In August 2015, during the Obama administration, the FDA became involved with Obama’s Precision Medicine Initiative. The avenue to harvest the DNA of Americans uses a precisionFDA platform owned by DNAnexus. Tests being performed in laboratories and Doctor visits screening for cancer and genetic specimen comparisons, are uploaded into the database.
Stanford University
The Stanford Data Coordination Center (DCC) Encode (Encyclopedia of DNA Elements) project, is a genomic data collecting Phase 3 project of the Human Genome Project and National Institutes of Health.
In June 2015, DNAnexus announced the collaboration of the Stanford DCC ENCODE project to be hosted on the DNAnexus platform.
During the Human Genome Project, as stated in a previous article, 6 Countries participated in the sharing of genomic data, and China was one of them. We shouldn’t be surprised how out of hand this has gotten, because from the very beginning there were disputes and Court filings over the ownership of the genomic sequences and proteins that were being discovered by NIH Scientists. Some of those disputes pertained to patents, methods of causing DNA to produce proteins, and predictive artificial intelligence software.
While in the employ of the NIH, the NIH would ultimately have the legal right to claim a 50% portion of the patent, and the remaining portion is shared with the Scientist in the employ of the NIH or grant funded Institution.
When covid came along, it was Stanford University who was commissioned by the CDC to provide an artificial intelligence model covid sequence.
The FDA and CDC are the Regulatory Authorities of the NIH grants. Institutions receiving grants comply with the governing Internal Review Board policies set by the NIH, CDC, and FDA.
It’s clear that Stanford was one of the Universities receiving funding from the NIH and Human Genome Project, but there are many Pharmaceutical Companies who participated in the Human Genome Project, including Pfizer, who received grants.
The former FDA Commissioner, Albert Bourla, and a host of conflicts of interests fill the rolls of FDA approved rosters. One of which was found in Dr. Fauci’s emails pertaining to Celularity.
Schering Plough, also a participant in hosting the Human Genome Project, is cited as being in collaboration with a patent Pfizer is using for Paxlovid using light vibration spectrum tuning technology.
Fisher Scientific (Thermo-Fisher) and Abbott Laboratories have a big part to play in this as well, because the FDA approved their covid products for PCR tests which yielded numerous false positives to the point of discontinuation. Thermo-Fisher and Abbott have a history of being reprimanded by the FDA for faulty products, yet they continue to let them pursue approval even when they know their track record manufactures faulty, harmful, and ineffective products. Thermo-Fisher PCR tests are made by WuXi-AppTech, which will be discussed in FDA: Fostering Death to America Part 2.
Abbott Laboratories is heavily invested in RFID chips. Their at-home covid tests gained so much negative attention they were taken off the market around the same time the FDA shut down their baby formula facilities. The heat from the faulty covid tests and RFID technology was replaced by a name of being notorious for baby formula. But, they didn’t do that right either.
Why is the FDA accepting clinical reviews for Comirnaty from Chinese Scientists located in Wuhan? This is not an accident. It’s a well planned, carefully detailed and documented genocide with a license to kill.
With a host of other Chinese sounding names, looking into it any further when one of them leads to Wuhan seems rather unproductive. I challenge anyone who has the patience to do so to research these names, and I may be able to tie some of them together with the research I’ve found on Paxlovid, NIH employed Human Genome Scientists of Extramural and Intramural Research from China, or with known associations of the National Medical Association.
The compounds Pfizer is using to make the nanoparticle of the vaccines and in the therapeutic, Paxlovid, are made in China.
DNAnexus is the platform that supports Rockefeller University Genome Ark and the Vertebrate Genomes Project. One of their Scientists of the BAT 1K project is in Wuhan, China. Rockefeller University is interested in using bats to prolong life and discover the secret to longevity by studying them.
The FDA was fundamental in procuring abortion organ and tissue samples from Planned Parenthood that were sent by Fed-Ex.
The FDA approved VeriChip. It’s very clear that the approval of this mechanism, the chip that is placed in tissue in the arm, and the pocket reader are intended to be used as a form of the patient’s verification of identity and ready access to patient medical record health data.
The FDA afforded Verichip with a class status that it wasn’t eligible for before 1976, but they seem to have moved it up the ladder and made an exception to graduate it to acceptability to enjoy the status that was beyond the intent of the former regulations.
An implantable radiofrequency transponder system is intended to enable access to secure patient identification and corresponding health information. This system may include a passive implanted transponder, inserter, and scanner. The implanted transponder is used only to store a unique electronic identification code which is read by the scanner. The identification code is used to access patient identity and corresponding health information stored in a database.
The FDA is making predictions as to how they plan to launch gene therapies in the coming years. They expect to release 10-20 cell and gene therapy products a year by 2025.
The FDA didn’t have the authority to authorize genetic testing and Next Generation Diagnostics. That authority was made clear in a document stating that given authority in such matters were given to and covered by Centers for Medicare and Medicaid Services, and deemed that what the FDA was doing was putting the public at risk and was potentially harmful to future discovery and innovation.