Corruption in Science News Stories

Excerpts of Key Corruption in Science News Stories in Major Media

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The Department of Justice secretly launched a grand jury investigation into a US nonprofit that steered American taxpayer funding to the Chinese lab suspected of leaking the COVID-19 virus and causing the global pandemic. Scientific experts and former federal officials have suggested that EcoHealth Alliance's grants to the China's Wuhan Institute of Virology (WIV) funded gain-of-function research that could have led to a lab leak – but records requests have repeatedly been blocked by the National Institutes of Health. The details of the apparent federal investigation of EcoHealth Alliance remain secret – and members of the House Select Subcommittee on the Coronavirus Pandemic, which released [a] 520-page report on the origins of and response to the pandemic, have declined to talk about it, citing concerns about interfering in any potential DOJ investigation. The National Institutes of Health (NIH), US Agency for International Development (USAID) and other agencies awarded millions of dollars' worth of grants to the now-suspended public health nonprofit – including a $4 million NIH project titled "Understanding the Risk of Bat Coronavirus Emergence." More than $1.4 million dollars flowed from NIH and USAID to the WIV for that project, which the agency's principal deputy director Dr. Lawrence Tabak later acknowledged was gain-of-function research on bat coronaviruses modified with SARS and MERS viruses to become 10,000 times more infectious.

Note: Read how the NIH bypassed the oversight process, allowing controversial gain-of-function experiments to proceed unchecked. Watch our Mindful News Brief on the strong evidence that bioweapons research created COVID-19. For more along these lines, read our concise summaries of news articles on COVID corruption and biotech dangers.

A final congressional report on COVID-19 released Monday has determined the virus likely emerged from a lab accident in China and that the U.S. government perpetrated "misinformation" by incorrectly calling the lab leak theory a "conspiracy." The House Oversight and Accountability Committee's COVID-19 panel, controlled by Republicans, issued its 520-page report two years after its investigation began. The report affirmed ... that a "lab-related incident" involving gain-of-function research in Wuhan is the most likely origin of the COVID-19 pandemic. The report specifically calls out Anthony Fauci ... saying that he pushed back on the lab leak theory and "prompted" a research report called "The Proximal Origin" that was used to discredit it. "Although Dr. Fauci believed the lab-leak theory to be a conspiracy theory at the start of the pandemic, it now appears that his position is that he does have an open mind about the origin of the virus–so long as it does not implicate EcoHealth Alliance, and by extension himself and NIAID. Understandably, as he signed off on the EcoHealth Alliance grant," the report stated. The massive report also examined the effectiveness and consequences of masks and mask mandates and stated that they were ineffective at controlling the spread of COVID-19. Prolonged lockdowns caused immeasurable harm to not only the American economy but also to the mental and physical health of Americans, with a particularly negative effect on younger citizens.

Note: Read how the NIH bypassed the oversight process, allowing controversial gain-of-function experiments to proceed unchecked. Watch our Mindful News Brief on the strong evidence that bioweapons research created COVID-19. For more along these lines, read our concise summaries of news articles on COVID corruption and biotech dangers.

The House Select Subcommittee on the Coronavirus Pandemic has released its final report, summarizing two years of investigations into the origins and handling of COVID-19. The 520-page report, published Monday, concludes that the virus most likely originated from a laboratory in Wuhan, China. The Republican-led committee cited biological characteristics of the virus and reports of illnesses among researchers at the Wuhan Institute of Virology in late 2019 as key evidence for its findings. The report also scrutinized the World Health Organization (WHO), accusing it of prioritizing the Chinese Communist Party's interests over its global mission to protect public health. The subcommittee criticized U.S. health officials and the Biden administration for what it described as overselling the effectiveness of vaccines in preventing transmission and infection. However, the report praised the early travel restrictions implemented by the Trump administration as a significant step in mitigating the pandemic's spread. This conclusion contrasts with other research pointing to the Huanan Seafood Market in Wuhan as the most likely origin of the virus. The WHO and many scientists have stated that the exact origins of the pandemic remain uncertain. The release of the report highlights the ongoing debate over the pandemic's beginnings and the global response, underscoring the complexities of managing an unprecedented public health crisis.

