The vaccine is useless

https://www.newsweek.com/pfizer-merck-covid-pills-could-key-ending-pandemic-1646371


I smell a rat.

The whole vaccine narrative, already wobbly on efficacy, is going down in flames and it’s too big to hide.

Now Pfizer and Merck suddenly each have a vaccine "pill".

These pills supposedly do 3 things:

1. Generate a huge new revenue opportunity for Big Pharma
2. Mask the failing vaccines by distracting the public's attention from one emerging curve under a new one.
3. Here’s the fun part: they totally undermine the pretexts for vaccine mandates or covid vaccination at all.

If a pill supposedly drops risk of serious illness by 89% (remember we were told mRNA vaccines were 95% effective) then why take the risk of shooting up with endless injections (mRNA + regular boosters) that at best afford much less protection for only 6 moths at a time?

We now know that Pfizer fudged the mRNA trials and there's no reason to suppose these pills are all they're cracked up to be, either.
 
Into the Night Soil
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Insult fallacies. Trolling
Click to expand...


What goes around comes around.
 
Desk Inspections, Missed Action Dates Take Place of FDA In-Person Site Visits

As the COVID-19 pandemic continues and in-person activities and travel remain restricted, FDA has been making pharma inspection decisions using rules and policies that are not understood by the industry. The decisions can be a source of consternation for those to be inspected—for example, as part of a new drug approval or for clearing an Official Action Indicated (OAI) status at a manufacturing site.

In some cases, the agency has let an action date lapse and taken no action. In other cases, it has chosen to schedule an inspection after approving a Biologic License Application (BLA) rather than as a prerequisite or to perform a “desk review” of documentation in lieu of an in-person inspection to approve a manufacturing site.

The Field Management Directives (FMD) Manual is the primary vehicle for distributing procedural information/policy on the management of Office of Regulatory Affairs (ORA) field activities. The manual is issued on the authority of the Associate Commissioner for Regulatory Affairs (ACRA) and is intended as internal guidance directed to field managers.

Pharma companies have experienced a variety of FDA inspection alternatives that range from taking no action on impending inspections/decisions to waiving a preapproval or pre-license inspection or choosing to inspect remotely. “There have been some very broad parameters that FDA has placed on what constitutes a mission-critical inspection or a mission-critical application or drug.

Resource Link:

https://redica.com/wp-content/uploads/PREAPPROVAL-INSPECTIONS_7346.832.pdf
 
Vaccine refusals in intelligence agencies raise concerns

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Thousands of intelligence officers could soon face dismissal for failing to comply with the Joe Biden’s vaccine mandate.

Several intelligence agencies had at least 20% of their workforce unvaccinated as of late October. In some agencies, as many as 40% are unvaccinated.

Resistance to the mandate could leave major agencies responsible for national security without some personnel. Intelligence officers are particularly hard to replace due to the highly specialized work they do and the difficulties of completing security clearance checks.

The Office of the Director of National Intelligence declined several requests to provide figures for the intelligence community. The office also would not say what contingency plans are in place in case officers are taken off work due to not complying with the mandate.

Director of National Intelligence Avril Haines declined at a hearing last week to disclose what percentage of the workforce had been vaccinated.

DEMOCRAT members of the House Intelligence Committee say they’re confident that the vaccination mandate will not cause a problem.


https://apnews.com/article/coronavirus-pandemic-health-national-security-intelligence-agencies-chris-stewart-bfff7fc2f8ee0635dd4ae3411c9047eb
 
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