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had the pleasure of interviewing Dr Robert Malone, inventor of mRNA technology and vaccine expert, for the second time. Malone revealed the alarming counts of censorship by the scientific journals and the major conflicts of interest at play. He exposed “another way the pharmaceutical industry can exert influence by bending the law.” Dr Malone spoke how Covid vaccine companies are being given special treatment by the FDA and that “the manipulation of the data is occurring on multiple levels.” He spoke about the strong disincentives for doctors to report vaccine adverse events to VAERS and explained the term “plausible deniability” in the context of why the CDC denies that there are any vaccine-related deaths.

1131 children aged 12–15-years-old were enrolled in Pfizer’s clinical trial of their mRNA based Covid vaccine. Maddie was one of them. Stephanie, her mother, shares Maddie’s heart-wrenching story with Sonia Elijah for Trial Site News.

Dr Peter McCullough, MD, one of the most cited physicians in the world, an eminent practitioner of internal medicine, a cardiologist and epidemiologist, co-wrote a report with Dr Jessica Rose, Ph.D., a virologist and epidemiologist in Canada, called ‘A Report on Myocarditis Adverse Events in the U.S. Vaccine Adverse Events Reporting System (VAERS) in Association with COVID-19 Injectable Biological Products.’

In a riveting interview, Shabnam Palesa Mohamed engages scientist Shimon Yanowitz about strange visuals in the blood of C19 vaccinated people. He presents evidence, from various experts, of self-assembling particles, synthetic organisms, ribbons and tubes, AI circuits, sharp crystalline, and graphene oxide. Yanowitz also shows his own blood, with strange anomalies, and invites experts to examine blood of vaccinated people for themselves. Will this evidence be seen by police, courts, or intelligence? About Shimon Yanowitz: Independent scientist and researcher specialising in Electrical Engineering (computer-vision, microscopy, electromagnetic radiation and 5G, microelectronics). For the past 3 years, he researched nanotechnology and its potential role in the C19 injections, and then tested the injections with optical and electron microscopy, sharing findings in the blood of both jabbed and unjabbed. He participates in international groups who are involved with C19 issues in general and the injections in particular. Resources: IJVTPR Journal article: "Between July 2021 and August 2022, evidence of undisclosed ingredients in the COVID-19 “vaccines” was published by at least 26 researchers/research teams in 16 different countries across five continents using spectroscopic and microscopic analysis. Despite operating largely independently of one another, their findings are remarkably similar and highlight the clear and present danger that the world’s population has been lied to regarding the contents of the COVID-19 “vaccines”. This raises grave questions about the true purpose of the dangerous experimental injections that have so far been shot into 5.33 billion people (over two thirds of the human race), including children, apparently without their informed consent regarding the contents. Surprise findings include sharp-edged geometric structures, fibrous or tube-like structures, crystalline formations, “microbubbles”, and possible self-assembling nanotechnology. The blood of people who have received one or more COVID-19 “vaccines” appears, in case after case, to contain foreign bodies and to be seriously degraded, with red blood cells typically in Rouleaux formation. Taken together, these 26 studies make a powerful case for the full force of scientific investigation to be brought to bear on the COVID-19 “vaccine” contents. If the findings of these 26 studies are confirmed, then the political implications are nothing short of revolutionary: a global crime against humanity has been committed, in which every government, every regulator, every establishment media organization, and all the professions have been complicit." - https://www.ijvtpr.com/index.php/IJVTPR/article/view/52 Summary article: https://www.trialsitenews.com/a/direct-microscopic-examination-of-pfizers-covid-19-injections-contents-of-the-vials-are-interacting-with-electromagnetic-fields.-0d437119 Connect with TSN: Website: www.trialstenews.com Youtube: Rumble: Telegram: t.me/trialsitenews Twitter: Instagram: Facebook: #TrialsiteNews #TSN #Health #Science #Evidence #Vaccines #Vials #Blood

“To think we’re going to boost our way out of this- is preposterous.” Dr David Wiseman I had the fortunate opportunity of interviewing Dr David Wiseman, a PhD research Bio scientist, former Johnson & Johnson clinical trial head-researcher and journal peer reviewer. Dr Wiseman with his small but dedicated team have masterfully compiled a series of slides analysing the data from Israel, UK, Denmark and Canada for the Pfizer-BioNTech Covid vaccine comparing vaccine effectiveness of the primary series of vaccination (dose 1 and 2) with the booster. What he revealed in his analysis of the data was highly alarming and raised many red flags of negative vaccine efficacy and its implications- where the vaccines are doing more harm than good.

