Liability for coercing participation in a medical experiment, and any injury from it, may be incalculable. Children’s Health Defense urges U.S. employers, universities and other institutions to respect and uphold the rights of individuals to refuse EUA tests.

1227 North Peachtree Parkway, Suite 202. Peachtree City, GA 30269
www.childrenshealthdefense.org

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(I) that the Secretary has authorized the emergency use of the product;
(II) of the significant known and potential benefits and risks of such use, and
of the extent to which such benefits and risks are unknown; and
(III) of the option to accept or refuse administration of the product, of the
consequences, if any, of refusing administration of the product, and of the
alternatives to the product that are available and of their benefits and risks.

EUA products are by definition experimental and thus require the right to refuse.
Under the Nuremberg Code, the foundation of ethical medicine, no one may be
coerced to participate in a medical experiment. Consent of the individual is
“absolutely essential.” A federal court held that even the U.S. military could not
mandate EUA vaccines to soldiers. Doe#1 v. Rumsfeld, 297 F.Supp.2d 119 (2003).
The Food and Drug Administration (FDA) has issued Emergency Use
Authorizations for over 200 diff

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maybe this will help. Also ask for federal law where it is mandatory to give you this test. You want specific law. The Children's health Defense is an excellent website to get info.
NOTICE FOR EMPLOYERS, UNIVERSITIES AND OTHER INSTITUTIONS
MANDATING COVID-19 TESTS

April 26, 2021

This serves as notice that the mandate for any individual to be tested against
COVID-19 for employment or participation at a university or other institution
violates federal law. All COVID-19 tests, whether polymerase chain reaction (PCR),
antigen tests or others, are authorized, not approved or licensed, by the federal
government; they are Emergency Use Authorization (EUA) only. They merely “may
be effective.” Federal law states:
Title 21 U.S.C. § 360bbb-3(e)(1)(A)(ii)(I-III) of the Federal Food, Drug, and Cosmetic
Act states:
individuals to whom the product is administered are informed—

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