💉THE POISON NEEDLE AND THE LEGAL SHIELD🛡️ -Here’s How Illegal "Pseudo-Laws" Have Allowed the U.S. Gov’t to Deploy the C-19-Injection Bioweapons on Americans, and Given Legal Immunity to Those Who Administer The Kill Shots (Tweet 1/9)
— Sense Receptor (@SenseReceptor) December 6, 2023
Although many prominent voices in the… pic.twitter.com/Ad87SiF2J5
So what I I've started piecing together is a confusion about the language for drug approvals there are overlapping mutually exclusive pathways that exist and so what I have figured out is that there are three Pathways that we knew before they are all normal regulatory Pathways where we don't have emergency announcements and these normal regulatory Pathways they would include investigational use of products so you can have for example FDA fully approved drugs and it's marketed across the United States and that's the regulatory Mandate of the FDA is to regulate interstate commerce of pharmaceuticals and food so they regulate all these things labeling marketing packaging distribution traceability Obviously good manufacturing practices compliance and they have enforcement power to do recalls if the manufacturer doesn't do it voluntarily manufacturers obviously have an obligation to monitor quality Adverse Events and they have liability if they face liability under this framework.
