We are working to end the FDA’s animal testing with the FDA Modernization Act of 2021 to eliminate the requirement that all new drugs go through extensive rounds of animal testing. Animal testing is outmoded because, unlike human biology-based test methods, animals are unreliable predictors of human response, delaying treatments and cures to patients and driving up drug costs.
Revising FDA testing mandates will spare animals and save human lives.
We are working to eliminate the requirement in the Federal Food, Drug and Cosmetics Act of 1938 for animal testing as the only test method for any new drug development protocol. The pharmaceutical industry is burdened by outdated FDA statutes and regulations that bar the use of faster, cheaper, and more reliable test methods.
There is urgency to address the problem because between 90 and 95 percent of drugs found safe in preclinical tests fail during human clinical trials due to toxicities not predicted by traditional animal tests or because of lack of efficacy. This exposes the public to unacceptable risk and stifles the movement of life-saving drugs into the marketplace.
The broader results are extraordinarily high costs for drugs, inordinately long wait periods bringing drugs to market, and, even after the drugs are approved for common use, the potential of serious side effects for consumers. However, significant investments in technology development and research have resulted in transformative breakthroughs in alternative methods, enabling us to leave most animal testing behind.
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