"None of what Hilary Marston is doing is about practice of medicine. It's all about the globalist objectives, subverting public health for purposes of extracting wealth & controlling the population." https://flashlightsproductions.substack.com/p/from-preparedness-to-deadly-response?utm_source=youtube This is the second part of my VRBPAC Series with Sasha Latypova. We dissect the 400 page long transcript of the pivotal VRBPAC meeting on October 22, 2020. Its purpose was to prepare VRBPAC members and also the public for the coming Emergency Use Authorization of the Covid-19 mRNA shots. The VRBPAC is the FDA's external expert advisory committee that reviews data on vaccines and makes non‑binding recommendations to the agency on their safety, effectiveness, and appropriate use. To watch or listen to the first part, go here: https://flashlightsproductions.substack.com/p/the-fda-meeting-that-paved-the-way The meeting on October 22, 2020 is highly incriminatory. If any of these high FDA, CDC, NIH, NIAID and BARDA officials who gave presentations that day are ever being held accountable, there is a wealth of incriminating data in their many presentations. Ten health agency employees gave slide show presentations during the meeting. Many of them were long and dense. Since it was a public meeting, all the meeting material is public as well. You can access everything here: https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-october-22-2020-meeting-announcement#event-materials High FDA, CDC, NIH, NIAID, BARDA Officials Must Be Held Accountable for Covid Crimes The Covid clinical trials were as fake and barbaric as everything else that had to do with the so-called Pandemic. Those in high positions inside federal health agencies who lied to the public about the safety of the trials should be prosecuted for their lies that had deadly consequences. The Covid Clinical Trials Were a Charade to Mislead the Public: The Pre-Manufacturing of 30 Million Doses Proves It Approximately 30 million doses were manufactured starting July 2020 — before Phase 3 enrollment concluded and months before any data was reviewed. Which means that there was no safety evidence for the shots. Sasha Latypova said during the interview: "The first batches that were released onto the public in December were manufactured starting in July of 2020 - so before the phase three trials even enrolled. "When enrollment in phase three trials was completed in September, they had pre-manufactured about 30 million doses already. It was already sitting in the warehouse. By the time even the first set of data was reviewed by FDA on December 10th. All those vials were sitting already ready to go. "None of those 30 doses were dependent on any data, not animal, not human, no data of any kind. They were just pre-manufactured and then shipped disregarding anything. "And that is a major crime according to the current Food and Drugs and Cosmetics Act and the Public Health Services Act that governs biologics and biologic drugs. "But you see when the government declares an emergency, this major crime becomes an accomplishment, an achievement, something for which we get awards from President Trump and Biden and everyone. "This is how this crime cartel operates. They make totally illegal stuff legal when they say so. And then they profit massively of total knowledge, coordination, pre-planning, funding their own activities, putting all their secret Politburo members on this Data and Safety Monitoring Board and monitoring everything themselves." Hillary Marston, Fauci's Mentee You probably never heard about Dr. Hilary Marston but you should know who she is. In a just world, she would be prosecuted for participation in Covid crimes. Hilary Marston was one of the mentees of Anthony Fauci. Her career got a big boost shortly after her presentation at the October 2020 VRBPAC meeting: in January of 2021 she official switched over into an intelligence role as the Director of Medical and Biodefense Preparedness at the National Security Council. On top of that, she was also appointed, a few months later, as Senior Policy Advisor for Global Covid Response at the White House. This almost certainly happened with the full support and likely the initiative of Anthony Fauci himself. With his mentee Marston firmly embedded on the intelligence side, he now had a reliable executioner in the White House and the National Security Council. CHAPTERS 05:00 Hilary Marston's Presentation: Claims of Safety Without Showing Data 14:25 Marion Gruber's Role, EUA Framing, and Career at FDA 25:11 Transition to Hilary Marston and Her Career Overview 30:32 From NIAID to National Security Council: Marston's Biodefense Role 33:09 Matthew Hepburn, DARPA, and the 60‑Day Vaccine Concept 34:34 NSC, Pandemic Policy, and Who Actually Drove COVID Decisions 36:20 Canal Row Advisors: Monetizing FDA and Regulatory Connections 41:44 Start of Marston's VRBPAC Talk: "Role of NIH in COVID‑19 Vaccines" 41:44 Part 1 – From Pandemic Preparedness to Response 50:25 65‑Day Path to Phase 1 and Rapid mRNA Manufacturing 52:31 Phase 1 Launch, Early Trials, and "Quite Safe, Well Tolerated" Claims 55:11 Part 2 – Evaluating Safety and Efficacy via Harmonized Trials 56:21 "Harmonization" of Clinical Trials and Centralized Control 1:02:12 Clinical Trial Networks, HIV Platforms, and DoD Involvement 1:06:02 NIH‑Controlled Labs, Assays, and Case Definitions 1:09:17 Distinguishing Infection vs Vaccination and Controlling Endpoints 1:10:46 DSMB Structure and NIH's "Independent" Safety Oversight 1:12:59 CoVPN Architecture: NIH, BARDA, DoD, and Pharma Sponsors 1:19:24 NIH at Every Level of Trial Governance and the Pfizer Footnote 1:26:04 Trial Design: Sample Sizes, Endpoints, and Efficacy Metrics 1:29:20 Relative vs Absolute Efficacy and Interpreting the 95 Percent Figure RESOURCES VRBPAC-10.22.20-Meeting-Draft-Agenda.pdf How the FDA Lied to the American People About Covid-19 'Clinical Trials' 2020.08.25-sadove-fda-cdc-regulatory-updates-use-of-mcms-table-p.-18.pdf Marion F. Gruber, Ph.D., MS | LinkedIn About IAVI - IAVI Hilary Marston | LinkedIn Hilary Marston, MD, MPH | Principal, Drug and Biological Therapies Our Services - Canal Row VRBPAC-10.22.20-Meeting-Presentation-COVID19-Vaccine-Development-NIH-Role.pdf Matthew Hepburn | LinkedIn
