Aura Asset Intelligence
While the focus is on faulty RT-PCR testing, growing cases based on the tests amplified by more panic from “official sources” who either don’t understand or seem to care what the repercussions have caused thus far. The mantra continues to be get vaccinated to overcome SARS-CoV2. An invention patented by the Perbright Institute and CDC in which the CDC admitted the so-called “virus” was a computer generated simulation and the creator of the RT-PCR test Kary Mullis said:
“Anyone can test positive for practically anything with a PCR test— Kary Mullis
If that were not enough, the “vaccine” fails to meet the following five requirements to be considered a vaccine and is by definition a medical “experiment” and trial for gene therapy: In fact the drug companies and FDA are quite open about calling it what it is: a “post marketing surveillance study.” Without the Emergency Use Authorization (EUA) it would be impossible for the pharmaceutical industry to distribute an experimental product en mass especially when there is other means available to treat covid namely ivermectin, hydroxychoriquine, zinc, vitamin C and D as well as many other non-evasive remedies rendering the need to develop a “vaccine” according to the FDA’s own guidelines under 21 USC 355: New drugs TITLE 21–FOOD AND DRUGS CHAPTER I totally unnecessary and less effective than existing drugs..
§355. New drugs21 USC 355: New drugs
(a) Necessity of effective approval of application
No person shall introduce or deliver for introduction into interstate commerce any new drug, unless an approval of an application filed pursuant to subsection (b) or (j) is effective with respect to such drug.
Section 505 of the Act describes three types of new drug applications: (1) an application that contains full reports of investigations of safety and effectiveness (section 505(b)(1)); (2) an application that contains full reports of investigations of safety and effectiveness but where at least some of the information required for approval comes from studies not conducted by or for the applicant and for which the applicant has not obtained a right of reference (section 505(b)(2)); and (3) an application that contains information to show that the proposed product is identical in active ingredient, dosage form, strength, route of administration, labeling, quality, performance characteristics, and intended use, among other things, to a previously approved product (section 505(j)). Note that a supplement to an application is a new drug application.
Because the Food and Drug Administration (FDA) is an agency established by federal law, there are clearly defined pathways along which a drug can be approved. A drug development program is a process that requires an understanding of the content and purposes of sections 505(b)(1) and 505(b)(2) of the Federal Food, Drug, and Cosmetics (FD&C) Act.
A “Listed drug” is a new drug product that has been approved under section 505 of the Federal Food, Drug, and Cosmetic Act for safety and effectiveness or under section 505(j) of the Federal Food, Drug, and Cosmetic Act, which has not been withdrawn or suspended under section 505(e)(1) through (5) or section 505(j)(6) of the Federal Food, Drug, and Cosmetic Act, and which has not been withdrawn from sale for what FDA has determined are reasons of safety or effectiveness. Listed drug status is evidenced by the drug product’s identification in the current edition of FDA’s Approved Drug Products With Therapeutic Equivalence Evaluations (the list) as an approved drug. A drug product is deemed to be a listed drug on the date of approval for the NDA or ANDA for that drug product.
Upon closer examination by independent researchers and laboratories, several toxic substances have been found in masks, test-kits and all the inoculations.Graphene Oxide a highly conductive toxic material that is used for self assembly for what is called TESLAPHORESIS With an increasing number of people becoming aware of graphene oxide being identified in covid vaccines, a company called INBRAIN Neuroelectronics demonstrates that graphene-based “neuromodulation” technology using AI-powered neuroelectronics is very real:.
[GRAPHENE IN VACCINES] NANOTUBES ASSEMBLE! RICE INTRODUCES TESLAPHORESIS (WORKING EXAMPLE).
Title 21- 321 h Describes what a “Device” is
Title 21 Part 314 “Applications For FDA Approval To Market A New Drug” purpose is to establish an efficient and thorough drug review process in order to: (a) Facilitate the approval of drugs shown to be safe and effective; and (b) ensure the disapproval of drugs not shown to be safe and effective. These regulations are also intended to establish an effective system for FDA’s surveillance of marketed drugs. These regulations shall be construed in light of these objectives.
With this new technology, it’s impossible to predict what will happen in the future. Computer modeling reproduces a predetermined outcome that rarely if ever mimics natures unpredictably complex balance to prove the product’s safety and efficacy for the indication being sought. And what is it the manufacturers claim their products do?
