LEGAL.

Order today at http://www.1775coffee.com/BRAND - code BRAND to save 15% off your order Visit http://www.Pawsitive.com, grab a kit, and use code BRAND to save 15% ⏰ BE HERE AT 12PM EST / 5PM GMT ⏰ Today I’m talking to Aaron Siri, the attorney taking on Big Pharma and exposing the cracks in vaccine mandates and public health regulation. From forcing the CDC to release hidden data to challenging mandates all the way to the Supreme Court, Aaron’s work uncovers how profit-driven motives and regulatory conflicts of interest shape the public health narrative. We discuss the shocking lack of rigorous safety trials for vaccines, the immunity granted to pharmaceutical companies, and the contentious claims about vaccines and autism. Aaron pulls back the curtain on the systems that prioritize profits over transparency, raising urgent questions about science, power, and individual rights. It’s a bold, eye-opening conversation that can only be had on Rumble.

Award winning investigative journalist Sharyl Attkisson sits down with Clayton Morris to discuss her new book "Follow The Science: How Big Pharma Misleads, Obscures, and Prevails.

Who fact checks the fact checkers? Attorney Tom Renz refutes a recent AP "fact check" and alleges that the real "disinformation" is calling COVID mRNA shots "vaccines" instead of "gene therapy" – and says the FDA itself admits this in documents from 2020. ••「 CALL IN & LINKS: https://drdrew.com/4242024 」•• Sasha Latypova – a former pharmaceutical executive – returns to discuss why Dr. Drew continues to vaccinate elderly patients despite warning against mRNA use for younger people, resisting vaccine mandates, and fighting against lockdowns. Tom Renz is an attorney from Ohio conducting 'Lawfare for Freedom' by fighting corruption surrounding the COVID-19 pandemic at state and federal levels. Find out more at https://renz-law.com and follow him at https://x.com/RenzTom Sasha Latypova is a former pharmaceutical R&D executive with over 25 years of experience in clinical trials, clinical technologies, and regulatory approvals. She owned and managed several contract research organizations and worked for more than 60 pharma companies worldwide. She interacted with the FDA as part of a scientific industry consortium on improving cardiac safety assessments in clinical trials. Follow her at https://x.com/sasha_latypova and read more at https://sashalatypova.substack.com 「 SUPPORT OUR SPONSORS 」 Find out more about the brands that make this show possible and get special discounts on Dr. Drew's favorite products at https://drdrew.com/sponsors • PALEOVALLEY - "Paleovalley has a wide variety of extraordinary products that are both healthful and delicious,” says Dr. Drew. Get 15% off your first order at https://drdrew.com/paleovalley • COZY EARTH - Susan and Drew love Cozy Earth's sheets & clothing made with super-soft viscose from bamboo! Use code DREW to save up to 40% at https://drdrew.com/cozy • TRU NIAGEN - For almost a decade, Dr. Drew has been taking a healthy-aging supplement called Tru Niagen, which uses a patented form of Nicotinamide Riboside to boost NAD levels. Use code DREW for 20% off at https://drdrew.com/truniagen • GENUCEL - Using a proprietary base formulated by a pharmacist, Genucel skincare can dramatically improve the appearance of facial redness and under-eye puffiness. Get a discount with promo code DREW at https://genucel.com/drew • THE WELLNESS COMPANY - Counteract harmful spike proteins with TWC's Signature Series Spike Support Formula containing nattokinase and selenium. Learn more about TWC's supplements at https://twc.health/drew 「 GEAR 」 • NANLITE - Dr. Drew upgraded his studio with Nanlite: the best lighting for film, TV, and live streaming podcasts. Bring your vision to life at https://drdrew.com/nanlite 「 MEDICAL NOTE 」 The CDC states that vaccines are safe & effective. Portions of this program may examine countervailing views on medical issues. Always consult your physician before making health decisions. 「 AFFILIATES 」 Some of the links from this show are affiliate links, and as an Amazon Associate, we may earn an affiliate commission from qualifying purchases – at no cost to you. 「 ABOUT the SHOW 」 Ask Dr. Drew is produced by Kaleb Nation (https://kalebnation.com) and Susan Pinsky (https://x.com/firstladyoflove). This show is for entertainment or informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment. 「 ABOUT DR. DREW 」 Dr. Drew is a board-certified physician with over 35 years of national radio shows, NYT bestselling books, and countless TV shows bearing his name. He's known for Celebrity Rehab (VH1), Teen Mom OG (MTV), The Masked Singer (FOX), multiple hit podcasts, and the iconic Loveline radio show. Dr. Drew Pinsky received his undergraduate degree from Amherst College and his M.D. from the University of Southern California, School of Medicine. Read more at https://drdrew.com/about

- Save 15% off Liver Medic's Leaky Gut Repair using code 'peoplesvoice' - visit: https://livermedic.com/step/leakygutspecial/ -To sponsor this show, email: sponsor@thepeoplesvoice.tv - Visit https://thepeoplesvoice.tv/IPV6 to take back control of the Internet The Israel-Iran conflict is an “inside job” by the globalist elite who are working to ensure the conflict will light the fuse to ignite a “holy war” that will spiral out of control into World War Three and lay the groundwork for the elite to usher in the “one world government” of the New World Order. According to an insider, recent events in the middle east, including the Israel-Hamas war and now the conflict with Iran have been planned by the global elite and are now playing out to the letter – with the ultimate goal of shaping the world in their own image. But there is just one problem for the globalist elite and their plans to enslave the human race. Their plans rely on the people of the world remaining ignorant – and we are not going to let that happen.