Sonia Elijah of Trial Site News speaks to: Kim Witczak, leading international drug safety advocate and consumer representative on the FDA’s advisory committee. Following the tragic event of her husband, Woody’s, suicide shortly after taking Pfizer’s anti-depressant medication, Zoloft, Wiczak filed a lawsuit against the behemoth drug company when she discovered, suicide was a known side effect, resulting in Pfizer adding a warning label issued as a black box warning by the FDA. Witczak speaks about her extensive research on the Big Pharma’s insidious influence over media; the legal system; medical journals and academic institutions to name but a few, culminating in her generating a map called the Spider’s Web. Heather Hudson, mother of a severely mRNA vaccine injured young man, turned medical researcher, speaks openly about her son’s injuries (pulmonary embolisms, blood clotting and neuropathy) and how his condition, anti-phospholipid syndrome, which causes the immune system to attack the body’s own cells, is related to the lipid nanoparticles found in the Pfizer-BioNTech mRNA Covid-19 vaccine, particularly the modified phospholipids. Dr Eduardo Balbona helped save Cody, Heather’s son, when he was on the brink of death, and when all the other doctors turned him away. Dr Balbona ran critical tests that showed the modified phospholipids found in the mRNA vaccine, caused Cody’s life-altering injuries. Both Dr Balbona and Hudson’s ground-breaking research has led to the discovery of how the injectable modified phospholipids can cause serious adverse events in the human body.

An interview with Dr. Geert Vanden Bossche, a leading virologist and international vaccine expert. Before taking an R&D role for several well-known vaccine companies, he worked for fifteen years in academia. Dr Geert was also the former senior program officer in vaccine discovery for the Bill and Melinda Gates Foundation and the former senior Ebola Program manager for GAVI, Global Alliance for Vaccines and Immunization.

The Senate Homeland Security and Governmental Affairs Committee heard from medical professionals who advocate for alternative coronavirus treatments and mitigation measures than those at the National Institutes of Health, Centers for Disease Control and Prevention, and World Health Organization. Unexpected Drama emerged as Ranking Member Gary Peters in his opening statement denounced the hearing and castigated the Doctors before they even had a chance to speak. Hear Doctor Pierre Kory of the FLCCC respond in a phone interview with TrialSite News. TrialSite News Original Article On This Story: https://trialsitenews.com/senate-homeland-security-committee-holds-hearing-on-the-covid-19-pandemic-learn-about-promise-of-ivermectin/ To learn more about the FLCCC Alliance follow the link below: https://covid19criticalcare.com/ C-SPAN3 Full Video of the Hearing: https://www.c-span.org/video/?507035-1/medical-response-covid-19 #ivermectin #covid-19 #senate hearing

In an interview with TrialSite News, Edward Dowd describes how the FDA should never have approved Pfizer's COVID vaccine, reveals alarming mortality data and explains how investors on Wall Street could be the key to turning things around. Edward Dowd was a managing director with BlackRock from 2002 to 2012 and has spent most of his career on Wall Street. He has worked with HSBC, Donaldson, Lufkin & Jenrette, Independent Investments and managed a $14 billion equity portfolio for Black Rock. He is currently a consultant for Symphonic Capital and is working to expose the fraud he believes is happening with Pfizer and Moderna, and how this affects financial markets, Wall Street and public health.

FDA's Dr Peter Marks says the 4th Booster Dose was a "Stop-Gap" measure to buy time for the next booster.

In this first episode of Whistleblower, Shabnam Palesa Mohamed speaks with a veteran registered nurse who has chosen to speak out because she believe medical practices "are killing people" and "we need to save lives". To protect patients, 'Susan' shares harrowing experiences of C19 patient trauma and post jab injuries including heart attacks, brain damage and death. According to Susan, 300 C19 patients who died could have been saved had the hospital changed their protocols and avoided drugs like Midozolam. Adding to the impact, is the targeting and victimisation of staff who dare to speak out for their patients.

Hedley Rees is a drug development expert and author. Rees is the Managing Consultant at PharmaFlowLimited, a UK-based consultancy specializing in supply chain management within the pharmaceutical and life science sectors. Clients range from large pharmaceutical companies to emerging biotech, and also include investors, lawyers, other consultancies, facility design and build specialists, and third-party logistics providers. Assignments span preclinical, clinical, and commercial supply chains up to complex multi-product networks covering global territories.

