Mark A. Hewitt – “Emergency Use Authorization” (EUA) came into prominence with the “Right to Try” law. This law was another way for patients who had been diagnosed with life-threatening diseases, who had tried all approved treatment options and who were unable to participate in a clinical trial, to access certain unapproved treatments.
What is the difference between FDA Approval and Emergency Use Authorization?
“FDA Approval” from the Food and Drug Administration is an independent, scientifically reviewed approval for medical products, drugs and vaccines. Approval is based on substantial clinical data and evidence, the product is deemed safe, effective and able to be produced within federal quality standards.
Continue reading
Adam Andrzejewski – Last year, the National Institutes of Health – Anthony Fauci’s employer – doled out $30 billion in government grants to roughly 56,000 recipients. That largess of taxpayer money buys a lot of favor and clout within the scientific, research, and healthcare industries.
Niamh Harris – During an interview with MSNBC on Wednesday, President Biden’s Chief Medical Adviser admitted that lockdowns were designed to scare people into getting vaccinated.