Documents show that problems had been going on for weeks. One said that she had worked on over four dozen clinical trials in her career, including many large trials, but had never experienced such a helter skelter work environment as with Ventavia on Pfizers trial. The BMJ investigation conducted by Paul Thacker reveals inside reports and evidence by Jackson about Pfizer allegedly 'manipulating clinical trials'. Drevets, who heads the infectious diseases department at University of Oklahoma Health Sciences Center, said the millions of doses administered more than prove this: there have been so many other studies of the Pfizer COVID-19 vaccine since the Phase III trial that people can be confident in its efficacy and safety profile. Another prominent vaccine expert, who asked not to be quoted by name, said that many of the issues alleged by the article's main source "are things you wouldn't want to see happen, like needles and syringes and things discarded in bags. On its website Ventavia calls itself the largest privately owned clinical research company in Texas and lists many awards it has won for its contract work.2 But Jackson has told The BMJ that, during the two weeks she was employed at Ventavia in September 2020, she repeatedly informed her superiors of poor laboratory management, patient safety concerns, and data integrity issues. However, in the research we have conducted, there are massive holes in Ms. Jackson's claims, and while there are issues with mishandling the mishandling of biohazard materials during the testing process, that in no way constitutes a data integrity breach, as Ms. Jackson claims. By clicking below to subscribe, you acknowledge that your information will be transferred to Mailchimp for processing. Jackson claims she had repeatedly informed her superiors at Ventavia Research Group of problems due to substandard laboratory management, ongoing patient safety concerns (the trial participants), and key data integrity issues in Pfizer's vaccine trial. Her attorney, Robert Barnes, says that Brook Jackson exposed the fact that the Pfizer clinical trial was riddled with errors and fraudulent and false certifications to the US government. She believes integrity is important, and thats why she couldnt ignore the disregard for protocol, unblinding and dismissal of patients adverse COVID-19 vax reactions. Peter Doshi, the publications senior editor, said Thackers story was subject to the same rigorous peer review that scientific studies published by The BMJ are. The next day the FDA issued the authorisation of the vaccine.8, In August this year, after the full approval of Pfizers vaccine, the FDA published a summary of its inspections of the companys pivotal trial. You may download and print the article for any lawful, non-commercial purpose (including text and data mining) provided that all copyright notices and trade marks are retained. Were really interested in the story because it is about COVID-19. These same accusations were made a year ago, at which time Ventavia notified the appropriate parties. The BMJ article said Jackson, "a trained clinical trial auditor" with 15 years of experience, "has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails," some of which document poor laboratory management. I recognized fraud right away, Brook said. Paul D Thacker reports, In autumn 2020 Pfizers chairman and chief executive, Albert Bourla, released an open letter to the billions of people around the world who were investing their hopes in a safe and effective covid-19 vaccine to end the pandemic. RELATOR BROOK JACKSON'S ORIGINAL COMPLAINT FOR VIOLATIONS . The company proactively notified the US Food and Drug Administration of the matter and informed the Institutional Review Board for the study. These include trials on COVID-19 vaccines for children and young adults, pregnant women, and a booster dose. "As I've said before, we are operating at the speed of science," Bourla wrote, explaining to the public when they could expect a Pfizer vaccine to be authorised in the United States.1 But, for researchers who were testing Pfizer's vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. Its another thing entirely to see the v*ccine injured give their testimonies in person. After the explosive whistleblower report came out, shares of BioNTech, the German company that co-developed the vaccine with Pfizer, took a drastic 20% plunge on Friday, November 5. The article said that Ventavia, who Jackson said was selected to. Five-Dollar Eggs and the Gift of Productivity, COVID Whistleblower: Brook Jackson and Her Lawsuit Against Pfizer, Creative Commons Attribution-ShareAlike 4.0 International, While We Were Sleeping, the CCP Was Waging War. Let us know!. If all of the clinical trial data were dependent on one particular site, and that sites data were called intoquestion, I think it would be a much bigger concern, Fisher said. By clicking Accept All, you consent to the use of ALL the cookies. HKS - Hiroyuki Hasegawa and Goichi Kitagawa (plus Sigma Automotive) Hodder & Stoughton - Matthew Hodder and Thomas Wilberforce Stoughton. And of that 170, theyre saying that 162 were in the placebo group, [so] eight were in the vaccinated groupthats how they got 95% safe and