They no longer care because product safety, potency, integrity, strength, purity, and quality went out the window upon being granted Emergency Use Authorization. In the Pharma Quality Sphere, a single incident of a shipment of a batch being delivered outside of required/agreed-upon temp storage triggers a deviation and would be at least a moderate severity. There would be a risk assessment and probably subsequent destruction of said shipment.
As far as the “virus” vs “mutant” efficacy…
Well to this day, no one has been able to isolate a purified virus sample while thr CDC and WHO refuse to procure live samples. Combine that with the mRNA COVID patents appearing before the supposed virus was identified, and that tells you the vaxxes were never about the virus.
Combine that also with the negative efficacy with regard to patient outcomes, and it’s even more obvious and sinister.
They no longer care because product safety, potency, integrity, strength, purity, and quality went out the window upon being granted Emergency Use Authorization. In the Pharma Quality Sphere, a single incident of a shipment of a batch being delivered outside of required/agreed-upon temp storage triggers a deviation and would be at least a moderate severity. There would be a risk assessment and probably subsequent destruction of said shipment.
As far as the “virus” vs “mutant” efficacy…
Well to this day, no one has been able to isolate a purified virus sample while thr CDC and WHO refuse to procure live samples. Combine that with the mRNA COVID patents appearing before the supposed virus was identified, and that tells you the vaxxes were never about the virus.
Combine that also with the negative efficacy with regard to patient outcomes, and it’s even more obvious and sinister.