MHRA and regulatory

Zeal to Push COVID-19 Immunization Program Risked More Lives

Dr. Helene Banoun Elucidates the History of Misguided Use of Genetic Code for Vaccination

Emergency Authorization Granted without Emergency or Human Data

The MHRA, the watchdog covering up the truth about vaccine deaths and injuries

Why isn't the MHRA investigating vaccine deaths?

It would appear to be a happy and satisfying relationship. "Our priorities are aligned," says one document. There have been "notable successes" says another, citing "another example" of where the two sides "cooperated well". In business partners, this would seem to indicate a harmony of views. The documents obtained by the Guardian, however, relate to meetings between the drug industry and the watchdog body set up by government to police it.

More reckless sign-offs from the regulators

Regulatory capture is a theory that regulatory agencies may be dominated by the interests they regulate and not by the public interest.

In light of the EU’s Covid-19 response, it is clear that the actual emphasis is likely to be placed on mRNA.

The “Future Framework” would take the “flu strain selection process” that fails yearly and apply it to future (reformulated) Covid-19 shots.

#1 on AMAZON, and a NEW YORK TIMES, WALL STREET JOURNAL…

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Billionaire Warren Buffett says leaders aren't always making rational decisions, and companies too often copy one another without critical thinking. Here's why the concept he calls "institutional imperative" is important.

...and there's an awful lot in the can!

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It should have been...

Hedley Rees is a drug development expert and author. Rees is the Managing Consultant at PharmaFlowLimited, a UK-based consultancy specializing in supply chain management within the pharmaceutical and

The experts warn that cardinal symptoms of cerebral venous sinus thrombosis (CVST) dominate the list of adverse reactions to COVID-19 vaccines.

The methodology of a UK report concluding that COVID-19 vaccines are unsafe for use in humans was applied to adverse event data in the USA.

A Freedom of Information request to the Australian drugs regulator that approved the Pfizer vaccine confirms that they have never seen the study data.

Read Doctors for Covid Ethics' letters to and from the European Medicines Agency (EMA). In those letters we seek evidence that foreseeable vaccine dangers were ruled out prior to human use, and call for a halt to COVID-19 vaccines on urgent safety grounds. Our first letter of warning was issued prior to clot-related vaccine suspensions around the world. Open Letter The Eternal Dangers of mRNA

Pfizer is using children as legal human shields to get full authorization.

Company claims it is manufacturing Comirnaty product with new formula.

Buried in the fine print of Monday’s approval by the U.S. Food and Drug Administration of the Pfizer Comirnaty COVID vaccine are two critical facts that affect whether the vaccine can be mandated, and whether Pfizer can be held liable for injuries.