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Elon Musk-owned Neuralink gets FDA approval for study of brain implants in humans | Oneindia News

Video Credit: Oneindia - Duration: 02:03s - Published
Elon Musk-owned Neuralink gets FDA approval for study of brain implants in humans | Oneindia News

Elon Musk-owned Neuralink gets FDA approval for study of brain implants in humans | Oneindia News

Elon Musk's start-up Neuralink on Thursday said it has gotten approval from US regulators to test its brain implants in people.

Neuralink said that clearance from the US Food and Drug Administration (FDA) for its first-in-human clinical study is ‘an important first step’ for its technology, which is intended to let brains interface directly with computers.

#Neuralink #ElonMusk #FDA ~PR.151~HT.98~ED.155~


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Oneindia Indian online news portal

Rahul Gandhi meets Danish Ali| 'Mohabbat ki Dukaan' message on Bidhuri remark| Oneindia News [Video]

Rahul Gandhi meets Danish Ali| 'Mohabbat ki Dukaan' message on Bidhuri remark| Oneindia News

In a heartwarming display of solidarity, Congress leader Rahul Gandhi paid a visit to Lok Sabha MP Danish Ali in Delhi. This visit comes in the wake of a disturbing incident where BJP MP Ramesh Bidhuri directed offensive comments towards Danish Ali. Bidhuri made objectionable remarks against Danish Ali in the Lok Sabha during a discussion on the Chandrayaan-3 mission. His comments drew huge outrage, and they have been expunged. #DanishAli #RahulGandhi #BJP #Congress #Parliament #DerogatoryRemarks #LokSabha #BJPMP #Controversy #PoliticalNews #IndianPolitics #RameshBidhuri #DanishAli #Islamophobia #RameshBidhuri, #LokSabhaSlurs ~HT.178~ED.101~GR.124~PR.152~

Credit: Oneindia    Duration: 03:09Published
Hangzhou Asian Games: Anurag Thakur cancels trip after China bars 3 Indian athletes | Oneindia News [Video]

Hangzhou Asian Games: Anurag Thakur cancels trip after China bars 3 Indian athletes | Oneindia News

India has filed a formal protest against China, this time because of sportsmanship or the lack thereof. According to reports, India is protesting against China’s ‘deliberate and selective obstruction of sportspersons’ after Beijing denied visas and accreditation to athletes from Arunachal Pradesh. The government said that Union Minister Anurag Thakur has also cancelled his visit to China. Three women wushu fighters are barred from entering China. #HangzhouAsianGames #China #ArunachalPradesh #IndiaChina ~HT.99~PR.151~ED.194~

Credit: Oneindia    Duration: 04:59Published
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World Cup 2023: Lokesh Kumar, Swiggy delivery guy picked for Netherlands cricket team |Oneindia News

Lokesh Kumar, a 29-year-old Swiggy delivery guy, recently found himself in an astonishing turn of events that led him to become a vital support staff member for the Netherlands Cricket Team. Please watch the video to know the story. #LokeshKumar #SwiggyDeliveryBoy #NetBowler ~HT.99~ED.194~PR.154~

Credit: Oneindia    Duration: 05:07Published
BSP MP Danish Ali slams BJP MP Ramesh Bidhuri’s communal slur in Lok Sabha | Oneindia News [Video]

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Ramesh Bidhuri of the Bharatiya Janata Party stirred a major political row after he allegedly made objectionable remarks against Bahujan Samaj Party MP Danish Ali in the Lok Sabha during a discussion on the Chandrayaan-3 mission on Thursday. Defence Minister Rajnath Singh expressed regret in the Lok Sabha for the objectionable remarks. #DanishAli #RameshBidhuri #BJP #Muslim #BSP #RameshBidhuriRemarks ~HT.99~PR.151~ED.155~

Credit: Oneindia    Duration: 14:39Published
Ramesh Bidhuri calls BSP's Danish Ali terrorist; Om Birla warns BJP MP over remarks | Oneindia News [Video]