Note: Watch our Mindful News Brief on the strong evidence that bioweapons research created COVID-19. For more along these lines, read our concise summaries of news articles on COVID corruption and COVID vaccines.

Emails show Planned Parenthood negotiating terms regarding the donation of aborted fetuses for medical research. The emails discuss fetal tissue like any other commodity such as sugar or rice, nonchalantly negotiating for fetuses up to 23 weeks old from elective abortions. A heavily-redacted so-called "Research Plan" submitted to the University of California San Diego (UCSD) Institutional Review Board and approved in 2018 states scientists wanted 2,500 fetuses from up to almost the sixth month of gestation for experimentation. Although selling fetal tissue is illegal, donating it is not illegal. The contract between UCSD and Planned Parenthood appears to allow Planned Parenthood to retain "intellectual property rights relating to the" fetal tissue, although it also does not grant UCSD the independent right to "commercialize" the tissue. The emails were shared with The Post by [founder of Center for Medical Progress] David Daleiden. Daleiden ... accuses Planned Parenthood of racism. The English language consent forms contain 15 bullet points including language disclosing that the donated tissue may have "significant commercial value." However, that specific information is not included in the Spanish language consent forms which contain only 14 bullet points. "I don't understand why Planned Parenthood…. and UCSD felt that Spanish speaking mothers did not deserve to know that the body parts of their aborted children would be ‘commercialized" while English speaking mothers did deserve to have this fact disclosed to them," Daleiden [said]. The transfer of any aborted human fetal tissue for "valuable consideration" across state lines is a federal felony punishable by up to 10 years in prison or a fine of up to $500,000.

Note: Watch all the leaked footage of Planned Parenthood executives discussing the sale of aborted fetal tissue here. For more along these lines, read our concise summaries of news articles on corruption in science.

There's no question that activist David Daleiden surreptitiously recorded healthcare and biomedical services employees across the state of California with the intent of discrediting the healthcare provider, Planned Parenthood. It's against state law to record confidential conversations without the consent of all the parties involved. But that doesn't mean that California Atty. Gen. Xavier Becerra should have charged Daleiden and his co-conspirator, Susan Merritt, with 15 felony counts – one for each of the 14 people recorded, and a 15th for conspiracy. It's disturbingly aggressive for Becerra to apply this criminal statute to people who were trying to influence a contested issue of public policy. In similar cases, we have denounced moves to criminalize such behavior, especially in the case of animal welfare investigators who have gone undercover at slaughterhouses and other agricultural businesses to secretly record horrific and illegal abuses of animals. That work, too, is aimed at revealing wrongdoing and changing public policy. The videos ... were published online nearly two years ago by Daleiden's organization, the Center for Medical Progress. Officials of Planned Parenthood, whose staff members were seen on some of the recordings, denied any wrongdoing. Still, the online posting of the edited tapes triggered more than a dozen different state investigations ... and several now concluded congressional investigations into whether fetal tissue was being sold.

Note: Watch all the leaked footage of Planned Parenthood executives discussing the sale of aborted fetal tissue here. For more along these lines, read our concise summaries of news articles on corruption in science.

A former director at the tobacco giant Philip Morris International (PMI) was handed a role on an influential expert committee advising the UK government on cancer risks. Ruth Dempsey, the ex-director of scientific and regulatory affairs, spent 28 years at PMI before being appointed to the UK Committee on Carcinogenicity of Chemicals in Food, Consumer Products and the Environment (CoC). The committee's role is to provide ministers with independent advice. Yet since taking up the position in February 2020, Dempsey has continued to be paid by PMI for work including authoring a sponsored paper about regulatory strategies for heated tobacco products. She also owns shares in the tobacco giant ... and receives a PMI pension. But her appointment, unreported until now, raises questions about the potential for undue influence and possible access to inside information on policy and regulatory matters that may be valuable to the tobacco industry. PMI has a long history of lobbying and influence campaigns, including pushing against planned crackdowns on vaping. It has also invested heavily in promoting heated tobacco as an alternative to smoking and expects to ship around 140bn heated tobacco units in 2024, a 134% increase on its 59.7bn sales in 2019. Sophie Braznell, who monitors heated tobacco products as part of the University of Bath's Tobacco Control Research Group, said Dempsey's position on the committee risked undermining its work. "In permitting a former senior tobacco employee and consultant for the world's largest tobacco company to join this advisory committee, we jeopardise its objectivity and integrity."

