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In the following interview, Canadian consultant pharmacist Maria Gutschi raises concerns about the covid mRNA “vaccines” due to manufacturing issues, contamination and regulatory oversight.
Independent laboratories have verified the presence of plasmid DNA and SV40 contamination in Pfizer-BioNTech and Moderna’s covid injections, exceeding regulatory limits.
Gutschi is calling for the vaccines to be recalled in Canada, reclassified as gene therapies and for independent laboratory studies to investigate mechanisms and adverse events due to the risks outweighing the benefits.
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Earlier today, Sonja Elijah published an interview with Maria Gitshi, formerly a Canadian regulator for drug pricing and hospital pharmacy clinical manager who is now an independent researcher.
During the interview, Gitshi discusses the Chemistry, Manufacturing and Controls (“CMC”) flaws relating to covid “vaccines.” CMC is a crucial activity in drug product development that ensures the quality and consistency of pharmaceutical products throughout their manufacturing process.
You can either listen to the interview on Spotify below or watch the podcast on Sonja Elijah’s Substack page. A transcript of the interview can also be found on Elijah’s Substack page.
Let’s not lose touch…Your Government and Big Tech are actively trying to censor the information reported by The Exposé to serve their own needs. Subscribe now to make sure you receive the latest uncensored news in your inbox…
Call To Halt the Covid-19 mRNA Shots: Pharmacist, Maria Gutschi’s expert critique of mRNA vaccine safety & regulation
By Sonia Elijah
In this compelling interview, consultant pharmacist Maria Gutschi, BScPhm, PharmD, delivers a thorough analysis of the numerous manufacturing “red flags” tied to the covid-19 mRNA injections, spotlighting what she terms Pfizer’s “hard fraud.” She reveals her deep concerns about the mRNA covid-19 vaccines, particularly regarding manufacturing issues, contamination, and regulatory oversight.
Before diving into her insights, it’s important to revisit the DNA/SV40 contamination scandal which underscores the Chemistry, Manufacturing and Controls (“CMC”) concerns raised by Maria in the interview.
Over the last two years, numerous independent labs across the United States, Canada, Germany, Japan, France and more recently the Czech Republic, have verified the presence of plasmid DNA – significantly exceeding the regulatory cap of 10 ng/dose – in Pfizer-BioNTech and Moderna’s covid-19 injections with SV40 promoter/enhancer sequence specifically identified in the Pfizer-BioNTech’s product. This alarming discovery was initially uncovered by Kevin McKernan in April 2023.
My earlier investigations on this scandal can be read below:
- Thou Shalt Not Adulterate: Part 1
- German Study Raises Grave Safety Concerns over BioNTech’s Comirnaty
- Buckhaults: “Proof Plasmid DNA in mRNA vaccine modifies human genome”
Manufacturing Red Flags
In early 2021, Maria Gutschi began her own research on what she calls Moderna and Pfizer-BioNTech’s “gene-therapy products.” While digging through the European Medicine Agency’s EPARs (European Public Assessment Reports) on the mRNA vaccines, she was shocked at its content. Unlike typical EPARs she had reviewed over a decade, this one listed numerous “specific obligations” – legally binding requirements for manufacturers, particularly around manufacturing quality – that were unprecedented in scope and focus. Maria emphasised that for biologics like mRNA vaccines, “the process is the product,” meaning manufacturing flaws directly affect safety and efficacy.
Whenever you manufacture a biologic, it is always a problem getting the purity right, because the process is the product.
The process on how you make a biological is what you end up with.
The EPAR highlighted significant manufacturing concerns, including:
- Purity and Consistency: The EMA flagged multiple unresolved issues, such as ensuring the spike protein produced was authentic and consistent across batches.
- Specific Obligations: Unlike usual clinical trial follow-ups, five or six obligations focused on manufacturing, which Maria found unusual and indicative of deeper problems.