Oklahoma state representatives and senators met with an expert panel and constituents who provided evidence for the need to open up investigations into the hospital protocols that were utilized during the Covid-19 pandemic that took the lives of many of our citizens. We are also asking for the removal of the gene therapy injections which are falsely advertised, unsafe, contaminated with DNA, causing lethal blood clots and harming reproduction. Follow us at MicMeow.com! You can also Follow Us at: https://blessednewstv.com/@Intentional https://rumble.com/c/c-1822277 https://www.youtube.com/channel/UCm-d4W6oUojoFioPhIRGIEQ https://www.facebook.com/TheConservativeContinuum https://substack.com/@micsmeow https://www.patreon.com/user?u=73931020 https://twitter.com/micmeowed https://truthsocial.com/@micmeow https://gettr.com/user/micmeow https://franksocial.com/profile/219775 https://gab.com/Mic_Meow https://www.brighteon.com/channels/intentional Please consider taking a moment to visit our affiliates: griddownchowdown.com (discount code "mic") for delicious beef products. drstellamd.com (discount code "mic") to keep your medicine cabinet stocked. sherwood.tv.com (discount code "mic") for all of your holistic care needs. lifewave.com/micmeow to rejuvenate you and revitalize your skin.

WHAT: Novel Coronavirus Southwestern Intergovernmental Committee WHEN: Friday March 15th, 2024 at 1:00pm ET WHERE: Arizona State Capitol Complex 1700 W Washington Street , Phoenix, AZ, 85007 + LIVE on CHD.TV AGENDA: Discussing COVID vaccination and hospital protocols as well as an FDA lawsuit involving doctors Mary Talley Bowder, Paul Marik and Robert Apter. Dr. Peter McCullough to join the hearing. https://az.childrenshealthdefense.org/events/novel-coronavirus-southwestern-intergovernmental-committee-part-3/ https://www.azleg.gov/icommittee/Novel%20Coronavirus%20Southwestern%20Intergovernmental%20Committee.pdf

Support the work of VSRF at https://VacSafety.org/donate Donations are tax deductible and we need your support to continue our work into 2024. Or to text-to-donate, text LIBERTY to 53555 On this Thursday’s VSRF LIVE, Steve will be hosting live from the Second Annual Covid Litigation Conference in Las Vegas, Nevada. The Covid Litigation Conference is the premier legal event where experienced lawyers in the Covid space come together to connect and to get educated about this burgeoning legal landscape. There are potentially MILLIONS of Covid litigation cases waiting to be brought forward involving the illegal Covid vaccine mandates and the wrongful terminations that occurred as a result of them across the US in 2021 and 2022. Steve will be interviewing some of the most recognized and experienced attorneys in the field currently, including Robert Barnes, Warner Mendenhall, Tricia Lindsey and many more. And wrongful termination lawsuits are just the tip of the iceberg when it comes to the myriad COVID related illegal and fraudulent activities we have all been subject to for nearly 4 years. This is surely the beginning of a massive wave of justice that will sweep over the US, ensuring our leaders know to never again attempt this kind of fraud and injustice on the American Public! Join us for this live discussion at the epicenter of a new era of justice and accountability in public health!