Note: For more along these lines, see concise summaries of deeply revealing news articles on health and government corruption from reliable major media sources.

The tobacco company Philip Morris International has been accused of "manipulating science for profit" through funding research and advocacy work with scientists. Campaigners say that leaked documents from PMI and its Japanese affiliate also reveal plans to target politicians, doctors and the 2020 Tokyo Olympics as part of the multinational's marketing strategy to attract non-smokers to its heated tobacco product, IQOS. A paper from researchers at the Tobacco Control Research Group at the University of Bath said that Philip Morris Japan (PMJ), funded a Kyoto University study into smoking cessation via a third-party research organisation. The researchers said they could find no public record of PMJ's involvement, although a PMI spokesperson said its involvement had been attributed when the results were presented at a scientific conference in Greece in 2021. PMJ paid about Ł20,000 a month to FTI-Innovations, a life sciences consultancy run by a Tokyo University professor, for tasks such as promoting PMI's science and products at academic events. In one internal email, a PMJ employee claimed they had been told "to keep it a secret". Dr Sophie Braznell, one of [the paper's] authors, said: "The manipulation of science for profit harms us all, especially policymakers and consumers. It slows down and undermines public health policies, while encouraging the widespread use of harmful products."

Note: For more along these lines, see concise summaries of deeply revealing news articles on health and science corruption from reliable major media sources.

A small, tight-knit community of scientific sleuths has been unearthing growing evidence that many studies, including landmark papers published in top journals, contain manipulated images and falsified findings. These revelations have led to high-profile investigations, raised concerns about clinical trials, and culminated in the departure of university presidents. Their work – often posted on PubPeer, a website where users comment on published studies – has also forced a reckoning around how the crushing pressure to publish splashy results incentivizes fraud. "Claire Francis" is a pseudonym for someone who has commented on, by their own reckoning, 20,000 articles since 2010. About 2,000 of these studies were later retracted. Elisabeth Bik ... comments on papers using her real name, and she has earned a reputation for her preternatural ability to spot fishy figures. Bik has flagged issues with about 8,500 studies, contributing to 1,300 retractions and about 1,100 corrections, she told STAT. Those retractions include a study supporting a popular hypothesis for Alzheimer's disease that has been cited more than 2,000 times, as well as a stem cell paper cited nearly 4,500 times. Her work has made her the recipient of more derisive emails, cease-and-desist letters, and legal threats than Bik can count. That's not an uncommon experience, and Bik is an adviser to the Scientific Integrity Fund, which has set aside money to support sleuths being sued for their work.

Note: Top leaders in the field of medicine and science have spoken out about the rampant corruption and conflicts of interest in those industries. For more along these lines, explore concise summaries of revealing news articles on science corruption.

Anthony Fauci detailed how the research portfolio of his longtime former institute, the National Institute of Allergy and Infectious Diseases, did not distinguish between "biodefense efforts" and "naturally occurring" pathogens in a fall 2017 presentation. Fauci described "the joining with and ultimate indistinguishing of biodefense efforts and efforts directed at naturally occurring emerging and re-emerging infections. "Gain-of-function" research (GOF) makes viruses more pathogenic or transmissible. Much of this gain-of-function research is considered "dual use research of concern" (DURC) because it can be applied toward benevolent civilian aims or misapplied toward the development of bioweapons. Fauci's biodefense legacy has taken on a new significance in light of the COVID-19 pandemic. Critics, especially those who believe the pandemic is likely to have resulted from a lab accident, say the global proliferation of maximum security labs and GOF/DURC has made the world less safe. After the 2001 anthrax attacks, amid concerns about alleged "weapons of mass destruction," including biological weapons, former President George W. Bush asked Congress to invest billions in building maximum security labs capable of combating bioterrorism. By the late 2000s, fears of bioterrorism from the Middle East had faded. The Federal Bureau of Investigation's conclusion that a researcher at the U.S. Army Medical Research Institute on Infectious Diseases at Fort Detrick had been responsible for the 2001 anthrax attacks stoked a new kind of fear – of an expanding population of scientists with classified knowledge and access to pathogens. Counter-bioterrorism research at the National Institutes for Health surged from $53 million in 2001 to at least $1.6 billion in 2004. GAO reports uncovered major biosecurity breaches.

