Mark Lanman

The National Childhood Vaccine Injury Act (NCVIA) of 1986 (42 U.S.C. §§ 300aa-1 to 300aa-34) was signed into law by United States President Ronald Reagan as part of a larger health bill on November 14, 1986. NCVIA’s purpose was to eliminate the potential financial liability of vaccine manufacturers due to vaccine injury claims^[1] in order to ensure a stable market supply of vaccines, and to provide cost-effective arbitration for vaccine injury claims.^[2] Under the NCVIA, the National Vaccine Injury Compensation Program (NVICP) was created to provide a federal no-fault system for compensating vaccine-related injuries or death by establishing a claim procedure involving the United States Court of Federal Claims and special masters.^[1]^[3]

In other words, this Act granted the vaccine industry blanket immunity from ALL product liability for injury or death resulting from the use of their products. In exchange, this Act required the vaccine manufacturers to submit to the Dept. of Health and Human Services (“HHS”) reports periodically pursuant to §300aa-27 the Act.

1. Section 300aa–27. Mandate for safer childhood vaccines

(a)General ruleIn the administration of this part and other pertinent laws under the jurisdiction of the Secretary, the Secretary shall—

(1)promote the development of childhood vaccines that result in fewer and less serious adverse reactions than those vaccines on the market on December 22, 1987, and promote the refinement of such vaccines, and

(2)make or assure improvements in, and otherwise use the authorities of the Secretary with respect to, the licensing, manufacturing, processing, testing, labeling, warning, use instructions, distribution, storage, administration, field surveillance, adverse reaction reporting, and recall of reactogenic lots or batches, of vaccines, and research on vaccines, in order to reduce the risks of adverse reactions to vaccines.

(c)Report

Within 2 years after December 22, 1987, and periodically thereafter, the Secretary shall prepare and transmit to the Committee on Energy and Commerce of the House of Representatives and the Committee on Labor and Human Resources of the Senate a report describing the actions taken pursuant to subsection (a) during the preceding 2-year period.

From the court documents:

In August 27, 2017 the INFORMED CONSENT ACTION NETWORK (“ICAN”) submitted a Freedom of Information Request to the Secretary of the Dept. of Health and Human Services asking for transmit to the Committee on Energy and Commerce of the House of Representatives and the Committee on Labor and Human Resources of the Senate a report describing the actions taken pursuant to subsection (a) during the preceding 2-year period.

In June 27, 2018, HHS sent ICAN the following response to their request.

The [Department]’s searches for records did not locate any records responsive to your request. The Department of Health and Human Services (HHS) Immediate Office of the Secretary (IOS) conducted a thorough search of its document tracking systems. The Department also conducted a comprehensive review of all relevant indexes of HHS Secretarial Correspondence records maintained at Federal Records Centers that remain in the custody of HHS. These searches did not locate records responsive to your request, or indications that records responsive to your request and in custody of HHS are located at Federal Records Centers.

BOOM!BOOM!BOOM!

LOS ANGELES, Sept. 14, 2018 /PRNewswire/ — The U.S. Department of Health and Human Services (HHS) has admitted that, in direct violation of Federal law, it failed to provide a single vaccine safety report to Congress for thirty years, according to Informed Consent Action Network (ICAN).
Congress therefore charged the Secretary of HHS with the explicit responsibility to assure vaccine safety. Biannual reports of HHS’s progress in improving vaccine safety were to be submitted to Congress. Yet, as ICAN has now proven, these reports were never created.[1]

This is the smoking gun. This is one of many rebuttals to any “MANDATORY” vaccine orders. There is NO EVIDENCE any of the scheduled vaccines are SAFE and EFFICACIOUS, nor will there be because the industry is not compelled to test their products, they have immunity from any liability. In fact, its a matter of record a leading manufacturer of the alleged COVID-19 VACCINE skipped crucial animal trials to “FAST TRACK” its development, ignoring toxicology analysis. [2]

When the claim is made “vaccines are safe, and effective” – ask for proof. This court case forced the Secretary of Health and Human Services to admit no reports have been created. In other words, the medical establishment has not provided ANY reports since the Act was signed into law, that show proof vaccines are safe and efficacious.

Court Case: https://olis.leg.state.or.us/liz/2019R1/Downloads/CommitteeMeetingDocument/168629

Response by Robert Kennedy Jr., to this court case. https://www.prnewswire.com/news-releases/ican-vs-hhs-key-legal-win-recasts-vaccine-debate-300712629.html

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