The FDA is involved in every aspect of the NIH, CDC, grants, PCR testing, data harvesting, collaborating with the Chinese for clinical reviews of drugs and compounds Pfizer is using in the nanoparticle of Comirnaty that are made in China, associating themselves with the DNAnexus platform partner, WuXi AppTec, and giving their inspection seal of approval to bioanalytical genomic labs in China. Wuxi AppTec has infiltrated large cities in the United States and is headquartered in Shanghai, China.
https://www.asianscientist.com/2014/10/tech/wuxi-offer-foundations-genomic-profiling-china/
Recently, the FDA approved the Foundation One test kit to scan for genetic markers in 324 genes for tumors and cancer to see if they qualify to receive entrectinib, made by Genentech. As in prior articles, Craig Venter, NIH Scientist of the Human Genome Project, formed the company and had patents with Pfizer, Roche, and various Pharmaceutical Companies to cure HIV and anthrax with CCR5 proteins that Pfizer is now using, in part to some degree, for covid therapeutics. The test kit can be found here on an NIH website for ordering. Roche, however, is the supplier of the test kit to International Health Professionals.
I might add that within 15 minutes of opening the https://www.ncbi.nlm.nih.gov/gtr/tests/527976/ web page linking to the NIH Genetic Testing Registry site, it was removed from the Brave search engine results completely. There was no trace of it in results or by going back to the initial search results after opening another selection after first finding it. But I had bookmarked it, so you may easily find it.
Now, before you start thinking of how good it is for them to cure cancer, there is something you should know. They’re hiding everything they’re doing within the scope of AIDS and cancer. They’re building the most elaborate, massive, genomic database you can even imagine that is fed by all of these sources including Stanford’s ENCODE, Microsoft and the St. Jude Cloud, Amazon, and Google’s Alphabet, and WuXi NextCODE. This massive database extends to the Word Health Organization’s WHONET and GLASS, also functioning on NIH funds of tracking multi-resistant staphylococcus aureus. China’s genomic sequencing efforts account for 20% of the global sequencing capacity.
China represents the largest market in the world for next-generation sequencing.
Next Generation sequencing is the catch-all hook phrase that is being used to promote some new thing that is out of the FDA’s scope of practice to be doing. As evidenced by the documentation of the overreach of the authority of the FDA, in regard to the complaint of potential public harm and suppression of future scientific advances and therapeutics, that was announced by Centers for Medicare and Medicaid Services April 12, 2018, found in FDA: Fostering Death to America Part 1.
No one knows where the positive covid test samples went for evaluation, but you can bet your sweet butt that those results are being genetically decoded, mined, and harvested, and going to China. The Human Genome Project has large gaps that artificial intelligence software got exceedingly wrong and became problematic due to it’s predictive failure, which they’re still trying to correct. In fact, this certain chromosome 8, which NIH Blast claims to contain the covid sequence, just happens to be the one they are having so much trouble with correcting and completing.
Another reason that they are trying to harvest everyone’s DNA on the planet is because they want your genome on your smartphone. Beyond that, WuXi AppTech wants to cross match every human’s plasma to be tailor made to every person, in every Continent, and every Country on the globe. How much do you think one bag of plasma in the hospital costs? I’ll accept any and all answers for a guess, but the truth is, that one bag of plasma as an in-patient in the hospital is $20,000/bag. If you're an in-patient, and one bag seems to show an improvement in your condition, you might get 2 bags. That’s $40,000 for some antibodies that were bought after plasma donation from someone else for, let’s say, $200, that may or may not help you. What Wuxi wants to do is make a synthetic version for everyone. Quite commendable and ambitious. I don’t know what they’re planning on making it from, but it’s my guess it has to do with abortions and cloning. Just as has been seen with Regeneron and the lipid nanoparticle from a metabolite of an aging mouse brain, it will probably integrate mice and hamster metabolites and foster surrogacy to grow things on or in them, to be drawn back out and inserted into you. As was the case with Regeneron, it was grown in hamster ovary cell culture.
Did you catch that? Animal/human derived raw materials need extensive safety testing. Are they talking about milk, meat, breast milk, or something else? Regarding the viral vector release testing, that is pretty scary to me, because I know that they are using viral vectored viruses to treat illnesses that have nothing to do with what they are treating.
For example, monkeypox (vaccinia virus) is being used as a vectored vaccine for AIDS and influenza. It’s been deemed to be a good candidate and is safe to use on humans.
An adenovirus from a monkey that is patented by Francis Collins and being used in the covid vaccines is causing hepatitis. And on, and on. For decades, since the 1950’s, scientists have been using a virus to try to cure a disease that has nothing to do with it. As was the case with the murine leukemia virus from an African monkey that the Merck scientist admitted to using in an effort to cure polio but ended up causing cancer.
I’m sure we’ll hear nothing out of Francis Collins and his Chinese counterpart who shares in the patent of the cystic fibrosis gene that is being used with his adenovirus patent for all of the pain and suffering of small children and adults due to his greed and neglect.
The Emergency Use Authorization for research and therapeutics is being used in perpetuity to continue the mass charade.
WuXi AppTech and DNAnexus see themselves as a promulgation of the FDA working in tandem to achieve corresponding goals.
DNAnexus received funding from Regeneron, one of the only companies a therapeutic was made available from, and received FDA approval.
I just hope we have the foresight to look back on this time in our lives and never let something like this happen ever again. We can’t see the future, but we certainly can look at the past and take a lesson of what not to do the next time, and I hope we can all adhere to it from what we’ve learned: We can’t trust the FDA.
*This is a working draft, your patience to allow me to expand and add further research documentation to it to further support and confirm the findings are appreciated. They will be added and revised as time allows. Thank you.