DNA Contamination Findings
Maria became involved in investigating DNA contamination in the vaccine vials. Notably, she was co-author of the preprint paper by Speicher et al., published in October 2023, which confirmed Kevin McKernan’s troubling findings of DNA/SV40 contamination in the Moderna and Pfizer-BioNTech vials vastly exceeding the regulatory cap. The presence of plasmid DNA with regulatory sequences (e.g., SV40 in Pfizer) and lipid nanoparticles (“LNPs”) enabling cellular entry raised concerns about genomic integration and biological activity.
Other Key Issues Explored
1. Blotgate Scandal: Maria discussed how BioNTech dismissed Western blot anomalies (unusual spike protein sizes) as glycosylation (sugar attachments), a claim the EMA accepted without sufficient follow-up. This specific obligation remains unmet as of 2025.
2. Ribosomal Frameshifting: A Cambridge study (December 2023) confirmed mRNA vaccines could cause frameshifting, leading to aberrant proteins with unknown effects (e.g., toxicity, autoimmunity).
3. SV40 Contamination: Found in Pfizer vaccines, the SV40 promoter/enhancer sequence (with an origin of replication) can amplify itself, block the p53 tumour suppressor gene and potentially promote oncogenes, raising cancer risks. Health Canada was shocked by this undisclosed contamination but took no decisive action after Pfizer resisted accountability.
4. Lipid Nanoparticles: Maria criticised their classification as excipients (inactive ingredients), noting their reactive nature and ability to deliver contaminants (DNA, RNA, metals) into cells, bypassing normal regulatory mechanisms – a “Trojan horse” effect increasing risks like DNA integration.
Canadian Open Letter
Maria has spearheaded an open letter that will be sent on 31 March to Canadian MPs, senators and provincial health officers, highlighting:
Health Canada’s Findings: FOI requests (ATIPs) revealed regulators’ concerns about DNA variability, SV40, LNPs, frameshifting and IgG4 immune tolerance, yet action was stifled.
Demands: Recall the vaccines due to risk outweighing benefits, reclassify them as gene therapies (not vaccines), and fund independent lab studies to investigate mechanisms and adverse events.
SV40 Cover-Up: Pfizer’s failure to disclose SV40 violated WHO guidelines, constituting “hard fraud,” with Health Canada’s response squashed internally despite initial efforts to address it.
Further reading:
- 2025 03 17 En Letter Of Concern Tobesentmar31 V2 Download HERE and 2025 03 17 Fr Lettre Ouverte Dinquietude Tobesentmar31 V2 Download HERE.
- Call to Halt-19: A Canadian letter to halt the mRNA vaccines, Maria Gutschi, 18 March 2025
Featured image: Maria Gutschi (left) and Sonja Elijah (right)
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“Health Canada’s Findings: FOI requests (ATIPs) revealed regulators’ concerns about DNA variability, SV40, LNPs, frameshifting and IgG4 immune tolerance, yet action was stifled”
I mentioned Ig4 backbones being used in chimeric antibodies to avoid the immune system last week. Ig4 is pathogenic in large amounts and can present as blisters on mucosal linings, such as Bulbous Pemphigoid. Here’s a real world example:
“Background AK117 is a novel humanized IgG4 monoclonal antibody (mAb) targeting CD47, a macrophage immune checkpoint and ‘don’t eat me’ signal that allows tumor cells to evade immune destruction by phagocytic cells.”
https://www.researchgate.net/publication/346801070_384_A_Phase_1_study_to_evaluate_the_safety_PK_and_antitumor_activity_of_AK117_an_anti-CD47_monoclonal_antibody_in_subjects_with_relapsedrefractory_advanced_or_metastatic_solid_tumors_or_lymphomas
Frameshifting is a technique typically used to print reporter genes, such as Luciferase, but can be used to print any small ~72-100’ish bp sized protein. Larger proteins can be printed out or the IRES. The IRES is capable of printing multiple proteins, so long as cellular resources permit.
There is no DNA “contamination”; the system is literally designed for it.
For an off-topic happier moment, I attached Superman:
Excuse me: “reclassify them as gene therapies”???These ARE GENE THERAPIES, ALWAYS WERE!!!
Some are just VERY late in grasping essentials.