What is “Safe and Effective?”
Safe and effective is defined in Federal Food Drug and Cosmetic Act, USC section 505(b)(1)
SAFE Acronyn for surgery, antibiotics, facial cleanliness and environmental change. This complex of measures is a strategy for the control of TRACOMA and has been shown to be effective in endemic areas.
SAFE Cardiology A clinical trial–Safety After Fifty Evaluation – a set of this many persons or things.
EFFECTIVE actually in force. Producing a strong impression or response; striking:
Vaccine Makers Claim COVID Shots Are ‘95% Effective’ — But What Does That Mean?
Are Pfizer and Moderna misleading the public about the efficacy of their COVID vaccines by withholding the fact that there’s another way to parse their data — one that has more real-world significance?
When one does the math, the Pfizer clinical trial numbers showed: “The risk reduction in absolute terms [was] only 0.7%, from an already very low risk of 0.74% [in the placebo group] to a minimal risk of 0.04% [in the vaccine group].” (Dividing 0.7 — the difference between the two groups — by 0.74 is the mathematical calculation that produced the touted “95% effective” number).
Source: The Defender
DR. NORTHRUP DISCUSSES “WORST CASE SCENARIO” WITH NEW COVID VACCINE DANGERS
- Bill Gates, Vaccinations, Microchips, And Patent 060606
- Cryptocurrency system using body activity data
- BIOMETRIC HEALTH PASSPORTS AND THE PANOPTICON
- COVID MRNA VACCINE NOT A VACCINE
NEWS & VIEWS FROM THE NEFARIUM | DR. JOSEPH P. FERRELL
Researchers in the United States have developed a new method for controlling the brain circuits associated with complex animal behaviours, using genetic engineering to create a magnetised protein that activates specific groups of nerve cells from a distance.Wheeler, M. A., et al. (2016). Genetically targeted magnetic control of the nervous system
Pentagon Creating ‘Neural Interface,’ Linking Humans to Machines
By Eric Mack
The Defense Advanced Research Projects Agency (DARPA) is reportedly working on “neural interface” for humans to connect to military systems with their mind – “technology would let people control, feel, and interact with a remote machine as though it were a part of their own body.”
“From the first time a human carved a rock into a blade or formed a spear, humans have been creating tools to help them interact with the world around them,” DARPA’s Biological Technologies Office program manager. Al Emondi told Defense One. “The tools we use have grown more sophisticated over time . . . but these still require some form of physical control interface — touch, motion or voice. What neural interfaces promise is a richer, more powerful, and more natural experience in which our brains effectively become the tool.” Seeds of the technology have already been put to work with DARPA’s Revolutionizing Prosthetics program where disabled veterans can control a prosthetic limb “using an electrode implanted in their brain,” according to the report.
Altruism is not DARPA’s strong suit. Their objectives are for military applications. Prosthetics serve as a lost leader and PR tool justifying further R&D, funding and continued growth of their ecosystem.
FACEBOOK META – IS VIRTUAL REALITY A SOUL TRAP?
DR THOMAS COWAN – 5G AND CORONAVIRUS CONNECTION
TRANSHUMANISM AND YOU
- The New Nuremberg Trials 2021: Update From Dr. Reiner Fuellmich
- COVID mRNA “vaccine” is not a vaccine
- World Economic Forum Releases Guide on How to Coerce and Manipulate Public into Getting the Covid-19 Vaccine
- Government document instructs vaccine “strike force” teams how to clear buildings, violate trespass laws and flag anti-vaxxers for forced quarantines
- Transhumanism & Eugenics: Scientists Reveal Jeffrey Epstein’s Plan To Create Breakaway Civilization
- “Scariest Thing You’ll Read All Day”: Report Sounds Alarm Over Brain-Reading Technology and Neurocapitalism
- The Invisible Rainbow
- BRAINWAVES CONVERTED TO SPEECH
- GRAPHENE IN JABS!!! (YOU KNOW IT!) STILL YET MORE INDICATIVE CONFIRMATIONS
AHEAD OF THE CURVE
Hellooooo…. There IS No ‘Virus’
“We need to increase public understanding of the need for medical counter measures such as a pan corona vaccine. A key driver is the media and the economics will follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond if they see profit at the end of the process”— Peter Daszak (Head of ECO Alliance)