A shocking new report details numerous systematic ongoing failures at the Medicines and Healthcare Products Regulatory Agency (“MHRA”) which is responsible for the safety and efficacy of medicines in the UK.
On 19 April a detailed report into the failings of the UK medical regulator was published. The multi-disciplinary team of authors of the report, The Perseus Group, remain mostly anonymous, but both Nick Hunt, a retired civil servant who worked in weapons safety regulation, and Hedley Rees, who had a career in pharmaceutical manufacturing, have both been interviewed as authors of the report.
The Light has more on the story.
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MHRA failed the public over vaccine
As published in The Light, Issue 33
The Perseus Group report highlights how failures at the regulator resulted in the public being exposed to serious side effects such as myocarditis, blood clotting, neurological problems, and immunosuppression from the experimental covid-19 treatments.
Bringing a new medicine to market typically takes around ten years, but under intense political pressure, MHRA gave conditional marketing authorisation for the covid-19 treatments after less than one year of clinical trials.
There were numerous published reports and warnings about the risks of MHRA approving the shots on such limited evidence. The manufacturers even said they had expected more safety evidence to be required before approval.
Politicians also failed to heed previous warnings, including the Commons Health Select Committee report in 2004 that warned about Big Pharma’s influence not only on clinical medicine and research but also on patients, regulators, the media, civil servants and politicians; the late withdrawal of the swine flu vaccine in 2009 that resulted in dozens of British children developing the debilitating condition, narcolepsy; and the damning Cumberlege Report in 2020 that detailed many shortcomings at MHRA.
It is therefore not surprising that serious side effects emerged immediately. The AstraZeneca shot was suspended from use for young adults in many countries after only two months, but despite this, MHRA was still attesting to its safety for months afterwards, until the Joint Committee on Vaccination and Immunisation advised that alternatives should be offered to the under-40s. If MHRA had acted at the same time as numerous other regulators, many people would still be alive and uninjured today.
Read the full article in The Light HERE.
Since October 2020, The Light Paper has been publishing a monthly paper ‘The Light’. The May 2023 issue is its 33rd newspaper. The latest issue contains articles that cover who at SAGE is influencing government policy, the data that shows covid injections are unsafe for pregnant women, how control over money will end in slavery, homeschooling, the natural world and the layers of the matrix, why rock bands don’t do their job anymore and much more.
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Featured image: Questions for MHRA, Perseus
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Categories: Breaking News, World News
Steve Kirsch has offered anyone up to 1 million dollars to prove that vaccines work and have been previously trialled, but there have been no takers. It has always been assumed they work, but assumption is not enough evidence to base one’s life on, as with the synthetic mRNA vaccines, for example. It is troubling, to say the least that vaccines are still being injected, when there is a zero probability they do anything positive for the person’s so injected. It is important, in my opinion, that all further vaccines be suspended until a proven safety of them can be established and if that can’t be achieved, then vaccines and the companies which market them, should be held to account and punished accordingly for the injuries and murder their assumptions that vaccines work, have caused to date.
The agreement that they would be immune from prosecution over their vaccines should be made void because of the lies about the trial results of their experimental products.
There is NO FAILURE, it is all purposeful!
Doing the bidding of Bill Gates in return for £huge donations always costs innocent lives.
Anybody shed any light?
There is a new Covid19 vaccine which has been “Emergency approved” again.
This vaccine will have the same purpose, the same Actives and the same incipients, with minute alterations in the sequence of RNA nucleotides. I.e. it easily falls into no “Substantial changes” from the previous vaccine. Ergo it is not a new drug or a new approval.
SO WHY DOES IT NEED TO BE EMERGENCY APPROVED? It should ride on the previous approval.
It is almost 3 years since the original medicines were approved and although they were provisionally emergency approved, Phase III trials were performed and completed earlier this year. If the original vaccine passed phase III acceptance criteria and there were no significant Phase IV surveillance issues, Why does this latest version need to be emergency approved?!?