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Ramesh Bidhuri of the Bharatiya Janata Party stirred a major political row after he allegedly made objectionable remarks against Bahujan Samaj Party MP Danish Ali in the Lok Sabha during a discussion on the Chandrayaan-3 mission on Thursday. Defence Minister Rajnath Singh expressed regret in the Lok Sabha for the objectionable remarks. #RameshBidhuri #DanishAli #BJP #Muslim #BSP ~HT.178~PR.151~ED.155~

Credit: Oneindia    Duration: 06:31Published

Elon Musk Elon Musk Business magnate (born 1971)

In a factory outside Glasgow, Scotland's answer to Musk's SpaceX is taking shape

A Scottish company hoping to take on SpaceX is just months away from launching a rocket in the Shetland Islands.
Sky News

Donald Trump Jr.'s Twitter Account Hacked, Announces Death of Donald Trump

Donald Trump Jr. might wanna get Elon Musk on the horn -- cuz he just got his X (formerly Twitter) account hacked -- sending out tweets about Biden, North Korea..
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Elon Musk's Neuralink to start human trial, to test brain chip in paralysis patients | Oneindia News [Video]

Elon Musk's Neuralink to start human trial, to test brain chip in paralysis patients | Oneindia News

Billionaire entrepreneur Elon Musk's brain-chip startup Neuralink said on Tuesday it has received approval from an independent review board to begin recruitment for the first human trial of its brain implant for paralysis patients.Please watch the video to know the details. #ElonMusk #Neuralink #Science ~PR.154~ED.194~HT.96~GR.124~

Credit: Oneindia    Duration: 03:03Published

Elon Musk's brain chip firm given all-clear to recruit for human trials

A brain chip company owned by Elon Musk has said it has received permission to start recruiting for human trials.
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Elon Musk Suggests All X Users , Will Soon Have to Pay a Fee. On Sept. 18, Musk and Israeli Prime Minister Benjamin Netanyahu livestreamed their conversation about AI. On Sept. 18, Musk and Israeli Prime Minister Benjamin Netanyahu livestreamed their conversation about AI. Amid their time together, Musk said, "We’re moving to having a small monthly payment for use of the X system... it’s the only way I can think of to combat vast armies of bots," 'Variety' reports. . Musk didn't offer a timeframe or an amount of what standard users would be charged, other than saying, "a few dollars or something.". Platform-wide subscription fees would also help to ease the pain of losing 50% of ad sales since Musk acquired the company. We’re still negative cash flow, due to ~50% drop in advertising revenue plus heavy debt load, Elon Musk, via July 15 post on X. X's current subscription program, X Blue, costs $8 a month. The tier provides a verified check mark, increased posting and editing capabilities, fewer ads, better rankings and more. Musk appointed Linda Yaccarino as CEO earlier this year. Musk appointed Linda Yaccarino as CEO earlier this year. She has since hired new sales executives in an attempt to set X on a better path. While Musk was at the helm, he let go of about 80% of staff

Credit: Wibbitz Top Stories    Duration: 01:30Published

Neuralink Neuralink American brain-computer interface company


Food and Drug Administration Food and Drug Administration United States federal agency

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CDC and FDA Recommend , Updated COVID Boosters for , Everyone Over Six Months Old. 'The Independent' reports that updated COVID boosters from both Pfizer and Moderna are now available at pharmacies across the United States. The Centers for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA) both recommend one dose of an updated vaccine for everyone over six months old. Depending on their previous vaccination status, both agencies say some children may be eligible for up to three doses. . 'The Independent' reports that both hospitalizations and deaths have been on the rise in the U.S. for weeks. At the same time, health authorities around the world are monitoring the emergence of two new variants, BA.2.86, known as Pirola, and EG.5, known as Eris. According to data from the CDC, Eris is now responsible for almost 25% of U.S. COVID cases, after first being detected in February. Meanwhile, Pirola has triggered a surge in cases across a number of countries, including the U.S. . The CDC warns that unvaccinated individuals are more likely to get severely ill if they are infected with COVID. The National Institutes of Health (NIH) strongly recommend that pregnant women get the updated vaccine, citing a recent study. The small study cited by the NIH found “protective antibodies in nearly 75% of infants born to women who had been vaccinated during pregnancy.”