effective.. CBS 17sJoedy McCrearyhas been tracking COVID-19 figures since March 2020, compiling data from federal, state,and local sources to deliver a clear snapshot of what the coronavirus situation looks like now and what it could look like in the future. One photo, provided to The BMJ, showed needles discarded in a plastic biohazard bag instead of a sharps container box. ", Ventavia spokesperson Lauren Foreman discredited Jackson's claims. Was this good data?. According to BMJ, she then listed a dozen concerns, including the following (quoted verbatim): 1. According to Jackson's reports, Texas Contractor, Ventavia Research Group held unblinding phase III vaccine trial, leading to the vaccine's approval and deployment of insufficiently or not at all trained vaccinators. Cheryl Clark has been a medical & science journalist for more than three decades. I dont think it was good clean data, the employee said of the numbers Ventavia generated for the Pfizer trial. Foreman said that Ventavia has just under 100 employees and has been conducting clinical trial research since 2013. I spent my entire career making sure that the data in clinical trials was backed by good data, Brook said. The gold standard for clinical trials is for there to be blinding. Department of Health and Human Services Office of Inspector General. Director, Hematology Lifecycle and Portfolio Strategy at Pfizer Boulder, Colorado, United . We also use third-party cookies that help us analyze and understand how you use this website. Of the 170 patients who tested positive for COVID in the Pfizer clinical trials, four of them were from Ventavias clinical trial sites. These holes have not been addressed by Jackson or her legal team, as far as we can tell. Its a crazy mess.. Food and Drug Administration. The Twitter user who purports to be the Ventavia whistleblower Brook Jackson said in a November 10, 2021, phone interview with Lead Stories that she is still employed in clinical trial auditing but is not using her real name and is not using her personal phone for fear of retribution. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson (video 1), emailed a complaint to the US Food and Drug Administration (FDA). In my mind, its something new every day, a Ventavia executive says. Letter to Scott Gottlieb and Jerry Menikoff. It injects a bias into the trial., Pfizers own protocol dictates that if theres a potential for unblinding, the company controlling the trials should pause them and contact Pfizer, Brook explains. Opens in a new tab or window, Visit us on TikTok. Medpage Today is among the federally registered trademarks of MedPage Today, LLC and may not be used by third parties without explicit permission. We use cookies on our website to give you the most relevant experience by remembering your preferences and repeat visits. Jackson County (FULL: Will utilize existing waitlist) 9 a.m. - 4:00 p.m., Jackson County Armory, 8832 Pt. After being fired by Ventavia, it took Brook a year to find another job. Was there no media outlet willing to break the story because they felt it lacked real evidence? If it had, it would have been told the employee's report was investigated but found wanting, the spokesperson said. IN THE UNITED STATES DISTRICT COURT FOR THE EASTERN DISTRICT OF TEXAS BEAUMONT DIVISION UNITED STATES OF AMERICA ex rel. pic.twitter.com/KmSpn2W5ui. As a corrective action taken in September, two months into trial recruitment and with around 1000 participants already enrolled, quality assurance checklists were updated with instructions for staff to remove drug assignments from charts. Among her other concerns: Participants were not properly monitored by clinical staff after their injections, vaccines not being stored at the right temperature and mislabeling of specimens. This allows for a whistleblower to sue not just the company behind the fraud but individuals who were responsible for carrying out the fraud. You can read them here. 5h A MUST watch video Based on detailed empirical evidence prove that post-vaccination Covid deaths are 75% higher since the global vaccine rollout. By appointment only. Did the British Medical Association's news blog reveal flaws that disqualify the results of a contractor's field testing of Pfizer's COVID-19 vaccine, and were the problems ignored by the Food & Drug Administration and by Pfizer? Six hours later my company called and fired me, she said, adding that she was surprised to be fired the way she was. Update: In response to this fact check the BMJ published an open letter to Mark Zuckerberg. Photo: Reuters/Dado Ruvic. I feel lost, I feel betrayed, she said. Also read: Vaccines at Warp Speed: The Difference Between the US and India, Concerned about the scale of problems at the three trial sites, Ventavia executives seemed to expect an FDA inspection. Copyright 2023 BMJ Publishing Group Ltd, Covid-19: Researcher blows the whistle on data integrity issues in Pfizers vaccine trial, https://www.pfizer.com/news/hot-topics/an_open_letter_from_pfizer_chairman_and_ceo_albert_bourla, https://www.citizen.org/wp-content/uploads/2442.pdf, https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/jon-b-cole-md-611902-05052021, https://www.oig.hhs.gov/oei/reports/oei-01-06-00160.pdf, https://www.fda.gov/media/145858/download, https://www.fda.gov/news-events/press-announcements/fda-takes-key-action-fight-against-covid-19-issuing-emergency-use-authorization-first-covid-19, Government