The
@FDA CBER Director of Vaccines Review and Research, David Kaslow, has refused to multiple requests from ACIP to provide basic information re the testing that was done to detect potential DNA residuals in the mRNA COVID-19 vaccines!
According to him the FDA is not obliged to share with CDC, ACIP or the public how these products were tested for a known potential contaminant!
This is radical lack of transparency, that sabotages what
@SecKennedy attempts to establish!
It will be impossible to restore trust in public health and regulatory agencies with people with David Kaslow’s approach in charge…
🚨 THIS JUST TOOK A VERY SERIOUS TURN
First, I asked for Moderna’s underlying residual-DNA testing/validation records. I was VERY specific. I was told Moderna’s confidential information couldn’t be released.
So I changed the question.
Fine. Don’t give me Moderna’s records. Give me FDA’s own records showing FDA reviewed, evaluated and validated Moderna’s testing…including whether the KanR test actually represented the TOTAL residual plasmid DNA left behind.
If you have read Moderna’s Pre-Covid patents, been following Kevin McKernan and friends work, and Dr. Malones direct questioning at ACIP then you know why.
FDA searched. Today they replied:
“They found NONE responsive to that request.”
In plain English: I asked for the receipts showing the regulators checked Moderna’s homework. FDA couldn’t find any receipts.
And considering this testing was used to determine how much residual DNA remained in an injectable product given to millions of people?
WHERE. IS. THE. VALIDATION⁉️
Show us who checked Moderna’s homework⚠️