Discussion about this post

User's avatar
Dr Mike Yeadon's avatar

Steve,

I’m ex-pharma & I’m working with two others with experience of pharma manufacturing.

The reason was, my own non-manufacturing experience working with those who’s job it was to test & validate all the steps in making complex products told me this must be fraud.

It’s confirmed.

It’s literally impossible for the vaccines to have been manufactured to anything close to usual requirements.

We’ve seen regulatory exchanges with one of the pharma companies. In November 2020, the EMA assessors had SEVEN major objections. Usually, if there is one after a final regulatory filing, heads roll back at base.

Five weeks later, they got EUA.

Total fraud.

One expert has signed an affidavit stating in his opinion, these products don’t meet any of the usual requirements. It usually takes months not weeks to validate each step of a complex manufacture & you can’t move to the next step in a series.

Expand full comment
Dr Mike Yeadon's avatar

It’s criminal negligence to distribute a product of such variable character that you cannot assure the safety & efficacy.

Note the materials used in clinical trials used a totally different process than the billions of doses in the commercial product.

If the regulator waived the requirements they have committed crimes, because we’re all impliedly relying on the clinical trial data.

Expand full comment
506 more comments...

No posts