It is yet another example of bureaucracy at it's finest.
COVID-19 mRNA vaccines are, by mode and action, gene therapy products.
U.S. and European regulatory agencies did not classify them as such. These products were regulated as ordinary vaccines against infectious diseases instead of being subjected to the more stringent regulation of gene therapy products.
You may ask, "now why would they do such a thing? N.W.O. ? Eating ze bugz ? Conspiracy theories ?"
I personaly don't buy it. The research and development, regulations and manufacturing processes are obviously both time and cost consuming.
Labeling a product under a different category is an excellent way bypass the rules, save time and money.
If these vials of piss were indeed labeled as gene therapy products, the ŕequired preliminary tests would have included :
-Genotoxicity.
-Genome integration.
-Germ-line transmission.
-Insertional mutagenesis.
-Tumorigenicity.
-Embryo/fetal and perinatal toxicity.
-Long-term expression.
-Repeated toxicity.
-Excretion in the environment, such as shedding through seminal fluid or breast milk."
This would have cost Pfizer and Moderna $$$$$$$ and instantly obliterated their chances to receive ANY form of approval for their candidate products.
