European Commission regulations implementing the global pharma-military kill box

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In the Maria Zeee interview, I said that recently, legal researchers in Europe had located some of the mechanisms through which the global bioterrorism/medical martial law program functions to surveil, capture, control and kill people in European countries.

Some of the mechanisms can be found in corporate contracts signed between European governments and pharma-bioweapons manufacturers.

See, for example, Sasha Latypova’s reporting about the contents of emails between key European war criminals.

…Ursula von der Leyen – EU Commissioner, whose achievements include negotiating incredible predatory Pfizer supply contracts on behalf of all EU Member States by text messages with Pfizer CEO Albert Bourla. In these contracts the EU countries had to put up state assets as collateral, waive all quality control, importation and consumer protection laws and give up national sovereignty – i.e., not allowed to change legislation with respect to vaccine liability by their own parliaments? The predatory contracts that were completely redacted to protect so-called “Pfizer commercial interests”…

There are a bunch of acronyms used, the most relevant are “EC” = European Commission, “MS” = Member States, “EP”=European Parliament.

The key sentence is that Ursula isprepared to call relevant health ministers personally to avoid the use of Article 5 (2).”

What is this about? Article 5 (2) refers to “Article 5 (2) of Directive 2001/83” – Emergency use authorization in a European Member State, given by each of the Member States separately in their own countries. [“Article 5 (2). Member States may temporarily authorise the distribution of an unauthorised medicinal product in response to the suspected or confirmed spread of pathogenic agents, toxins, chemical agents or nuclear radiation any of which could cause harm.]

CMA is a Conditional Market Authorization which is issued by the EMA for all EU members simultaneously…

The problem is that Ursula never meant to fulfill these promises, and at any rate, it is not possible to produce the mRNA “vaccines” to the safety, efficacy and manufacturing quality required of pharmaceuticals.

What Ursula really needed from this process was to tie all the European Member States together in a pact by promising a “robust” CMA, so that they could not have an independent authority over the shots distributed in their countries…

Article 5 path would have meant each MS could authorize the product, and would then have the power to revoke the authorization if any problems detected.

Article 5 also provides a liability waiver to the manufacturer, however makes it impossible to mandate the product.

With the CMA route none of the member states could exercise the independent decision making, and so she would be able to then force them all into the same, insane and almost completely redacted Pfizer, Moderna and AstraZeneca contracts, which waived all liability anyway, and further prohibited the countries to change their own laws in regard to the liability…”

Other mechanisms are embedded in European Commission regulations about “countermeasures” authorizations and financing mechanisms, a paper trail located recently by a legal researcher who works in one of the EU member-states.

Below is a chronological reorganization and expansion of the raw email content Sasha posted last week:

Bailiwick readers in Europe may find it useful to start by downloading and carefully reading the documents below (the English versions of which I’ve uploaded to my Bailiwick WordPress backup site), and then explore Eur-Lex, the European Union’s database of legal documents, which has translations of the documents into member-state languages.

Knowing the names, numbers and contents of the regulations will help in your efforts to educate and mobilize social and political momentum for your government officials to pass blocking legislation at the nation-state level; repeal the kill box laws at the EU level; and/or withdraw your country from the European Union.

The EU provisions correspond with the US provisions related to “medical countermeasures” and establishment of home- and business-based concentration camps (prohibition of free human association, commerce and movement within countries and across borders) in case of “natural or man-made disaster”

To recap, the American biomedical police state — controlled by the World Health Organization operating as the military branch of the Bank for International Settlements — came into force through statutes passed by the US Congress; executive orders issued by US Presidents; administrative/Cabinet agency regulations published in the Federal Register; and state and local versions of same. See footnoted executive summary of American Domestic Bioterrorism Program.

The European biomedical police state came into force through analogous regulations passed by the European Parliament and the Council of the European Union, published in the Official Journal of the European Union.

Prior to locating these European Commission regulations, many attorneys in the EU member states thought that bioweapons regulation (falsely identified by government officials as ‘vaccine’-regulation) was covered by provisions of EU law governing Conditional Marketing Authorization (CMA).

Turns out, that is not the case.

The backbone of the EU biomedical police state is comprised of provisions outlined below.

These are the rules the BIS/WHO puppets in the European Union have passed, to support their joint program to poison you and your kids behind the mask of public health, and force you to finance the mass murder program as well.

1998/09/24  – Council Decision No. 2119/98/EC – Setting up a network for the epidemiological surveillance and control of communicable diseases in the Community.

Article 1.

The objective of this Decision is to set up a network at European Community level to promote cooperation and coordination between…

Read full story: European Commission regulations implementing the global pharma-military kill box


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