You would have to be dead and possibly embalmed not to notice how sick and miserable so many people are. Everywhere I go people are sick, When I ask if they have been jabbed they all have. They have no idea the factors that could be contributing. The man made stuff in the air, in the water, in their medications, in the jab. The Electromagnetic None of it makes any sense. Someone said to me last week (and they had had 6 surgeries in the past 3 years, and were not recovering) that they would rather die from a jab than have measles – Oh yes we have done a hornswaggling job. People only speak in non-sequitors – pardon,….dead is dead. like saying I’d rather die of MAID than chance getting sick. And are you sick? What are you counting on to keep you well? Your diet? your worry, fear and anxiety? the information on your screens and conveyed directly into your head via ear buds, Your apple phone, telling you how many steps you’ve taken today? Your prayers? Your ignorance? How is it working? Are you feeling good, energized, creative, excited about life. Thank you. Looking forward to this upcoming event. . Let’s stop the prevarication, the arguing about unimporant details. Force fields clashing with our inner electricity? important details like what is in the ingredients and instead take seriously what we see all around us. No one is feeling good. Let’s stop polluting our bodies The doctor who wrote last week clarifying That’s what Doctors do – fill little children with powerful drugs when they have a rash. Here’s to us. Magical, alert, questioning us.
I wish they wouldnt use the term therapy which surely implies that something is beneficial. cant they find some other tem for it?
Hi mcc, the problem with creating too many terms is that it ends up confusing people. It is one of the tactics that psychological warfare uses, to keep making up terms or misuse terms to confuse people. Sometimes the most effective communication is to stick to terms that people understand or can easily understand.
For example, everyone understands what a vaccine is: its an injection. So, calling it an injection is okay because people understand that a vaccine is an injection. But once we start with terms such as modRNA injection etc some people start to lose the understanding of what it is we’re referring to. Although we have always known that Pfizer and Moderna’s covid vaccines are modRNA (modified RNA), for a lot of people its not immediately identifiable so they lose interest or will simply scroll on by. We shouldn’t need to refer to some sort of new dictionary to interpret what people are saying.
In short what I’m saying is, we can shoot ourselves in the foot by trying to come up with new terms to describe things. The key is to use familiar terms that are used every day to describe things and then describe what those terms actually mean. So for example, all vaccines are bad for different reasons depending if they’re DNA, mRNA, modRNA, viral vector, “new” vaccines, “traditional” vaccines etc so its fine to call them “vaccines” and so give all vaccines a bad wrap.
Here’s a simple definition using commonly understood terminology to show what I mean: All vaccines contain viruses. The viruses are in the vaccines. That is how they are infecting people, by injecting viruses into them. In short, vaccine is doublespeak for virus. If we replace “virus” and “vaccine” with uncommon words, not immediately understood by most, does it make much sense to the average person?
[…] Canadian pharmacist: Halt covid vaccinations and reclassify them as gene therapies […]
thank you Maria Gutschi. YOU are a hero and we appreciate you standing up for us.
[…] by Rhoda Wilson, Expose News: […]
[…] V tomto působivém rozhovoru poskytuje farmaceutická konzultantka Maria Gutschi , BScPhm, PharmD, důkladnou analýzu četných výrobních vad spojených s injekcemi mRNA covid-19 a poukazuje na to, co nazývá „tvrdým podvodem společnosti Pfizer.“ […]
Supreme Court Rules Family Can Sue over Teen’s Unwanted Coronavirus Vaccine
When the clinic was unable to reach his mother, a worker instructed another to “give it to him anyway,”
https://www.breitbart.com/education/2025/03/24/video-nc-supreme-court-rules-family-can-sue-over-teens-unwanted-coronavirus-vaccine/
[…] Related: Canadian pharmacist: Halt covid vaccinations and reclassify them as gene therapies […]
[…] Înrudite: Farmacistul canadian: opriți vaccinările covid și reclasificați -le ca terapii genice […]
[…] Relatif: Pharmacien canadien: Halte aux vaccinations et reclasse-les en thérapies géniques […]