Brilliant article by Katherine Watt. Please sponsor her work as I do.
Regulation or licensing of biological product and vaccine manufacturing in the United States, by the Food and Drug Administration and its precursors, establishes and applies alternative, surrogate, proxy, indirect, uncontrolled, correlative, probability-based standards to manufacturing methods and product quality assurance methods.Because the standards are correlative, and therefore not standards at all, the procedures presented to the public as regulation have instead been a simulation of regulation, a suggestion-to-the-mind of observers, without substance or materiality.Regulatory simulation of biological product manufacturing has been going on continuously since the initial construction of the legal frameworks for biological products in 1902 with Congressional passage of the Virus-Toxin law, through the present.The basic reason for the simulation is that the simulators have want the public to believe — contrary to the truth — that vaccines are a class of products that can be stabilized and standardized and, in stable, standardized, identifiable and identified forms, can be demonstrated to have stable properties or attributes such as purity, therapeutic effectiveness and strength.These properties are denoted using many different terms within legal instruments. Some of the other terms are sterility, safety, efficacy, specific results, potency, dosage, contaminated, adulterated, adventitious agents, bioburden, extraneous proteinsBecause the contents of vaccine bottles are propagated by living organisms, vaccines are processes, and not products. And because they are non-self organic matter, injected into the blood of a recipient organism, they can also be understood as injectable pesticides. They offer a much more concentrated, effective delivery mechanism than aerial and surface spraying.As living organisms or dynamic processes encased in steel or glass, vaccines cannot be fully identified, defined, characterized, stabilized or standardized, and thus cannot be demonstrated to have stable properties or attributes such as purity, effectiveness and strength.Regulation and standardization in a substantive, material form is practically and theoretically impossible.Over the past eight decades, those who use vaccines to poison babies, children and adults under the guise of therapeutic benevolence have made changes to the wording of biological product and communicable disease control law. In most cases, these wording changes have been driven by an interest in obscuring or delaying emergence of evidence from advancements in analytical techniques and equipment, which would expose the intentional harmfulness of vaccination to public view, and to compensate for growth in public scientific literacy.Why have legislators, financial officers, military officers, public health officers, scientists, vaccine manufacturers, doctors and lawyers wanted people to believe the lies that a non-standardizable process is a standardized product and that harmful products are beneficial products?We believe the evidence supports the conclusion that these government officials and professionals seek to induce false trust by suggesting feasible and rigorous quality control oversight where none occurs, and to ensure product safety and therapeutic benefit, where neither are possible, to induce compliance with vaccination campaigns.They want people to take vaccines voluntarily, repeatedly and without resistance, and to vaccinate their children, so that more people will get sick, be sicker, and die earlier, without the poisoning crimes being traceable to the killers, and within a legal system incapable of stopping, prosecuting and punishing the criminal acts.We believe the evidence supports the conclusion that biological product regulation is a web of interwoven simulations, and that the evidence demonstrates how and by whom these simulations are performed.Some of the performers — vaccinating doctors, nurses and pharmacists who have trusted the information provided to them during training and the teachers who provided that information — have believed they are performing good acts with true therapeutic, disease-prevention effects. They believed error to be truth, but they believed it sincerely and with good will, out of ignorance and not malice.For some of the performers who know the truth about epidemiology, pathology, virology and vaccines, the motivation is greed and the goal is money: patient visits, drug sales, campaign contributions, bribes, getting people on the public dole as disabled, and then off the public dole as dead.For others who know the truth, and who organize the work of doctors, nurses, pharmacists, manufacturers, legislators, judges and civil administrators, it’s about dominance, control, and exploitation.It’s war, disguised.It’s about destruction of life and productive capacity.It’s about orchestration of scarcity.It’s about keeping people sick, weak, disordered, indebted, confused, depressed, anxious, dependent, infertile,