Brutally True. 😢

"Targeting the Davos, Switzerland-based World Economic Forum and its devotees among global political leaders, attorney Reiner Fuellmich says they are guilty of crimes against humanity for their perpetration of COVID-response policies that led to forced shutdowns, destroyed businesses, impoverished families, broken lives and a spike in suicide rates.
He has formed the German Corona Investigative Committee to pursue civil charges against the main perpetrators, among them being the head of the United Nations World Health Organization Dr. Tedros Adhanom. He hopes a successful class-action lawsuit will also lead to criminal charges."
https://humansarefree.com/2021/03/legal-team-wants-second-nuremberg-tribunal-to-try-global-lockdown-promoters-for-crimes-against-humanity.html

Is it a coincidence I am suspended from twitter for no valid reason the week they knew this letter was going to come out, and my appeal has received no response? Is it a coincidence that a fake Mike Yeadon account appeared on twitter the day before just as I was sharing Mike's posts from Telegram to twitter?

BOT is doing good work out there. 🤖 https://twitter.com/robinmonottibot/status/1369715800177848320?s=19

The Truth Behind The Vaccine Trials - Documentary Film 2021
https://rumble.com/vebrjv-the-truth-behind-the-vaccine-trials-documentary-film-2021.html

FDA Approval requires minimum 1 year of Phase 3 clinical trials. Phase 2 trials of Pfizer completed on 19th June 2020, which means Phase 3 needs to last at the very least until 19th June 2021 to be even considered for approval by the FDA.

At the same time, the EUA authorization is only valid if there is a pandemic emergency.

Which means they need to keep the "pandemic" going at least until June. That is why roadmaps to reopening are so slow.

https://www.fda.gov/patients/drug-development-process/step-3-clinical-research#Clinical_Research_Phase_Studies

https://www.patreon.com/robinmonotti

⚠️WARNING⚠️
https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/treatments-vaccines/vaccines-covid-19/covid-19-vaccines-studies-approval#what-studies-are-needed-after-approval?-section

⚠️In the EU, clinical studies approval timing laws are under the rules of the country the studies take place in, not under EU EMA rules⚠️
https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/treatments-vaccines/vaccines-covid-19/covid-19-vaccines-studies-approval#what-types-of-studies-are-needed-to-approve-a-covid-19-vaccine?-section

Mike Yeadon: "This is completely contrary to medical ethics, without any question.
I dismiss all false equivalencies with influenza, for example.
Even trialling new technology medical interventions at scale is reckless enough.
Administering these to anyone not at risk, arguing that they’ll help protect others, is wrong on a number of levels.
Though this is part of the rationale for flu mist vaccination in kids, it’s often forgotten that young kids are at much greater risk from flu than are healthy adults (until quite late in life).
In this basis, I’d like to see the ethical review board’s conversations ahead of such paediatric vaccination trials."

EU: Even the efficacy studies are ongoing: "The efficacy studies may continue for two years or more" https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/treatments-vaccines/vaccines-covid-19/covid-19-vaccines-studies-approval#what-types-of-studies-are-needed-to-approve-a-covid-19-vaccine?-section

The problem here is the small amount of people who caught the disease even in the placebo group and the case definition they used: 1 positive RT-PCR test at astronomically high cycle thresholds and one mild symptom which could be a headache.
https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/treatments-vaccines/vaccines-covid-19/covid-19-vaccines-studies-approval#what-types-of-studies-are-needed-to-approve-a-covid-19-vaccine?-section

⚠️ EU EMA confirms 1 year is required for safety trials, that is why they are pushing the pandemic into late June ⚠️
https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/treatments-vaccines/vaccines-covid-19/covid-19-vaccines-studies-approval#what-types-of-studies-are-needed-to-approve-a-covid-19-vaccine?-section

Standard vaccine timing scales

Covid19 vaccine timescale (EU)

The US gives an Emergency Use Authorization (EUA), whereas the EU gives a Conditional Marketing Authorization (CMA). ⚠️ NONE OF THESE ARE ACTUAL VACCINE APPROVALS ⚠️
https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/treatments-vaccines/vaccines-covid-19/covid-19-vaccines-development-evaluation-approval-monitoring

ema-considerations-covid-19-vaccine-approval_en.pdf

HERE WE GO, THIS IS WHY THEY NEED THE PANDEMIC GOING AT LEAST TIL LATE JUNE. CURRENT VACCINE AUTHORIZATION (NOT APPROVAL) IS TEMPORARY PENDING CONCLUSION OF CLINICAL SAFETY TRIALS WHICH MUST BE AT LEAST ONE YEAR IN DURATION. NO PANDEMIC AND AUTHORIZATION CAN BE CHALLENGED.

ICMRA JULY 2020:

"Follow-up of study participants for COVID-19 outcomes should be long enough (i.e., 1 year or longer post-vaccination) to evaluate safety, duration of immune response and risk of disease enhancement as antibody titers wane."

ICMRA SARS-CoV-2 Vaccines Workshop #2 - Summary | International Coalition of Medicines Regulatory Authorities (ICMRA)
http://www.icmra.info/drupal/news/22june2020/summary

https://www.patreon.com/robinmonotti

OUR BEST WEAPON IS THE EDUCATION OF THE GENERAL PUBLIC. WE HAVE AN ACTIVE ROLE IN THIS. WE ARE NOT PASSIVE BYSTANDERS.