Note: Watch our Mindful News Brief on the strong evidence that bioweapons research created COVID-19. Meanwhile, Anthony Fauci admitted to congress that there was no scientific basis for many pandemic policies. Can anything he's said about gain-of-function research be trusted?

An influential doctor and advocate of adolescent gender treatments said she had not published a long-awaited study of puberty-blocking drugs because of the charged American political environment. The doctor, Johanna Olson-Kennedy, began the study in 2015 as part of a broader, multimillion-dollar federal project on transgender youth. She and colleagues recruited 95 children from across the country and gave them puberty blockers, which stave off the permanent physical changes – like breasts or a deepening voice – that could exacerbate their gender distress, known as dysphoria. The researchers followed the children for two years to see if the treatments improved their mental health. An older Dutch study had found that puberty blockers improved well-being, results that inspired clinics around the world to regularly prescribe the medications as part of what is now called gender-affirming care. But the American trial did not find a similar trend. Puberty blockers did not lead to mental health improvements, she said. In the nine years since the study was funded ... and as medical care for this small group of adolescents became a searing issue in American politics, Dr. Olson-Kennedy's team has not published the data. Asked why, she said the findings might fuel the kind of political attacks that have led to bans of the youth gender treatments in more than 20 states, one of which will soon be considered by the Supreme Court. "I do not want our work to be weaponized," she said.

Note: We believe that everyone has a right to exist and express themselves the way they want. Yet we value the health of all beings and the importance of informed choice when it comes to any potentially life-changing medical procedure. For more along these lines, explore summaries of revealing news articles on transgender medicine from reliable major media sources.

The Environmental Protection Agency's (EPA) internal watchdog has found that top agency officials retaliated against three staffers for expressing different scientific opinions. The employees who were victims of this alleged retaliation thought chemicals should be considered more toxic, while top officials sought to consider them safer, according to the reports from the EPA's inspector general. EPA scientist Sarah Gallagher says she thought the agency should consider the chemical as toxic to fetal development, while another official wanted to classify it as a lower-priority body weight issue. In another case documented in a report finding retaliation against scientist Martin Phillips, a senior science adviser allegedly changed an assessment in a way that removed "reproductive toxicity" as a concern from safety information that goes to people who work with the chemical. In a third report finding retaliation against scientist William Irwin, a manager also allegedly tried to remove evidence of reproductive toxicity. These instances appeared to have a chilling effect that could impact other agency scientists' willingness to stand up to management. "Other assessors noticed how those who disagreed with management were perceived," the reports said. They added that a person whose name was redacted testified that disagreeing or delaying the resolution of backlogged cases could cause management to label an employee "problematic."

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For nearly 40 years prior to the COVID-19 pandemic, [Anthony] Fauci had served as the ... director of the National Institute of Allergy and Infectious Diseases (NIAID), a subsidiary of the National Institutes of Health (NIH). Prior to COVID-19, Fauci had long supported funding pandemic research that other scientists found risky, if not downright dangerous. In 2014, there was a series of embarrassing safety lapses at U.S. government labs. In October 2014, President Barack Obama's administration paused federal funding of gain-of-function research that could make ... viruses transmissible via the respiratory route in mammals. In 2017, the White House produced the ... P3CO framework. Under P3CO, the NIH would forward grant proposals involving research on known pandemic pathogens or research that might create or enhance such pathogens to a new P3CO committee within HHS for a department-level risk-benefit analysis. To date, the P3CO committee has vetted just three research proposals involving so-called enhanced potential pandemic pathogens, out of potentially dozens that should have been examined. Fauci and NIH Director Francis Collins ... found a way to skirt the oversight process. They "realized that if they don't [forward proposals to HHS for review], there is no review." In 2014, [EcoHealth Alliance] received a five-year, $3.7 million NIAID grant to collect virus samples from human beings and bats in China and then experiment on these viruses at the Wuhan Institute of Virology. EcoHealth announced that it intended to create "chimeric" or hybrid viruses out of spike proteins, the part of a virus that allows it to enter and infect hosts cells, from SARS-like coronaviruses discovered in the wild and the backbone of another, already-known SARS virus. When EcoHealth's year five report was eventually submitted two years late, in 2021, it showed that additional chimeric viruses created in Wuhan demonstrated both enhanced transmission and lethality in humanized mice. By that time, the COVID-19 pandemic was already well underway.

