The laws require multiple consultations in order to prevent our leaders from frivolously invoking emergency powers.
However, in the present instance, the use of "Emergency Use Authorizations" did not conform with US law, in my opinion.
What does the law require in order to allow the use of unlicensed and potentially untested drugs, vaccines, masks and medical tests? Here is the actual language:
§ 360bbb–3. Authorization for medical products for use in emergencies
(b) Declaration of emergency (1) In general
The Secretary may declare an emergency justifying the authorization under this subsection for a product on the basis of—
(A) a determination by the Secretary of Homeland Security that there is a domestic emergency, or a significant potential for a domestic emergency, involving a heightened risk of attack with a specified biological, chemical, radiological, or nuclear agent or agents;
(B) a determination by the Secretary of Defense that there is a military emergency, or a significant potential for a military emergency, involving a heightened risk to United States military forces of attack with a specified biological, chemical, radiological, or nuclear agent or agents; or
(C) a determination by the Secretary of a public health emergency under section 247d of title 42 that affects, or has a significant potential to affect, national security, and that involves a specified biological, chemical, radiological, or nuclear agent or agents, or a specified disease or condition that may be attributable to such agent or agents.
Almost everyone would agree at this point that the Swine Flu lacks "a significant potential to affect national security." Shouldn't that result in an acknowledgment that invoking a law requiring a national security threat is wrong, and we either need a new law for using untested products in purely medical emergencies, or we need to revoke the new Emergency Use Authorizations and rethink our preparedness strategies?
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