Credit: Wibbitz Top Stories    Duration: 01:31Published
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DeSantis, Florida Surgeon General , Contradict Federal COVID Booster Guidance. On Sept. 11, the FDA approved a new COVID booster for anyone 6 months of age and older. The CDC recommended the new shots on Sept. 12. The vaccine is said to target Omicron subvariants that are spreading throughout the U.S. But Florida Gov. Ron DeSantis and Surgeon General Joseph A. Ladapo are advising the state's residents to not get the booster shot if they're under age 65, 'The Washington Post' reports. . The two men first made the comments during a live event last week and reiterated their claims during an X livestream on Sept. 13. . I will not stand by and let the FDA and CDC use healthy Floridians as guinea pigs for new booster shots that have not been proven to be safe or effective. No way FDA, Gov. Ron DeSantis, via X livestream. In December, DeSantis said he was forming a panel to counter the CDC's health recommendations, implying that the public has been misled about vaccine efficacy, 'The Washington Post' reports. . In May, he barred vaccine passports and mask requirements in schools and businesses. Ladapo has long been skeptical about COVID vaccines as well. In the past, his warnings were met with a public letter written by the FDA and CDC, . In the past, his warnings were met with a public letter written by the FDA and CDC, . saying that his comments were "incorrect, misleading and could be harmful to the American public," 'The Washington Post' reports.

Credit: Wibbitz Top Stories    Duration: 01:30Published
FDA Warns Companies to Stop Selling Potentially Dangerous, Unapproved Eye Drops [Video]

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FDA Warns Companies to, Stop Selling Potentially Dangerous, , Unapproved Eye Drops. Gizmodo reports that the United States Food and Drug Administration (FDA) has warned several companies to stop selling unapproved eye drop products. On September 12, the FDA announced that it had issued warning letters to eight companies regarding the potentially dangerous products. The companies, including major retail chains CVS and Walgreens, have allegedly committed a number of violations by marketing or manufacturing these products. The companies, including major retail chains CVS and Walgreens, have allegedly committed a number of violations by marketing or manufacturing these products. The companies, including major retail chains CVS and Walgreens, have allegedly committed a number of violations by marketing or manufacturing these products. The FDA has also expressed concerns over silver compounds found in some of the products, which can turn people's skin or eyes blue with long-term use. According to the FDA, some of the eye drop products were allegedly manufactured at facilities that have failed to meet standard safety and quality guidelines. The FDA is particularly concerned that these illegally marketed, unapproved ophthalmic drug products pose a heightened risk of harm to users because drugs applied to the eyes bypass some of the body’s natural defenses, Food and Drug Administration, via statement. The FDA is particularly concerned that these illegally marketed, unapproved ophthalmic drug products pose a heightened risk of harm to users because drugs applied to the eyes bypass some of the body’s natural defenses, Food and Drug Administration, via statement. Gizmodo reports that the companies have 15 days to respond with their plans to correct the alleged violations. If the companies fail to respond, the FDA could take further action to either seize or stop the manufacturing of the products in question. When we identify illegally marketed, unapproved drugs and lapses in drug quality that pose potential risks, the FDA works to notify the companies involved of the violations, Jill Furman, Director of the Office of Compliance for the FDA’s Center for Drug Evaluation and Research, via Gizmodo. We will continue to investigate potentially harmful eye products and work to ensure violative products stay off store shelves so that consumers can continue taking the medicines they need without concern, Jill Furman, Director of the Office of Compliance for the FDA’s Center for Drug Evaluation and Research, via Gizmodo. We will continue to investigate potentially harmful eye products and work to ensure violative products stay off store shelves so that consumers can continue taking the medicines they need without concern, Jill Furman, Director of the Office of Compliance for the FDA’s Center for Drug Evaluation and Research, via Gizmodo