Note: Don't miss our Mindful News Brief on the origins of COVID. For more along these lines, see concise summaries of deeply revealing news articles on COVID-19 and government corruption from reliable major media sources.

Nearly half of the AI-based medical devices approved by the US Food and Drug Administration (FDA) have not been trained on real patient data, according to a new study. The study, published in Nature Medicine, finds that 226 of the 521 devices authorised by the FDA lack published clinical validation data. "Although AI device manufacturers boast of the credibility of their technology with FDA authorisation, clearance does not mean that the devices have been properly evaluated for clinical effectiveness using real patient data," says first author Sammy Chouffani El Fassi. The US team of researchers examined the FDA's official "Artificial Intelligence and Machine Learning (AI/ML)-Enabled Medical Devices" database. "Using these hundreds of devices in this database, we wanted to determine what it really means for an AI medical device to be FDA-authorised," says Professor Gail Henderson, a researcher at the University of North Carolina's Department of Social Medicine. Of the 521 devices in this database, just 22 were validated using the "gold standard" – randomised controlled trials, while 43% (226) didn't have any published clinical validation. Some of these devices used "phantom images" instead – computer-generated images that didn't come from real patients. The rest of the devices used retrospective or prospective validation – tests based on patient data from the past or in real-time, respectively.

Note: For more along these lines, see concise summaries of deeply revealing news articles on health and artificial intelligence from reliable major media sources.

In December of 2002, Sharyl Attkisson, an Emmy-winning investigative reporter for CBS News, had an unsettling interview with smallpox expert Jonathan Tucker. In a post-9/11 world, with fears of terrorists using a long-eradicated disease like smallpox as a bioweapon, the US was preparing to bring back the smallpox inoculation program. But to Tucker, the very idea was "agonizing," writes Attkisson. Why? Because it involved "weighing the risk of a possible terrorist use of smallpox ... against the known risks of the vaccine," Tucker told the author. "A ‘toxic' vaccine?" She writes. "Didn't the smallpox vaccine save the world?" But as she soon discovered, it had serious side effects, including a surprisingly high possibility of death. Attkisson witnessed firsthand how deadly the vaccine could be in April of 2003, when a colleague at NBC, journalist David Bloom, died from deep vein thrombosis while on assignment in Iraq. He'd also recently been vaccinated for smallpox, and ... thrombosis was a possible side effect of the inoculation. The majority of scientific studies are funded and even dictated by drug companies. "Studies that could stand to truly solve our most consequential health problems aren't done if they don't ultimately advance a profitable pill or injection," Attkisson writes. "These aren't necessarily drugs designed to make us well, but ones we'll ‘need' for life," writes Attkisson. Some [drug companies] hire "ghostwriters" to author studies promoting a new drug, exaggerating benefits and downplaying risks, and then paying a doctor or medical expert to sign their name to it. "We exist largely in an artificial reality brought to you by the makers of the latest pill or injection," she writes. "It's a reality where invisible forces work daily to hype fears about certain illnesses, and exaggerate the supposed benefits of treatments and cures."

Note: Top leaders in the field of medicine and science have spoken out about the rampant corruption and conflicts of interest in those industries. For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption from reliable major media sources.