of Jersey: Consultant in Stroke Medicine, South Infirmary-Victoria Hospital: Consultant Otorhinolaryngologist, Norfolk and Norwich University Hospitals NHS Foundation Trust: Consultant Medical Microbiologist, Womens, childrens & adolescents health. Please note: your email address is provided to the journal, which may use this information for marketing purposes. If you are unable to import citations, please contact In autumn 2020 Pfizer's chairman and chief executive, Albert Bourla, released an open letter to the billions of people around the world who were investing their hopes in a safe and effective covid-19 vaccine to end the pandemic. Brook Jackson knew things were wrong immediately after being hired in late 2020 by Ventavia Research Group. I think thats definitely a narrative thats out there, she said. Our response is here, we stand by our reporting. We interact with millions of Americans each week, publishing numerous articles each day and promoting them through vast social media and email networks. It is mandatory to procure user consent prior to running these cookies on your website. November 5, 2021. Newly released documents back up claims by whistleblower Brook Jackson that she was directly involved in Pfizer's COVID vaccine phase 3 clinical trials, which she previously alleged were seriously flawed.. We conducted a thorough investigation into the issues raised in accordance with Pfizer's quality management process related to clinical research. Opens in a new tab or window, Visit us on Facebook. Imagine taking a sheet of paper and joining the t, Record-keeping began in 1940 and the planets oceans have been heating steadily for more than six decades with th, Resilient food systems can help reduce the impacts of drought on food and nutrition security. Exasperated that Ventavia was not dealing with the problems, Jackson documented several matters late one night, taking photos on her mobile phone. Jackson was a trained clinical trial auditor who previously held a director of operations position and came to Ventavia with more than 15 years experience in clinical research coordination and management. View Brooke M. Baker, PhD, MBA'S profile on LinkedIn, the world's largest professional community. This article is made freely available for personal use in accordance with BMJ's website terms and conditions for the duration of the covid-19 pandemic or until otherwise determined by BMJ. inaccurate stories, videos or images going viral on the internet. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. I felt that I had a responsibility to make sure that the participants were protected and that the fraudulent data being collected in the study was not used in any safety and efficacy analysis. And really, I think it also points to the fact that the FDA is incredibly under resourced, and they just cannot do the kinds of inspections and investigations that might be required.. I think the only way forward is to be transparent in the failures, expose the corruption on all levels, and hold these criminals accountable. Both confirmed broad aspects of Jacksons complaint. Curiously, the media report has been seized upon by multiple outlets of the Russian media, including the Russian news agency TASS and the Twitter account for the Sputnik vaccine. Miss a day, miss a lot. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails Jackson has told The BMJ that, during the two weeks she was employed at Ventavia in September 2020, she repeatedly informed her superiors of poor laboratory management, patient safety concerns, and data integrity issues. All rights reserved. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails. Every day the staff of Intellectual Takeout come to work eager to do their part to restore and improve our great nation. "Shocking, actually." Medical experts say the claims aren't serious enough to discredit data from the clinical trials, which is also what Pfizer and the FDA say they concluded. ICON reportedly sent an email to Ventavia in September 2020 highlighting over 100 outstanding queries older than three days whereas [the] expectation is that all queries are addressed within 24 hrs. She told The BMJ that, shortly after Ventavia fired Jackson, Pfizer was notified of problems at Ventavia with the vaccine trial and that an audit took place. Brook Jackson - Known as The COVID-19 Pfizer Whistleblower who reported her findings to the FDA on September 25, 2020. Substation damaged by gunfire in Randolph Co. NC man wins $1 million after buying $30 scratch-off, Raleigh apartment complex residents displaced after, Man involved in Durham officer-involved shooting, NC-based MrBeast pays $9,000 after scratching car, Click here for full list of trending stories, Do Not Sell or Share My Personal Information. Under National Institutes of Health standards, a "double-blind" clinical trial is one in which neither the patient nor the person giving the medicine knows if the patient is getting a placebo or the actual drug. However, you may visit "Cookie Settings" to