It's promising that there will be slightly higher regulatory standards for the Omicron vaccine: clinical trial in humans must be completed before approval and clinical trial data must be submitted at the same time, i.e. no 75-year delays.
> the debate appears to have shifted with the European Medicines Agency (EMA) saying on Friday that international regulators now preferred clinical studies to be carried out before approval of a new vaccine ... Inclusion of clinical trial data in the regulatory filings may have an impact on the delivery of initial batches.
A major British medical journal just demanded that the raw trial data be released - but will it even be untampered with - like the Maddie De Garay situation insinuates happens widespread since there were no, and still no, government health agencies who have sounded an alarm - or caught it and put a hold on the vaccine release for different age groups until uncompromised trials were completed?
The system capture here is so obvious it's blinding.
There are many nested challenges, e.g. system/regulatory capture is not new, but can you think of a single historical example with pervasive lockstep censorship across media, industry and government in multiple countries? Did government relief/stimulus funding distort incentives for health outcomes, e.g. ineffective high-fee ventilators vs. early treatment with existing drugs?
Even in the face of lockstep censorship, as truth/facts surfaced in 2020-2021, why did no organized presentation achieve widespread public visibility? Without an accurate threat model (e.g. infiltration of health freedom groups, https://ccsfreedom.org/), truth will not be sufficient to prevail against organized opposition.
https://youtu.be/L2GKPYzL_JQ - "How many more adverse effects have been covered up during the trials? - Maddie de Garay's story."