[Don] Poldermans was a prolific medical researcher at Erasmus Medical Center in the Netherlands, where he analyzed the standards of care for cardiac events after surgery, publishing a series of definitive studies from 1999 until the early 2010s. One crucial question he studied: Should you give patients a beta blocker, which lowers blood pressure, before certain surgeries? Poldermans's research said yes. European medical guidelines (and to a lesser extent US guidelines) recommended it accordingly. The problem? Poldermans's data was reportedly fake. A 2012 inquiry by Erasmus Medical School, his employer, into allegations of misconduct found that he "used patient data without written permission, used fictitious data and ... submitted to conferences [reports] which included knowingly unreliable data." Poldermans admitted the allegations and apologized. After the revelations, a new meta-analysis was published in 2014, evaluating whether to use beta blockers before non-cardiac surgery. It found that a course of beta blockers made it 27 percent more likely that someone would die within 30 days of their surgery. Millions of surgeries were conducted across the US and Europe during the years from 2009 to 2013 when those misguided guidelines were in place. One provocative analysis ... estimated that there were 800,000 deaths compared to if the best practices had been established five years sooner.

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Although seemingly noble, the billions pumped into the US government's National Science Foundation don't always translate into finding cures for debilitating diseases, or developing groundbreaking technologies. In recent years, although technology and peer-review techniques have become more widespread, fraud has remained a consistent issue. As [J.B.] Carlisle analyzed dozens of government-funded control trials, he found a staggering 44% contained false data. These findings are swept under the rug by most mainstream news outlets. There are several ways the government introduces bias into research. For one, the state often ignores certain scientific queries, forcing researchers to adopt different hypotheses or study different questions to gain any funding. Without any market forces guiding research and development, study objectives start aligning more with the interests of bureaucrats and less with the interests of patients. Government agencies also don't want to fund proposals that contradict the agency's political ideas. If the research's outcome even slightly threatens the government's power, funding is likely to be cut off, often for extended periods. These outcomes are clearest when it comes to funding regarding the social sciences and economics. 34% percent of scientists receiving federal funding have acknowledged engaging in research misconduct to align research with their funder's political and economic agenda.

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Late last year, the U.S. Food and Drug Administration (FDA) quietly introduced a regulation that may be one of the most important shifts in how [clinical research organizations, universities large and small, pharma companies, and multi-billion dollar corporations] conduct future medical and public health research. A bedrock of ethical research design is the universal requirement of informed consent for any medical procedure, treatment, or intervention. These measures have generally been strengthened since the Nuremberg Trials, formally adopted across the U.S. government through the institutional review board (IRB) system. An IRB is a committee of specialists and administrators at each institution that oversees research design and assures the protection of research subjects. At its core, the new FDA rule change allows any IRB to broadly assume the FDA's own exemption power, dubiously granted under the 21st Century Cures Act of 2016, to grant exemptions to informed consent requirements based on "minimal risk." Based on vague guidelines, it effectively gives thousands of IRB committees the unilateral ability to determine that researchers need not obtain true informed consent from research participants. The relaxed standards could facilitate the quick approval of controversial research projects. The Gates Foundation-backed Oxitec program is currently releasing millions of genetically modified mosquitos in the Florida Keys. Another application of the relaxed standards is to government-funded studies of online posts designed to identify "misinformation." Entities like the Stanford Internet Observatory have laundered government demands for censorship of speech–even true speech–in online settings like Facebook and X (formerly Twitter). The literal purpose of this research is to harm its research subjects by censoring their speech and labeling them as purveyors of misinformation. In 2021, a conservative journalist sued Stanford University for slandering him via this research project, which never sought his informed consent to be a subject of their study. Under the new FDA rule, IRBs everywhere would feel no compunction to require it.

Note: Read about the shocking history of human experimentation. See a disturbing timeline of corporate and government experiments that treated people like guinea pigs. For more, see concise summaries of deeply revealing news articles on corruption in science from reliable major media sources.