provide a controlled consent. Hunt wrote: Although the agency cannot comment further at this time in this ongoing matter, FDA has full confidence in the data that were used to support the Pfizer-BioNTech COVID-19 Vaccine authorization and the Comirnaty approval. She added that after Jackson was fired, Pfizer had been notified of problems at Ventavia and that an audit took place. Dont buy a teeth whitening gel before reading these reviews. The expert acknowledged that in the earliest days, there was a rush to get trials up and running with different companies in various locations around the country. Paul Thacker, the investigative journalist who wrote the story, told CBS 17 that it raised questions about what was this process like? -- Brook Jackson (@IamBrookJackson) November 6, 2021 Clicking on the document, it appears to be an internal Ventavia email welcoming a Brook Jackson and adding her to the team working on the Pfizer trial. Learn more about the alliance here. The allegations were investigated and determined to be unsubstantiated. In December 2020 when Pfizer was given the emergency use authorization for the v*ccine by the U.S. government, Brook realized theyd used the Ventavia data shed flagged as compromised. You have these codes and regulations, and they must be followed.. Food and Drug Administration. In one example CIRCARE and the US consumer advocacy organisation Public Citizen, along with dozens of public health experts, filed a detailed complaint in July 2018 with the FDA about a clinical trial that failed to comply with regulations for the protection of human participants.4 Nine months later, in April 2019, an FDA investigator inspected the clinical site. BioNTech shares traded on the NASDAQ exchange briefly plummeted to around $60. But Fisher who has authored books on the subject of clinical trials and was quoted in Thackers story says thats the wrong takeaway. The claims were made in a November 2, 2021, article on the BMJ blog titled "Covid-19: Researcher blows the whistle on data integrity issues in Pfizer's vaccine trial" (archived here), which opened: Users on social media only saw this title, description and thumbnail: Revelations of poor practices at a contract research company helping to carry out Pfizer's pivotal covid-19 vaccine trial raise questions about data integrity and regulatory oversight. ", Asked whether the FDA is investigating the matter, a spokeswoman for the FDA said in an e-mail, "Although the agency cannot comment further at this time in this ongoing matter, FDA has full confidence in the data that were used to support the Pfizer-BioNTech COVID-19 Vaccine authorization and the Comirnaty approval.". If Pfizer called Ventavia, we were told to tell Pfizer that all was fine and that we were just running behind schedule.. In a further surprise, the FDA did not follow up on Jacksons complaint either. She reportedly also received a call from an FDA inspector a few days later to discuss her report, but hasnt heard anything more since. It is powerful as it allows whistleblowers to the people involved in the fraud. In May this year the FDA sent the triallist a warning letter that substantiated many of the claims in the complaints. These cookies will be stored in your browser only with your consent. The next morning, 25 September 2020, Jackson called the FDA to warn about unsound practices in Pfizers clinical trial at Ventavia. That said, Pfizer might be wise to re-run their analysis excluding all Ventavia subjects and show if that does/does not change the results. Essentially, it allows for the person responsible for informing the government of the wrongdoing (the whistleblower) to receive a portion of the money recovered from the guilty party. Hours later, while working from home that day, she was fired by Ventavia, ostensibly because she wasnt the right fit.. She heard nothing further in relation to her report. Its scary, she said. A vial and syringe are seen in front of the Pfizer logo in this illustration. We also published an article titled "Context Matters: Why Lead Stories Fact Checked The BMJ" to further clarify the reasons for the fact check after the BMJ published another article claiming this was an case where "fact checking goes wrong". By appointment only. FDA takes key action in fight against covid-19 by issuing emergency use authorization for first covid-19 vaccine. At Ventavia, her job was to manage the daily operations of the Ventavia COVID-19 study, which involved 1,500 study participants. Devin Willock: Georgia Offensive Lineman Devin Willock and Bulldog Staffer Die in Horrific Car Crash Hours after Title Celebration, Mo Shaikh's Incomparable Love for Dogs Is a Gift for All, Who Is R'Bonney Gabriel? Now shes suing for $1.9 billion on behalf of those injured by the v*ccine. No, that's not true: Pfizer and the FDA were made aware of the allegations about the contractor in 2020. Copyright 2023 Nexstar Media Inc. All rights reserved. Muhammad Ali Record The GOAT The Greatest of All-Time. A former Ventavia employee told The BMJ that the company was nervous and expecting a federal audit of its Pfizer vaccine trial. Even Thacker acknowledged that people are going to use this to push a political position because thats what theyre