MST Zoom May 13 2025 | Unmasking the mRNA Nightmare: Dr. Gutschi Reveals What Regulators Hid

Dr. Maria Gutschi, PharmD, BScPhm, RPh, joined us live to share her stunning insights into the manufacturing, regulation, and hidden dangers of the COVID-19 shots. You will not want to miss this rare opportunity to hear from one of Canada's top pharmacological experts, who courageously testified before the National Citizens Inquiry (NCI) about the truth behind the development of these unprecedented gene therapy products.

Who is Dr. Maria Gutschi?

Dr. Gutschi brings over 40 years of frontline pharmaceutical and regulatory experience to this discussion. Her remarkable career includes:

Scientific Officer at the Patented Medicines Prices Review Board — a key regulatory body overseeing pharmaceutical drug safety and pricing in Canada.
Consultant for major national institutions such as Health Canada, the Canadian Pharmacists Association, and the Canadian Forces Health Services.
Clinical pharmacist specializing in complex patient care, infectious disease management, antimicrobial stewardship, and drug assessment.
Author of multiple pharmacy book chapters, including in the Compendium of Therapeutic Choices and Compendium of Therapeutics for Minor Ailments.
Certified Geriatric Pharmacist and Certified Diabetes Educator.

Her expertise in drug development, quality assurance, and safety evaluation is second to none. She is uniquely qualified to assess whether the vaccines met even the most basic standards of pharmaceutical manufacturing — and what she found is deeply alarming.

What Will She Be Speaking About?

Drawing from her meticulous research and insider knowledge, Dr. Gutschi will expose:

How the COVID-19 vaccines were rushed through regulatory approval despite shocking manufacturing defects.
Why the vaccines should have been classified as gene therapies — not traditional vaccines — and what that means for safety standards.
How large-scale commercial production of the vaccines compromised the purity, potency, and safety compared to the original clinical trial products.
The overlooked dangers of mRNA modification, spike protein production, and lipid nanoparticles that persist in the body far longer than claimed.
The startling regulatory failures at Health Canada, the EMA, and the FDA — agencies that abandoned their quality mandates under political pressure.
Real-world impacts: contamination risks, immune system toxicity, and potential long-term consequences that were never properly assessed.

Her testimony at the NCI described the vaccine approval process as a "Good Manufacturing Practices nightmare" and compared the product quality to something "not even fit for veterinary use."

Watch Dr. Gutschi sworn testimony at the NCI Here: https://rumble.com/v49sshz-dr.-luz-maria-gutschi-apr-21-2023-saskatoon-saskatchewan.html

This is not speculation — this is direct testimony based on regulatory documents, leaked confidential files, and decades of professional experience.

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