Toxic Impurities In Covid Shots

Written by Phillip Altman on October 9, 2023. Posted in Current News

Poor quality control in manufacturing results in toxic DNA and endotoxin impurities in the COVID injections which explain the high incidence of serious adverse reactions and deaths linked to the shots

This is important…..very important. Many commentators, including myself, have previously referred to highly toxic DNA and endotoxin contamination in the COVID injections over many months.

Let me explain and summarise the situation for you.

GOOD MANUFACTURING PRACTICE (GMP) STANDARDS

A significant part of the thousands of pages of drug regulatory guidelines issued by both national and international organisations which govern the development of new pharmaceutical products are devoted to the chemical synthesis, purification, scale up manufacture and quality control of both the active ingredient and the final product formulation.

These guidelines can be found under the umbrella of generally accepted Codes of Good Manufacturing Practice (cGMP). There are other guidelines for the animal toxicity (safety) testing and still more voluminous guidelines for the design, management and reporting of clinical trials, data analysis etc.

As a regulatory affairs and clinical trial consultant to many pharmaceutical companies, it was my job to keep abreast of all the regulatory guidelines to ensure that any work I did for a client company complied with the latest national and international regulatory requirements.

To get a feeling for the scope and depth of some of these guidelines I refer my readers to the International Conference on Harmonisation (ICH) website (CLICK HERE) and for a sample of the specific Australian Therapeutic Goods Administration (TGA) GMP information (CLICK HERE).

The point I am trying to make is that it is clearly understood, in great detail, by all drug regulators and the pharmaceutical industry that certain minimum standards MUST be attained to ensure a reasonable level of safety for pharmaceuticals.

I have repeatedly stated that the development of the COVID so-called “vaccines” have neither complied with the acceptable GMP standards, animal testing standards or clinical trial standards to ensure an acceptable level of quality, safety and efficacy.

The reason being that the US Dept of Defense was in command and control of the development of the COVID injections and expedited their production and release to the public by cutting corners and sacrificing quality, safety and efficacy standards in the name of countering a perceived pandemic threat.

I refer my readers to my Substacks of Feb. 27 (CLICK HERE) and April 5 (CLICK HERE).

Just focusing on GMP issues, it has been widely reported for some time that toxic contamination of the COVID shots in the form of plasmid (circular) DNA and endotoxins posed a massive safety risk.

The plasmid DNA contamination has the potential to integrate into your own DNA and even carry over to future generations. See my previous Substacks of 2 June (CLICK HERE) and 8 Sept (CLICK HERE).

The endotoxin contamination described by Australian Dr. Geoff Pain (CLICK HERE) and (CLICK HERE) has been acknowledged by eminent researchers such as Dr. Kevin McKernan as being of particular importance and may account for hundreds of adverse event types reported in relation to the COVID injections including neurological and cardiovascular effects and some cases of sudden death following injection.

Dr. Pain was the first person I noticed to comment on what has become known as Process 2 manufacture of mRNA for the Pfizer shots. CLICK HERE to read his Substack of 29 January.

This is truly amazing……….It appears now that the mRNA manufacturing process used to make the mRNA for the Pfizer “vaccine” clinical trial was different to the mRNA manufacturing process used by Pfizer to produce commercial lots.

The clinical trial “vaccine” mRNA was manufactured using RT-PCR (real-time polymerase chain reaction) methods but the commercial batches used plasmid DNA and E coli bacteria fermentation (PROCESS 2).

This change in manufacture for commercial lots meant that toxic DNA and endotoxin contamination necessarily occurred as part of the manufacturing process and it was necessary to subsequently remove these toxic contaminants…….but were they sufficiently removed?

PROCESS 2

Israel was used as a test lab for a massive Pfizer vaccination campaign. Now an Israeli scientist speaks out about the danger of the use of PROCESS 2 to manufacture the Pfizer “vaccine”. CLICK HERE to view (43 min).

It is widely known that plasmid DNA and endotoxins are dangerous and there must be a specification which limits their presence in any final pharmaceutical product. Some regulatory agencies have raised this concern already but nothing seems to have been done about it.

Our TGA simply denies any danger posed by the DNA without providing any credible evidence to support such a claim and they are silent in relation to endotoxin contamination.

They are not doing their job and they must be held to account.

THE VOICE – YOU MUST WATCH THIS

Douglas Murray knocks it out of the park…….CLICK HERE to listen to 9 minutes of cogent analysis.

This is real “truth telling”.

See more here substack.com

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