Criminal Complaint vs. SwissMedic/mRNA Vax
Swiss Lawyer Philipp Kruse provides a comprehensive summary of mRNA "vaccine" regulatory failures and lies
Robert W Malone MD, MS
Apr 02, 2024
On July 14, 2022, Philipp Kruse filed a carefully worded comprehensive legal complaint against the Swiss Regulatory authority known as Swissmedic for their role in enabling deployment of the COVID mRNA “vaccines” into the population of Switzerland. On 28 March 2024, the complaint was refiled with substantial updates and amendments. This complaint provides a comprehensive summary of the case against the official regulatory positions and activities promoted by Swissmedic, which closely parallel those taken by the US FDA, Health Canada, the European Medicines Agency and most other national regulatory authorities.
Swissmedic is the Swiss Agency for Therapeutic Products. More precisely, Swissmedic is the Swiss surveillance authority for medicines and medical devices, and is registered in Bern, Switzerland. Swissmedic fulfills a Swiss federal mission similar to the US HHS Food and Drug Agency (FDA).
Key complaints detailed in this filing include the following criminal acts, which appear to apply equally to many other national regulatory authorities:
Criminal acts performed by Swissmedic
- Initial authorization that breaches the law and duties
- Perpetuation of illegal authorizations that breach the law and duties
- Disregard for all additional indications of risk
- Absence of a "life-threatening or debilitating" disease
- No benefits from ineffective to harmful mRNA injections
- Omission of the most elementary safety and effectiveness tests
- Swissmedic blocked effective alternative treatments
- Benefit-risk analysis – Clearly a negative profile
- Continuing despite an obviously negative benefit-risk ratio
- No product monitoring proportionate to the risks
- Misleading information not proportionate to the risks
- Medical malpractice – lack of information, lack of reports
- Swissmedic out of control and acting to the detriment of the state and the
population
As summarized in his “X” bio (see image above and his academic CV which
can be viewed here), Mr. Kruse is an experienced Swiss and International Law specialist. Having filed this legal complaint, he posted a PDF copy on “X” for download and review, promptly resulting in “X” designating
his account “Temporarily Restricted” due to “unusual activity”.
UPDATE: Due to the censorship of the prior account, Philipp Kruse has now established a new “X” account at @KruseLawyer
I first met Mr. Kruse while visiting Stockholm to lecture on the COVIDcrisis and fifth generation warfare, and he told me of the legal case he was about to file in Switzerland regarding the governmental mismanagement of the response to COVID. Impressed with his knowledge of international law, I invited him to speak at the most recent Senator Johnson hearing in the US Senate regarding his understanding of the legal underpinnings of the proposed WHO pandemic treaty and International Health Regulation modifications. Below is a video of his brief testimony. As you can sense from the video, Mr. Kruse is a very meticulous, detail-oriented and fundamentally conservative (in the classical sense- cautious and non-flamboyant in demeanor and actions) Swiss attorney. He is committed to respect for human rights, but is certainly not a wild-eyed far-right radical. His positions are carefully researched and documented.
Mr. Kruse and his colleagues have addressed their reasons for taking these actions in a press release dated 24 March 2024.
I suggest that the legal complaint which Mr. Kruse has compiled and submitted to Swiss legal authorities is the most comprehensive summary of the regulatory mismanagement and fraud which has taken place at virtually all western national regulatory authorities during the push for mandatory deployment and uptake of the COVID mRNA “vaccines”, and can serve as a template for both other complaints as well as expert witness testimony. Furthermore, I am struck by the parallels between the actions of the Swiss national regulatory authority, the US FDA/CDC, and virtually all other western national regulatory authorities. This strongly suggests close communication and/or collusion among these agencies and their political and bureaucratic State managers during the COVIDcrisis.
With that in mind, I have included key sections from the executive summary of the complaint below. A PDF copy of the full executive summary can be found
here (independent archive) and
here, and the press release together with both the summary and the
full 450 page complaint document can be
found here.
