So the private jab mandates increase. In a worker shortage today, how will this work out if even 5% of the essential workforce move on. Not saying this will happen but it should get interesting.
I read & understand Rappaport’s analysis — but also watched Dr. Malone’s break down the letters such that the new unavailable vaccine is approved while the old EUA vaccine is not. Clearly the paperwork was issued to create obfuscation. I would like to hear the opinion of well respected lawyers that have the skillset necessary to unwrap the legalize within these letters and provide a definitive legal position.
Well, I’m pretty confused about it now. Rappaport seems to understand all the little details and subtleties. But it’s getting to be almost like the US election counts. How could something like this be so complicated?
Children’s Health Defense, Robert Kennedy Jr.’s organization seem to be agreeing with Rappaport’s take on the authorization: there are two uses for the same vaccine, one fully approved (adults, +16) and one still EUA (under 16, third dose recipients). Also, legally, any vial without the Comirnaty label is still EUA only although it is the same thing as what will in later weeks be appearing under the Comirnaty label. Any old labelled vax is still –strictly from a legal standpoint– not approved but still EUA and can be refused on the grounds it is experimental although no different than the approved one which will be coming soon with it’s new label and old vax ingredients.
So, I’d say Rappaport is right and it is approved but only under the new label and new date of manufacture (I guess) which won’t actually occur for a few weeks. After that they can treat the Pfizer C19 vax like any other vaccine regarding mandates. So it’s your future or your job. That’s what’s changed.
My understanding full approval is after the results of Phase 3 trials. Where are those results? I had last heard they were not to be completed until 2022.
It’s confirmed.
So the private jab mandates increase. In a worker shortage today, how will this work out if even 5% of the essential workforce move on. Not saying this will happen but it should get interesting.
Strangely, they haven’t asked for my approval, and that’s the only approval that matters to me!
Right on Strider
I read & understand Rappaport’s analysis — but also watched Dr. Malone’s break down the letters such that the new unavailable vaccine is approved while the old EUA vaccine is not. Clearly the paperwork was issued to create obfuscation. I would like to hear the opinion of well respected lawyers that have the skillset necessary to unwrap the legalize within these letters and provide a definitive legal position.
Well, I’m pretty confused about it now. Rappaport seems to understand all the little details and subtleties. But it’s getting to be almost like the US election counts. How could something like this be so complicated?
Children’s Health Defense, Robert Kennedy Jr.’s organization seem to be agreeing with Rappaport’s take on the authorization: there are two uses for the same vaccine, one fully approved (adults, +16) and one still EUA (under 16, third dose recipients). Also, legally, any vial without the Comirnaty label is still EUA only although it is the same thing as what will in later weeks be appearing under the Comirnaty label. Any old labelled vax is still –strictly from a legal standpoint– not approved but still EUA and can be refused on the grounds it is experimental although no different than the approved one which will be coming soon with it’s new label and old vax ingredients.
So, I’d say Rappaport is right and it is approved but only under the new label and new date of manufacture (I guess) which won’t actually occur for a few weeks. After that they can treat the Pfizer C19 vax like any other vaccine regarding mandates. So it’s your future or your job. That’s what’s changed.
2 Things Mainstream Media Didn’t Tell You About FDA’s Approval of Pfizer Vaccine
https://childrenshealthdefense.org/defender/mainstream-media-fda-approval-pfizer-vaccine/
My understanding full approval is after the results of Phase 3 trials. Where are those results? I had last heard they were not to be completed until 2022.