Quick question – if there is no longer a public health emergency, how can the FDA/CDC authorize the new booster under “Emergency Use Authorization”?
From here:
COVID-19 Public Health Emergency (PHE) | HHS.gov
“Based on current COVID-19 trends, the Department of Health and Human Services (HHS) is planning for the federal Public Health Emergency (PHE) for COVID-19, declared under Section 319 of the Public Health Service (PHS) Act, to expire at the end of the day on May 11, 2023.”
And here:
“This Memorandum of Understanding (MOU) between the Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) provides a framework for coordination and collaborative efforts between these two agencies, which are both components of the Department of Health and Human Services.”
Am I missing something? Perhaps the EUA is an extension of an existing EUA, not a new one?
Onwards!
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The ONLY way to stop this lethal foolishness to all of us....is to throw the bumps OUT as soon as possible from the WH and all senior position in this Govt who continue to force things upon us. Whether you are Independent or MAGA or even a Dem mother who wants no lethal chemicals in their kids....they all should realize we need our country back.
The Trillion Dollar Question.