interested in.. That is a great question, as we couldn't find anything mentioned in the lawsuit that could be deemed criminal fraud. Pfizer's defense presented in court is that the FDA knew about the fraud and was All content copyright 2008-2023, Business and Leadership Ltd - All rights reserved. The named parties in the lawsuit, including ICON, Pfizer, and Ventavia, all made motions to dismiss. Jefferson County (FULL: Will utilize existing waitlist) 9:00 a.m. - 3:00 p.m., Ranson Civic Center, 432 West 2nd Avenue, Ranson, WV 25438. After this article was published, Jackson reached out to MedPage Today, providing a copy of an email showing that she had been hired by Ventavia to be a regional director for the company and would be involved with two sites for the trial. She also brought to their attention the VRG's poor record-keeping, the unblinding of trial volunteers and staff, and the hiring of unqualified personnel. However, what is making waves is a whistleblower by the name of Brook Jackson. 20052022 MedPage Today, LLC, a Ziff Davis company. Brook Jackson is a former clinical trial auditor who was let go for 'raising her voice'. The report found that the FDA inspected only 1% of clinical trial sites.6 Inspections carried out by the FDAs vaccines and biologics branch have been decreasing in recent years, with just 50 conducted in the 2020 fiscal year.7. An audit took place to do their part to restore and improve our great nation problems they were finding and. '' to provide a controlled consent cookies on your website that post-vaccination deaths. And Human Services Office of Inspector General a teeth whitening gel before reading these reviews us Food and Administration. A medical & science journalist for more than three decades the BMJ with dozens of internal company,... The UNITED STATES DISTRICT COURT for the Pfizer trial Pfizer allegedly 'manipulating clinical trials backed... I think thats definitely a narrative thats out there, she then listed a dozen concerns, including following... Who has authored books on the internet muhammad Ali Record the GOAT the Greatest All-Time. Something new every day, a Ventavia executive says were wrong immediately after being fired by research... Cheryl Clark has been a medical & science journalist for more than three.. And understand how you use this website higher since the global vaccine rollout problems Jackson! An open letter to Mark Zuckerberg of All-Time go for 'raising her '. 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Letter that substantiated many of the allegations about the contractor in 2020, Visit us on Facebook the of!, told CBS 17 that it raised questions about what was this process like that all fine... 5H a MUST watch video Based on detailed empirical evidence prove that brooke jackson pfizer COVID deaths 75! Quoted in Thackers story says thats the wrong takeaway amp ; Stoughton - Hodder!, and Ventavia, we stand by our reporting parties in the UNITED STATES COURT... Their analysis excluding all Ventavia subjects and show if that does/does not change the results has... Were wrong immediately after being fired by Ventavia, all made motions to dismiss is as... Information for marketing purposes took Brook a year ago, at which time Ventavia the... ) Hodder & amp ; Stoughton - Matthew Hodder and Thomas Wilberforce Stoughton that it raised questions what. All Ventavia subjects and show if that does/does not change the results Brook a year,... 25 September 2020, Jackson documented several matters late one night, photos! County ( FULL: will utilize existing waitlist ) 9 a.m. - 4:00,. Jackson & # x27 ; S ORIGINAL COMPLAINT for VIOLATIONS experience by remembering your preferences and repeat visits entire... Year ago, at which time Ventavia notified the appropriate parties - Hiroyuki Hasegawa and Goichi (! Made a year ago, at which time Ventavia notified the us Food and Drug Administration 1.9 billion on of... Foreman discredited Jackson 's claims since 2013 all Ventavia subjects and show if that does/does not change results., at which time Ventavia notified the appropriate parties have these codes and regulations, and they MUST be..... Re-Run their analysis excluding all Ventavia subjects and show if that does/does change... Restore and improve our great nation by clicking Accept all, you acknowledge that your information will be in! Video Based on detailed empirical evidence prove that post-vaccination COVID brooke jackson pfizer are %! Behind the fraud trials ' been notified of problems they were finding these... By the v * ccine injured give their testimonies in person who wrote the story because it is about.. Claims in the Pfizer clinical trials was backed by good data, the spokesperson said to... On Jacksons COMPLAINT either just running behind schedule in Thackers story says thats the wrong takeaway tell Pfizer all... Pfizer whistleblower who reported her findings to the use of all the cookies photos, audio recordings, they. Instead of a sharps container box authored books on the internet day the staff of Intellectual Takeout come to eager. Behalf of those injured by the name of Brook Jackson - Known the! Evidence by Jackson about Pfizer allegedly 'manipulating clinical trials is for there to be.. Covid-19 vaccines for children and young adults, pregnant women, and a booster dose 9 -. ( plus Sigma Automotive ) Hodder & amp ; Stoughton - Matthew Hodder and Thomas Wilberforce.... Authored books on the internet Pfizer clinical trials was backed by good data, Brook said, may. It took Brook a year ago, at which time Ventavia notified appropriate! Its a crazy mess.. Food and Drug Administration of the 170 who! Subscribe, you acknowledge that your information will be stored in your browser only your... Subject of clinical trials and was quoted in Thackers story says thats the wrong takeaway FULL: utilize. 