Military Operations Monday, Ep. 1: "This company, Pfizer, is now a Defense Dept. contractor."

"They're doing it under the Prep Act, which is for Military preparedness." Attorney Warner Mendenhall


Promo Code: Katherine Watt

Source video link here:

Discussion of Pfizer is around the 32:00 mark.

This is all being managed by the Dept. of Defense, and they’re doing it under the Prep Act, which is for Military preparedness.

Warner Mendenhall, Attorney for Pfizer Whistleblower Brook Jackson

Anyone out there actually think the DOD is actually concerned with your health?

Isn’t is strange how every time they run a table top exercise for a pathogen with their pals Bill and Melinda and Johns Hopkins, the pathogen presents rather quickly into the population?

And their public-private partnerships spring into action with full legal immunity?

Isn’t it strange how they have a dude in North Carolina who has been studying coronaviruses and the heart since the ‘80s? A “gain of function” expert?

Isn’t it strange how patiently, quietly, regardless of team jersey in charge, the Executive Orders and Emergency Authorizations for “public health” continue unabated?

The coup happened a long time ago, fam.

Prep Act:

The Public Readiness and Emergency Preparedness Act (PREP Act) authorizes the Secretary of the Department of Health and Human Services (Secretary) to issue a PREP Act declaration. The declaration provides immunity from liability (except for willful misconduct) for claims:

  • of loss caused, arising out of, relating to, or resulting from administration or use of countermeasures to diseases, threats and conditions

  • determined by the Secretary to constitute a present, or credible risk of a future public health emergency

  • to entities and individuals involved in the development, manufacture, testing, distribution, administration, and use of such countermeasures

A PREP Act declaration is specifically for the purpose of providing immunity from liability, and is different from, and not dependent on, other emergency declarations.

Background: Attorney Warner Mendenhall represents Brook Jackson, Pfizer whistleblower.

Link to Nov. 2, 2021 The British Medical Journal article breaking the story of Pfizer trial malfeasance here. Fired Ventavia Research Group regional director, Brook Jackson sounded the alarm on shenanigans.

Very brave woman.

Katherine Watt digs further.

Bailiwick News
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Comment posted there, revised and expanded here: There was a cystic fibrosis expert on the 2015 Menachery/Baric team that designed SARS-CoV-2, with NIH/NIAID/US-AID and Chinese funding, for maximum transmissibility and lethality: SARS-like Cluster of Circulating Bat Coronaviruses Pose Threat for Human Emergence…
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From KW’s post, updating with my query into the body of the post with more tidbits:


Sage Hana comment: So are all the vaccine manufacturers selected under DOD control or just Pfizer?

KW reply: I believe it’s all of them. Sasha and her team are working their way through the vaxx contracts posted here. BTW, they could use help in that project, if any readers want to help and have the careful reading skills and time to do so. There are primary contracts and subcontracts, but all seem to lead back to DOD at the top. I don’t yet have the specific citation to the contract(s) Sasha mentioned in the Christine Dolan interview, but will check with her by email about it today.

KW follow-up reply:

Checked with Sasha. Turns out Warner Mendenhall was the source of that statement during the interview, so I will check with him asking for the contract citations.

Sasha has a new report out at TrialSite News.

Sasha’s clarifications in response to my question: “If you have time, could you send me the source of your statement that DOD owns the products and controls them from start of manufacture to point of injection?”

“The sources are

1) DOD contracts. They specify delivery to the DOD of all doses, which is not typical for pharmaceutical products. The pharm products must be serialized and distributed through licensed regulated pharmaceutical distributors. If DOD wants to buy some for the military, ok, but why are they buying 100% of the supply?

2) that DOD maintains ownership through to the injection is Warner Mendenhall's statement. I trust him on that, and also it is corroborated by everything I anecdotally know regarding the control of the vials, preventing people from getting access to them, threats, etc.

In a regular drug or device situation, once it's "approved," any licensed professional can order them from distributors and do an independent study.

These injections are not serialized and not available through pharma distribution chain, so the only entity we know that holds them is the DOD.

When a hospital pharmacy orders drugs from distributors, they take possession, and then are responsible for maintaining regulatory compliance per their pharmacy license. The vax centers/hospitals/pharmacies do not buy the injections (so cannot take possession/oversight), they just "administer" them so again, last known purchaser is the DOD.”


Warner Mendenhall reply: Covid Injections: A DOD prototype project. The prototype shot is government property until it is in your body.

Repost of Mendenhall’s September 5 report:

“Hundreds of millions of people have now been subjected to a “prototype” project by the Department of Defense under its Other Transactional Authority. The prototype project includes invention, production, supply chain mechanisms, and injection planning and performance.

The shots are government property until injected. Be careful if you disrupt delivery:

  • Diversion of COVID-19 Vaccines Prohibited (updated 06/11/2021). (expand the links to find this wording, or print.) At this time, all COVID-19 vaccine in the United States has been purchased by the United States Government for administration exclusively through the CDC COVID-19 Vaccination Program. The vaccine and all related ancillary supplies, including the COVID-19 Vaccination Cards, remains U.S. government property until vaccine is administered to the recipient. Inherent in the reference to COVID-19 vaccine remaining property of the United States Government, all USG furnished ancillary materials, including COVID-19 Vaccination Record Cards, have remained property of the United States Government for exclusive use in the CDC COVID-19 Vaccination Program since the program’s inception. This includes COVID-19 Vaccination Record Cards that have been printed by agents on behalf of CDC, including the jurisdictions. USG-provided COVID-19 Vaccination Record Cards remain property of the United States Government until provided to the vaccine recipient following vaccination through the CDC COVID-19 Vaccination Program. The COVID-19 Vaccination Record Cards may not be reproduced by anyone other than authorized jurisdictions or without written permission of CDC. Any use or unauthorized reproduction of the COVID-19 Vaccination Cards outside of the CDC COVID-19 Vaccination Program, or production or use of similar facsimiles of such cards, is prohibited. Any such unauthorized production or use constitutes fraud and is subject to criminal or civil prosecution for violation of 18 U.S.C. § 1001, 42 U.S.C. § 1320b-10, or other relevant federal statutes. COVID-19 vaccination providers are prohibited from selling USG-purchased COVID-19 vaccine (and ancillary materials purchased by the USG for use in the Vaccination Program), soliciting or receiving any inducement, whether direct or indirect, for vaccinating (or providing COVID-19 vaccine to be used for vaccinating) any individual who is not currently eligible to receive COVID-19 vaccine as a member of a group currently authorized under prioritization specified by HHS/CDC/ACIP, the state/territory’s governor or other relevant public health authority, or otherwise diverting COVID-19 vaccine from the CDC COVID-19 Vaccination Program. Such use constitutes fraud and is a violation of the terms of the provider agreement. It shall be cause for immediate termination from the CDC COVID-19 Vaccination Program and criminal or civil prosecution for violation of 18 U.S.C. § 1001 or other relevant federal statutes.

To be compliant with Armed Forces Research Project rules, the project team must ensure that:

  • The project includes a prototype per the statute and the transaction will: “carry out prototype projects that are directly relevant to enhancing the mission effectiveness of military personnel and the supporting platforms, systems, components, or materials proposed to be acquired or developed by the Department of Defense, or to improvement of platforms, systems, components, or materials in use by the armed forces;”

Boy that DOD sure does love us.

Always preoccupied with our health.

Always testing those bioweapons, errr…dangerous viruses, and trying to keep us safe and stuff from the baddies.

Good Lord.

Just nuke us and get it over with.