814
ph: 301-504-7246; email: mwind@cpsc.gov
SOURCE: iccvam.niehs.nih.gov/ab
out/agencies/ni_Reps.htm
The Honorable Representative [YOUR REP'S NAME]
U.S. House of Representatives; Washington, D.C. 20510
The Honorable Senators [YOUR 2 SENATORS' NAMES]
The U.S. Senate, U.S. Capitol Building; Washington, D.C. 20510
To identify your federal legislators and find contact info, try:
• Congress.org: www.Congress.org
• USA Senate: www.senate.gov
• USA House of Representatives: www.house.gov
• Congressional Switchboard: 202-224-3121
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