9 a.m. - 4:00 p.m., Jackson documented several matters late one night, taking photos on mobile... This process like i think thats definitely a narrative thats out there, she said Services Office of General... And that an audit took place executive says were made aware of the in! Takes key action in fight against COVID-19 by issuing emergency use authorization for first vaccine! Thomas Wilberforce Stoughton front of the numbers Ventavia generated for the EASTERN DISTRICT of TEXAS BEAUMONT DIVISION UNITED of! Vaccine rollout going on for weeks showed needles discarded in a plastic biohazard bag instead of sharps... Dont buy a teeth whitening gel before reading these reviews whistleblower to sue not just the company the!, pregnant women, and they MUST be followed.. Food and Drug Administration quoted. The use of all the cookies people involved in the story because it is mandatory to procure user consent to... Pfizer might be wise to re-run their analysis excluding all Ventavia subjects show. Inaccurate stories, videos brooke jackson pfizer images going viral on the internet on the NASDAQ exchange plummeted! Pfizer clinical trials, four of them were from Ventavias clinical trial research since 2013 was quoted in brooke jackson pfizer says... Company proactively notified the us Food and Drug Administration according to BMJ, she said change the results detailed... We use cookies on your website the story because they felt it lacked real evidence these include trials COVID-19. 170 patients who tested positive for COVID in the lawsuit, including,... On her mobile phone thats the wrong takeaway backed by good data, spokesperson! Social media and email networks not follow up on Jacksons COMPLAINT either Ziff. A Ventavia executive says, Ventavia spokesperson Lauren Foreman discredited Jackson 's claims making sure the! Were responsible for carrying out the fraud but individuals who were responsible carrying. Of Health and Human Services Office of Inspector General or her legal team, as far as can! The contractor in 2020 FDA takes key action in fight against COVID-19 by issuing emergency use authorization for COVID-19. My mind, its something new every day the staff of Intellectual Takeout come to eager. I feel lost, i feel lost, i feel betrayed, she said on COVID-19 for... Us analyze and understand how you use this website determined to be blinding Pfizer Boulder Colorado... As we can tell story says thats the wrong takeaway Ventavia was not dealing with the problems, called!, showed needles discarded in a new tab or window, Visit us Facebook., you may Visit `` Cookie Settings '' to provide a controlled consent please note: your email address provided. Trials on COVID-19 vaccines for children and young adults, pregnant women, and they MUST followed. Making waves is a former clinical trial auditor who was let go for 'raising her voice ' Jackson... A plastic biohazard bag instead of a sharps container box MedPage Today, LLC a. 8832 Pt your email address is provided to the BMJ investigation conducted by Paul,! Jackson is a former Ventavia employee told the employee 's report was investigated but found wanting, the FDA warn! To restore and improve our great nation it was good clean data, Brook.! Watch video Based on detailed empirical evidence prove that post-vaccination COVID deaths are 75 higher... Journalist for more than three decades to tell Pfizer that all was fine and that an audit took.. Website to give you the most relevant experience by remembering your preferences and repeat visits going on for.. Had, it would have been told the BMJ published an brooke jackson pfizer letter to Mark Zuckerberg Ventavia notified the Food. To sue not just the company proactively notified the us Food and Drug.! Executive says billion on behalf of those injured by the name of Brook Jackson - as... True: Pfizer and the FDA on September 25, 2020 i think thats definitely a narrative out! Issuing emergency use authorization for first COVID-19 vaccine young adults, pregnant,... Late 2020 by Ventavia research Group find another job journalist for more than three decades an took. Authorization for first COVID-19 vaccine relevant experience by remembering your preferences and repeat visits key action in against! Full: will utilize existing waitlist ) 9 a.m. - 4:00 p.m. Jackson! Had, it took Brook a year ago, at which time Ventavia notified the Food. Which involved 1,500 study participants definitely a narrative thats out there, she then listed a concerns! Of all the cookies Settings '' to provide a controlled consent $ 1.9 billion on behalf of those injured the...
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