Join The Conversation! | https://trialsitenews.com/ Sonia Elijah from Trial Site News interviews Dr David Wiseman, who critically evaluates the "imprecise and unstable" data that the FDA relied on to authorize the Pfizer and Moderna COVID-19 vaccines for children as young as six months old. Wiseman also provides an illuminating review of the pivotal VRBPAC meeting of June 14-15, 2022. Referenced FDA Video: Vaccines and Related Biological Products Advisory Committee – 6/15/2022 | https://www.youtube.com/watch?v=Ixm4UmldTGQ

In this must watch episode, Shabnam Palesa Mohamed engages Adv Dipali Ojha, attorney Diane Protat, and journalist Xavier Azalbert about legal actions against controversial billionaire Bill Gates. In India, he is being sued $125 million for a vaccine-related death of a 32 year old doctor. In France, he is being sued for misrepresentation and defamation while speaking live on French television. All three are determined to ensure that vaccine oligarch Gates faces justice for his role in causing, censoring and profiteering off vaccine related harm. Time is running out as the flood gates of litigation open. We also engage: - Other vaccine deaths and compensation in India / France - Whether the BMGF-funded Serum Institute can be trusted - A campaign to highlight menstruation-related adverse effects - The role of independent media vs the role of conflicted media - The role of social media in the 'safe and effective' PR campaign - Conflicts of interest, concentration of power, and corporate monopolies Related: * https://www.trialsitenews.com/a/allegations-of-bill-gates-and-the-who-influencing-vaccine-only-protocols * https://www.trialsitenews.com/a/gates-proposes-a-1bn-solution-to-make-covid-the-last-pandemic-ea51475c * https://www.trialsitenews.com/a/serum-institute-of-india-chief-recommends-governments-shield-pharma-from-vaccine-lawsuits Video: Rumble and Youtube links Website: www.TrialSiteNews.com Telegram: @TrialSiteNews Twitter: @TrialSiteNews #TrialSiteNews #TSN #Health #Science #Law #Justice #India #France #BillGates

Dr. David Wiseman talks about Molnupiravir and FDA Advisory Committee with Dr. Erin

Part 1 of my investigative series focused on the sudden removal of a published, peer-reviewed paper on vaccine-induced myocarditis based on US VAERS data, authored by Dr Peter McCullough, MD, MPH, and Dr Jessica Rose Ph.D., by Elsevier and Current Problems in Cardiology. Part 2 centers on my revelatory interview with Dr Pierre Kory MD, an expert critical care physician and pulmonary (lung) specialist. Dr Kory is a world pioneer in the use of ultrasound in the diagnosis and treatment of critically ill patients. He is also the co-founder and president of FLCCC (Frontline Covid-19 Critical Care Alliance).

Sonia Elijah interviews My interview with Prof Norman Fenton was highly revealing you can watch it here. Fenton, who has a PhD in Mathematics, is professor of Risk Information Management at Queen Mary, University of London. He co-authored a paper along with eight others including: Martin Neil, Jessica Rose, Clare Craig, Jonathan Engler, Joel Smalley, Scott Mclachlan, Joshua Guetzkow and Dan Russell. The paper, entitled, ‘Official mortality data for England suggest systematic miscategorisation of vaccine status and uncertain effectiveness of Covid-19 vaccination’ was published early December 2021, as a preprint on ResearchGate. Their paper was an in-depth analysis of the UK ONS report, ‘Deaths involving Covid-19 by vaccination status, England: deaths occurring between 2 January and 24 September 2021.’

In this must watch episode of CATalsyt, Shabnam Palesa Mohamed interviews three South African doctors about their letter of concern to SAHPRA, SAMA and the HPSCA. The letter details what they and a growing number of medical professionals are seeing in people who take the C19 jabs. Dr Erika Drews, Dr Frank Muller and Dr Ami Muller also speak about patients being ignored when they try to report negative effects, and when they seek treatment. The doctors are equally candid about censorship, jab mandates, and medical discrimination. Are they afraid of consequences? Find out.

Dr. Erin Stair discusses with Dr. Robert Malone about the COVID-19 Spike Protein vs the Spike Protein produced by the COVID-19 Vaccines and more.

Is 'safe and effective' fraudulent misrepresentation? Is censorship of science misrepresentation? Is non-disclosure of conflicts of interest fraud through omission? What about uninformed consent? In this first episode of Law vs Science, Shabnam Palesa Mohamed engages multi-skilled scientist Dr Jessica Rose, veteran OBGYN expert Dr James Thorpe, and clinical researcher and Pfizer whistle-blower Brook Jackson on the strongest evidence of fraud in the C19 jab trial. Each with uncensored perspectives, these experts believe that fraud, misrepresentation, negligence, and omission continues to happen, and must result in accountability. But from whom? Who is 'the government'? And what is the dire premonition about growing public anger? Website: www.trialsitenews.com Telegram: t.me/TrialSiteNews #LawVsScience #TrialsiteNews #Uncensored #HealthScience

I am learning from Dr. Michael Palmer, a physician and microbiologist from Canada about mechanisms of tissue damage by spike protein in the mRNA injections. We are looking at histopathology slides from a German pathologist Dr. Burkhard who performed autopsies on several vaccine victims.