Credit: Wibbitz Top Stories    Duration: 01:30Published
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FDA Says Popular Nasal Decongestant Not Effective Treatment For Congestion

FDA Says Popular , Nasal Decongestant , Not Effective Treatment For Congestion. Associated Press reports that government experts found that the number one decongestant in the United States does not alleviate a stuffy nose. . Associated Press reports that government experts found that the number one decongestant in the United States does not alleviate a stuffy nose. . On September 12, advisers for the Food and Drug Administration voted unanimously against the effectiveness of phenylephrine. Phenylephrine is found in a number of popular over-the-counter products, including Sudafed, Allegra and Dayquil. Modern studies, when well conducted, are not showing any improvement in congestion with phenylephrine, Dr. Mark Dykewicz, Allergy specialist at the Saint Louis University School of Medicine, via Associated Press. AP reports that a team of outside advisers were assembled by the FDA to take a closer look at the effectiveness of phenylephrine. Phenylephrine became the key ingredient in decongestants in 2006, when pseudoephedrine was ordered to be moved behind pharmacy counters. Phenylephrine became the key ingredient in decongestants in 2006, when pseudoephedrine was ordered to be moved behind pharmacy counters. The change came after a 2006 law called for the change, as pseudoephedrine can be used to produce methamphetamine. . The change came after a 2006 law called for the change, as pseudoephedrine can be used to produce methamphetamine. . AP reports that pending the FDA's decision, drugmakers like Johnson & Johnson and Bayer could be ordered to pull oral medications with phenylephrine. . AP reports that pending the FDA's decision, drugmakers like Johnson & Johnson and Bayer could be ordered to pull oral medications with phenylephrine. . According to the FDA's panel of experts, consumers would need to be educated on remaining options for treating congestion. Patients require and deserve medications that treat their symptoms safely and effectively and I don’t believe that this medication does that, Jennifer Schwartzott, the patient representative on the FDA panel, via Associated Press

Credit: Wibbitz Top Stories    Duration: 01:31Published
FDA Approves New COVID Boosters Ahead of Expected Winter Surge in Cases [Video]

FDA Approves New COVID Boosters Ahead of Expected Winter Surge in Cases

FDA Approves New COVID Boosters , Ahead of Expected Winter Surge in Cases. On September 11, the United States Food and Drug Administration approved updated COVID boosters from both Pfizer and Moderna. NBC reports that the new boosters are specifically formulated to target the XBB.1.5 subvariant. . The updated shots are expected to be available later this week, pending the approval of the Centers for Disease Control and Prevention. According to the FDA, anyone over the age of five is eligible to receive either company's booster shot, regardless of if they were previously vaccinated. The FDA also advised that vaccinated individuals should wait at least two months before receiving the updated booster. . NBC reports that the news comes as the U.S. faces a rising number of cases, as a result of a number of new subvariants. Officials have expressed hope that the new boosters could potentially stave off a spike in winter infections. . On September 12, a CDC advisory committee is scheduled to convene for a vote on recommendations for who should receive the booster. . On September 12, a CDC advisory committee is scheduled to convene for a vote on recommendations for who should receive the booster. . NBC reports that CDC Director Dr. Mandy Cohen is expected to approve those recommendations, opening the door for vaccinations to begin. NBC reports that CDC Director Dr. Mandy Cohen is expected to approve those recommendations, opening the door for vaccinations to begin. According to experts, those who haven't had a booster since last fall, as well as those who haven't had a recent case of COVID, should get the booster as soon as possible.

Credit: Wibbitz Top Stories    Duration: 01:31Published

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