45-page version of the core US statutory history and legal implications.
Yesterday I participated in a call to orient an attorney new to the material. I was asked to put together a memo about US federal law on bioweapons reclassified as public health measures, 1969 to present.
To help them get up to speed as quickly as possible, I was also asked to provide a short synopsis at the top of the memo.
NUTSHELL: US Government since 1969 has incrementally transferred/hidden the joint DOD+HHS Chemical and Biological Warfare Program (50 USC 32) in the Public Health Service Act (42 USC 201) and Food Drug and Cosmetics Act (21 USC 9), such that federally-funded, federally-directed public health programs and products are actually bioterrorism programs and biological and chemical weapon attacks.
The government's purpose is to commit mass murder/depopulate the world, without public knowledge and without legal consequence, and enslave survivors for wealth and power centralization through digitized 'vaccine' passports and digital currencies, without public knowledge and without public resistance.
21 USC 360bbb-3, Authorization for medical products for use in emergencies, is one of the key pseudo-laws enabling the bioweapon attacks under the Covid-19 national emergency pretext.
21 USC 360bbb-3(k) is one of the key provisions:
(k) If a product is the subject of an authorization under this section, the use of such product within the scope of the authorization shall not be considered to constitute a clinical investigation for purposes of section 355(i), 360b(j), or 360j(g) of this title or any other provision of this chapter or section 351 of the Public Health Service Act [42 U.S.C. 262].
There is widespread public perception that Covid-19 information campaigns, masks, diagnostic tests, treatments and injectables are components in a public health program using experimental but regulated, ‘safe and effective’ medical products for the purpose of saving lives during a public health emergency.
They are not.
Covid-19 information campaigns, Emergency Use Authorized masks, EUA diagnostic tests, EUA treatments and EUA injectables are components of a mass murder operation using fear-mongering, fraud, propaganda, censorship and unidentified biological and chemical weapons.
Popular misunderstanding is deliberately and forcefully maintained by the political power brokers running the operation.
Two observable facts have helped some people see through the fog of this war, and continue to help more people see through it all the time:
FDA and other governments’ drug regulatory agencies have not withdrawn authorizations or approvals of the drugs, devices and protocols yet, despite millions of injuries and deaths experienced by recipients of the products during the initial deployment phase (January to November 2020, including the fraudulent clinical trials for the injections) and since the general deployment of the injections that began in December 2020. If the products were intended for medicinal, healing or protective purposes, and were subject to regulation governing research and development, production and use of medical drugs and devices, FDA and its counterparts in other countries would have stopped the programs as soon as the injuries and deaths became apparent. Instead, they have refused to even answer the question: “What is the stopping condition?”
Independent third-party verification of vial contents is prohibited under the terms of the DOD-mediated contracts between purchasing governments and manufacturing corporations. In typical drug regulation frameworks, according to Sasha Latypova, independent researchers can and do purchase products from manufacturers to verify that contents match labels and corroborate or disprove claims about safety and efficacy.
The fog has cleared somewhat, for many people.
We now know that there is no stopping condition, because use of the products “shall not be considered to constitute a clinical investigation.” If there is no regulated investigation, then there is no stopping role for a regulatory agency to perform, and the products are not medicinal drugs or devices: they are weapons.
We’re at a stage of trying to figure out non-regulatory ways that the mass murder can be stopped. We’re on the hunt for other, non-regulatory stopping conditions.
Lots and lots of people remain ignorant that the public information campaigns and products are weapons, and continue routinely following government recommendations, seeking out and using the products, ‘boosting,’ and dying from them. Eventually, the world population declines to the level the criminals find acceptable, and the cull phase will be done.
Or, lots more people figure out that the lies are lies, and the products are weapons, refuse to listen to any government recommendations, and refuse to seek out and use the products. Eventually, the criminals stop promoting the products and try to pretend the whole war never happened.
Or, lots more people figure out that the lies are lies and the products are weapons. Shortly after that market signal, the embedded administrative-state criminals escalate the war, deploying armed personnel to apprehend, detain and force-inject. The war stops being biomedical and covert, and becomes overt and bloody.
Or, a few people in key positions — federal and state legislators and judges — figure out that the lies are lies and the products are weapons, realize that a tipping point proportion of the People also understand it and find the courage to fight.
These key legislators and judges arrange for personal security to protect themselves and their families from assassination; terminate all emergency declarations; repeal all the enabling statutes and regulations; identify, isolate and remove the embedded criminals from government offices; and bring them to trial for their crimes.
Or, a few people in key positions figure out that the lies are lies and the products are weapons, but lack sufficient courage to get in the fight, and the biowar of attrition grinds on.