Sasha Latypova holds a graduate degree in business from Dartmouth College and is a retired pharmaceutical industry, research and development executive with 25 years of experience in conducting clinical trials. In this episode, we discuss the following: - Sasha did not work for a pharmaceutical company, she contracted to pharma companies. She conducted clinical trials in imaging, and later in cardiovascular safety monitoring. Most companies now outsource their clinical trials to contractors, like Sasha. So, Sasha was responsible for being in compliance to the regulators at all times, when conducting these trials. She is aware of all the regulations. - Sasha retired from her work in the pharmaceutical industry before the Covid19 period began. We discuss why she became interested in the Covid situation, both the early treatment and the new vaccines. - Sasha first became suspicious when the public health officials started to suppress hydroxychloroquine, as she had experience with this drug. They tried to smear this drug with cardiovascular arrythmia, which she was familiar with in her previous work. She knew for sure that hydroxychloroquine did not have that problem, especially when take for a short time frame, as it was for Covid. - She was the first to notice the batch variability of Covid vaccine adverse events in VAERS. Sasha collaborated with Craig Paardekooper on the website “How bad is my batch”. She knew right away that these products were not Good Manufacturing compliant. This was her conclusion by October 2021. She wrote letters to the CDC and FDA about this. Senator Johnson brought this data to the attention of the CDC and FDA also. The CDC and FDA never did anything. - At the end of 2021, Mike Yeadon sent Sasha a package of leaked documents from the EMA, about 800 pages worth, and a dozen emails between the regulators (EMA, MHRA, FDA). This package was actually leaked around Nov 30, 2020. It was clear from these documents, that this drug product was substandard, and the worse product she had ever seen. The bulk of the documents were from EMA regulators themselves. - Sasha tells us the number one thing that the regulators have to approve is the manufacturing. If you can’t manufacture, then safety and efficacy doesn’t matter. And yet all the scientists and doctors are focussing on safety and efficacy and no one is looking at manufacturing. The EMA documents showed evidence that the EMA regulators had raised 100 major objections to the approval of the Pfizer product. - An example of an objection. Pfizer had provided no evidence they were making the spike protein. And, we later learnt they faked the Western Blots, which was an assay to characterise the spike protein. It was a computer generated fake. - Sasha shows us the 3 drug approval pathways that are relevant to the approval of the vaccines in the USA. The normal FDA regulatory pathway for market approval. The Expanded Access Use pathway. The Emergency Use Authorisation pathway, and she explains the differences. There was a lot of confusion, and many people thought the Emergency Use Authorisation (EUA) was in fact the Expanded Use pathway, but they are very different. - The EUA comes under a brand new paragraph of the Food, Drug and Cosmetic Act, called Paragraph 564. EUA countermeasures can only be issued when the HHS has declared a public health emergency. And they are designated as non investigational. And so none of the laws that normally apply to drugs apply to these countermeasures. EG No IRB (investigational review board), no informed consent for recipients, and good manufacturing practise is not enforced. The only criteria needed, is that the HHS secretary thinks they may be effective. - For an in depth explanation of the legal framework, there is a good video of Sasha and Katherine Watt (the US para legal who worked with Sasha), explaining all the legal codes that were put in place in the USA, in the years preceding 2020. Sasha explains it took 3 years to unravel all the legal codes around this. See reference below. - Sasha shows us the transcript of a meeting, in which Doran Fink (deputy director of Vaccines and Related Biological Products Advisory Committee (VRBPAC) in the FDA, on Oct 22, 2020, stated that the FDA decided to use the EUA pathway rather then the expanded access use for approval of the Covid vaccines. And the reason was that expanded use required IRB and informed consent. That would add complexity. See Reference below. - Doran Fink is now at Moderna. - Sasha shows us the Pfizer timeline, showing the activity in terms of approvals etc from March 2020 through to Dec 2024. She points out that Doran Fink says they switched to EUA in Oct 2020, but she believes that in fact the switch happened in July 2020 as that is when Pfizer began mass producing the 30 million doses for the rollout. And, as we discuss, this was before phase 3 even started and before FDA approval of the product . That would have been illegal under IND. - In addition, the formula for the product was changed 5/6 times during the phase 3 trial ie they changed which drug they were testing. This was found in the 1100 page protocol document. - The FDA issued a BLA (Biologics License Application) in August 2021. So everyone thought the Pfizer vaccine was fully approved. But Sasha shows us the BLA letter, and it references the 2 Pfizer clinical trials, the Phase1/2 trial and the phase 3 trial, which were NOT clinical trials. So the BLA is fake, its illegal and the FDA is certifying the fraud. That’s why there are 2 products, but in the USA they never shipped the Comirnaty product , only the EUA product (Biontech). - Sasha explains that as long as the PREP Act is in place, these products “will not be deemed adulterated or misbranded”, and shows us the excerpt from the US code. This is why there is no enforcement of good manufacturing practise. - We discuss the involvement of the US Department of Defence. The DOD is the CEO of the operation , is totally in charge, and HHS has only an advisory role. The money all came from the DOD. - Sasha reveals that she has an audio of a discussion at a pharma company regarding a phone call that they received on Feb 4, 2020 from DOD. The DOD told them on that day, to switch from pan influenza (they were part of the P3 consortium) to Covid as Covid had been classified as a national security threat. See references. - What is the Pandemic Preparedness Program (P3), which was started in 2017. The person in charge of P3 is Colonel Matt Hepburn, and he is the mastermind. He has published TED talks on P3, and has claimed we can predict viruses and we will make vaccines in hours. - We ask Sasha who she thinks is behind the release of the virus and the injections. Websites referenced in the Interview; - Sasha Latypova’s Substack, which is called Due Diligence and Art. https://sashalatypova.substack.com - Video discussion between Katherine Watt and Sasha Latypova explaining the US Legal codes and the forensic work done by Katherine to uncover how the EUA was created. https://rumble.com/v3udbi4-sasha-latypova-and-katherine-watt-talking-about-non-regulation-of-non-medic.html -Doran Fink at VRBPAC meeting Oct 22, 2020. The entire transcript is here. Go to page 203 to see the answer by Doran Fink. https://www.fda.gov/media/143982/download - A good place for new readers to start. A summary of Everything - End 2023. https://sashalatypova.substack.com/p/summary-of-everything-and-quick-links - Audio Leak from pharma company regarding Feb 4, 2020 call from DOD. https://sashalatypova.substack.com/p/audio-leaked-from-astrazeneca-covid

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Covid-19 Vaccine Expert Panel Briefing to the Massachusetts Legislature and Public Health Officials