SARS-CoV-2 injections should never have been frozen—find out why

This is so important in understanding how bad SARS-CoV-2 injections are

In January, I wrote this article, about a complaint I has sent to the European Medicines Agency:

FROZEN SARS-CoV-2 INJECTIONS BROKE THE LAW

Why didn't FDA/MHRA/EMA notice?

It begins:

“On December 21 2020, I wrote the following to the European Medicines Agency (EMA):

Subject of your enquiry: GMDP in relation to COVID-19 vaccines that are delivered to vaccination centres bypassing the wholesaler networks

”Dear EMA,

I am an experienced consultant in biopharmaceutical supply- chains. I wish to enquire how the inspectorate with assure GMDP [Good Manufacturing and Distribution Practice] and appropriate quality systems will be maintained with regard to patient safety for the frozen and ultra cold vaccines being assessed for emergency approval? It appears to me that these vaccines are being despatched from manufactures part-finished ie not in the final dosage form for patient administration and there represents a potential risk if untrained personnel, working outside the bounds of a quality system, are employed in ordering, processing and inventory management of the vaccines, also, what is the status in regard to the falsified medicines directive, 2011, in regard to traceability in the case of a serious adverse event of other reason for product recall.

Your, Hedley Rees””

The reply, two months later, was a series of website links that were meaningless in relation to the complaint. We have since come to expect that from Regulatory Authorities.

Part 2 explained more

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