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Costa Rica Supreme Court Wins
Costa Rica’s Constitutional Court found the Immunization Coordinator in default for ignoring a judicial order to produce WHO safety data—effectively refusing the court’s mandate. In a stunning twist, two national agencies admitted these COVID products are not vaccines but experimental biologics imported without proper legal authority. This landmark default voids WHO’s EUL in Costa Rica and sets a powerful global precedent for demanding emergency listings be withdrawn.
Default Ruling – May 6, 2025US Citizen Petition & VRBPAC
On May 22, 2025, we demanded FDA classify mRNA/viral vector products as gene therapy (21 C.F.R. § 600.3(h)(5)) and trigger a clinical hold under 21 C.F.R. § 312.42. Our VRBPAC testimony exposed critical safety and consent failures.
Legal Rationale
- Ultra Vires: WHO EUL lacks authority under domestic law. Products exceed legal mandate.
- Gene Therapy: Mechanism modifies human DNA—squarely within FDA’s gene therapy framework.
- Clinical Hold: Code §312.42 empowers FDA to pause trials when safety is uncertain. Risks remain hidden.
- Delist WHO EUL: Once FDA reclassifies or withdraws, WHO listing is void—US authority drives global status.
- Monthly Impact: Ongoing legal costs demand sustainable support—join our monthly donors.
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