A recent audit of Pentagon funding of gain-of-function research outside the US "may have shielded" collaborations with Chinese biotech firms – including at least one linked to Beijing's military, a Republican senator alleged. Sen. Roger Marshall (R-Kan.) pressed Defense Secretary Lloyd Austin for answers about redactions that had concealed the firms – WuXi AppTec, Pharmaron Beijing Co., and Genscript Inc. – from public scrutiny in the audit, according to a letter. "American taxpayers deserve transparency about the programs they are funding, and I am disappointed this OIG report does not provide that accountability," Marshall wrote. According to the Defense Department Office of Inspector General audit, more than $15.5 million in grants between 2014 and 2023 flowed through subrecipients to "contracting research organization[s] in China or other foreign countries for research related to potential enhancement of pathogens of pandemic potential." However, the 20-page audit cited "significant limitations with the adequacy of data" – and said the Pentagon "did not track funding at the level of detail necessary to determine whether the DoD provided funding ... for the gain-of-function experiments. Such research is classified as "offensive biological work" by the Pentagon, which Marshall said "raises questions" about National Institutes of Health (NIH) officials having admitted this year to funding gain-of-function experiments at the ... Wuhan Institute of Virology.

Note: Watch our 15-min Mindful News Brief video on the strong evidence that bioweapons research created COVID-19. For more along these lines, see concise summaries of deeply revealing news articles on COVID-19 and military corruption from reliable major media sources.

The year before the outbreak, the Wuhan institute, working with U.S. partners, had proposed creating viruses with SARS-CoV-2's defining feature. Much of this work was conducted in partnership with the EcoHealth Alliance, a U.S.-based scientific organization that, since 2002, has been awarded over $80 million in federal funding to research the risks of emerging infectious diseases. The laboratory pursued risky research that resulted in viruses becoming more infectious: Coronaviruses were grown from samples from infected animals and genetically reconstructed and recombined to create new viruses unknown in nature. In 2021, The Intercept published a leaked 2018 grant proposal for a research project named Defuse, which had been written as a collaboration between EcoHealth, the Wuhan institute and Ralph Baric at the University of North Carolina. The Defuse project proposed to search for and create SARS-like viruses carrying spikes with a unique feature: a furin cleavage site – the same feature that enhances infectiousness in humans, making it capable of causing a pandemic. As the pandemic raged, their American collaborators failed to publicly reveal the existence of the Defuse proposal. One alarming detail – leaked to The Wall Street Journal and confirmed by current and former U.S. government officials – is that scientists ... fell ill with Covid-like symptoms in the fall of 2019. One of the scientists had been named in the Defuse proposal as the person in charge of virus discovery work. [This] would be the most costly accident in the history of science. U.S. federal funding helped to build an unprecedented collection of SARS-like viruses at the Wuhan institute, as well as contributing to research that enhanced them.

Note: Watch our 15-min Mindful News Brief video for a deeper dive into the strong evidence that bioweapons research created COVID-19. For more along these lines, see concise summaries of deeply revealing news articles on COVID and government corruption from reliable major media sources.

For nearly nine years Anthony Fauci's institute concealed plans to engineer a pandemic capable mpox virus with a case fatality rate of up to 15 percent, congressional investigators revealed in a new report. In June 2015, a scientist at the National Institute of Allergy and Infectious Diseases received formal approval from the National Institutes of Health's Institutional Review Board for experiments expected to engineer an mpox virus with high transmissibility and moderate mortality. NIAID – the institute Fauci oversaw for nearly four decades and which underwrites most federally funded gain-of-function research – concealed the project's approval from investigators with the House Committee on Energy and Commerce over the course of a 17 month-long investigation. [The] report describes the obstruction and secrecy around the mpox proposal as a case study in how the institute "oversees and accounts for the monitoring of potentially dangerous gain-of-function research of concern." The revelations land amid global concerns about whether coronavirus gain-of-function research – research that might generate pathogens with increased pathogenicity or transmissibility – may have contributed to the worst pandemic in a century. The committee, in conjunction with the House Committee on Oversight and Reform, is also investigating coronavirus gain-of-function research underwritten by NIAID at the Wuhan Institute of Virology, and faces similar stonewalling in that investigation.

Note: Watch our 15-min Mindful News Brief video on the strong evidence that bioweapons research created COVID-19. For more along these lines, see concise summaries of deeply revealing news articles on COVID and government corruption from reliable major media sources.

Important Note: Explore our full index to revealing excerpts of key major media news stories on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.