Katherine is an independent journalist and a legal researcher who has created a meticulously cited and sourced reference on her substack (Bailiwick News). Katherine has uncovered specific changes to the US laws that have over the years lead to the current events which she characterizes as a domestic bioterrorism and mass murder masquerading as a public health emergency response. We discuss the key aspects of law that enabled subversion of people's Constitutional rights, use of fear and propaganda and other unlawful acts by the US Government and Department of Defense. She explains that the "clinical trials" or "approval" are not applicable regulatory frameworks in case of the covid-19 injection "countermeasures". Katherine has created a website as a resource for idividual citizens who want to file complaints or lawsuits on their own called "Five Small Stones"" https://5smallstones.com/write-a-letter/ More information on Katherine's work can be found using these links: https://bailiwicknewsarchives.files.wordpress.com/2022/10/2022.09.20-american-domestic-bioterrorism-program-large-print.pdf The other shortest versions: https://bailiwicknews.substack.com/p/prep-notes-for-an-interview https://bailiwicknews.substack.com/p/covid-19-injectable-bioweapons-as https://bailiwicknews.substack.com/p/distillation

Alexandra Latypova ("Sasha") is a retired pharmaceutical industry executive and entrepreneur. She holds an MBA degree from Dartmouth College and spent approximately 25 years in pharmaceutical research and development. Sasha later co-founded several clinical research organizations working as a contractor for about 60 pharmaceutical companies worldwide and was involved in the design, execution, data collection, analysis and submission of data to the FDA on hundreds of clinical trials. She also interacted with the FDA as part of the scientific consortium that developed new guidance for cardiovascular safety assessments of drugs and worked in all therapeutic areas and in many countries. Sasha currently holds board positions with several medical device and health care companies and volunteers for community and charitable organizations. You can follow Sasha on Bitchute here: https://www.bitchute.com/channel/7dNrFbLeGSev/

Join The Conversation! | https://trialsitenews.com/ We present the first part of an in-depth discussion between Robert Malone, an inventor of mRNA technology and vaccine expert, and Andrew Huff, a former EcoHealth Alliance vice president of data and technology and whistleblower. EcoHealth is an American research organization that allegedly sponsored gain-of-function experiments on bat coronaviruses at China’s Wuhan Institute of Virology and which is at the center of the so-called “lab leak theory” that SARS-CoV-2 is a man-made agent. Earlier this month Huff spoke to TrialSite News and Malone about whistleblower allegations he submitted to Congress earlier this month. Link | https://trialsitenews.com/wp-content/uploads/2022/02/Registered-mail-letter.docx In their exploration of EcoHealth and its operations, Huff and Malone discuss the overlap between biosurveillance, United States intelligence operations and bioweapons research. They also explore the perverse incentives that have made risky gain-of-function research almost commonplace among high-level virologists such as those engaged in coronavirus research at EcoHealth, the Wuhan lab and other researchers supported by the National Institutes of Health, the Centers for Disease Control, the Department of Defense and the U.S. State Department. Also, please review TrialSite’s previous articles about gain-of-function Link | https://trialsitenews.com/new-disclosures-support-lab-leak-theory-as-fauci-defends-covid-response-before-senate/ And Andrew Huff Link | https://trialsitenews.com/former-senior-executive-says-ecohealth-approached-by-cia/

The Therapeutic Goods Administration (TGA), Australia’s regulatory agency over drugs and related medicinal products, announced the lifting of its COVID-19 emergency-era ivermectin-restricted access by June 2023. TrialSite News chronicled early in the pandemic the build-up to the point in Australia when the TGA issued severe constraints on ivermectin. The publicly disclosed concern related to safety concerns for consumers using the drug without advice from licensed doctors as well as shortages. By September 2021, TGA banned general practitioner use of ivermectin. However, starting June 1, 2023, GPs prescribing oral ivermectin for ‘off-label’ uses will no longer be limited to specialists such as dermatologists, gastroenterologists and infectious diseases specialists. ------------------------------------ Join The Conversation! | https://trialsitenews.com/