Food and Drug Administration
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FDA Proposes Annual COVID Vaccination Plan
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Elon Musk's Neuralink Seeks Approval to Begin Human Trials
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HC quashes J&J baby powder manufacture ban over FDA test delay
Zydus’ US arm gets final nod from USFDA for anti-seizure drug
FDA Warns TikTokers to Stop Cooking NyQuil-Marinated ChickenThe FDA is warning TikTokers who are jumping on the latest craze to beware ... because NyQuil-marinated chicken is a dangerous thing. It sounds as disgusting as it is dangerous ... "sleepy chicken" is..
Juul E-Cigarettes To Be Banned In the U.S., WSJ ReportJuul e-cigarettes will soon be off the shelves, at least according to a report, that states the FDA is planning to ban the product from being sold in the U.S. The Wall Street Journal reports the Food..
FDA lifts hold on Covaxin's clinical trials in USThe US Food and Drug Administration which has put on hold the phase 2/ 3 clinical trials of Bharat Biotech's Covid-19 vaccine Covaxin, in USA, has lifted the pause, according to a statement issued by..
Covaxin Phase 2&3 trials to resume in US after USFDA lifts clinical holdThe US Food and Drug Administration (USFDA) has lifted the clinical hold on the Phase 2 and 3 immuno-bridging clinical trials of Bharat Biotech’s Covid-19 vaccine Covaxin that were being conducted in..
FDA Investigating Lucky Charms, People Think Cereal Made Them SickScores of people say they've fallen ill after eating a bowl of Lucky Charms ... and now the feds are investigating the popular cereal. The U.S. Food and Drug Administration announced Monday the agency..
Fallout of WHO observations: Covaxin's Phase 2/3 trials in US put on holdThe US Food and Drug Administration has put on hold the phase 2/3 clinical trials of Bharat Biotech's Covid-19 vaccine Covaxin, in USA. Bharat Biotech's partner for US and Canada for Covaxin, the FDA's..
USFDA paves way for Covaxin trials in US
USFDA lifts clinical hold on Ocugen's IND application for Covaxin paving way for its evaluation for US market
USFDA nod to clear way for Molnupiravir use in India
Zydus Cadila gets USFDA nod to market generic cancer drug in US
Biden picks former FDA chief Califf to again lead agency
Bharat Biotech partner Ocugen seeks USFDA nod for Covaxin EUA for kids
Bharat Biotech's US partner Ocugen files EUA request with FDA for paediatric use of Covaxin
Covid-19: Travellers vaccinated with Covaxin can enter USCDC press officer, Scott Pauley said, "CDC's travel guidance applies to FDA approved or authorized and WHO Emergency Use Listing vaccines and encompasses any new vaccines that may be added to either of..
Ocugen files Covaxin IND application with USFDA, seeks nod for Phase-3 trial in US
Joe Rogan Has COVID, Cancels Show & Admits He's on IvermectinJoe says he's taking ivermectin -- the livestock de-wormer drug that the CDC and the FDA have specifically come out and warned against as a remedy to battle COVID. 🤷🏽♂️ Joe Rogan's..
'You are not a horse or a cow': Health officials warn against using livestock de-worming drug to treat COVID-19The US Food and Drug Agency (FDA) has issued a warning to people not to take an anti-parasitic drug designed for livestock to treat or prevent COVID-19 following multiple reports of poisonings.
Ocugen to take BLA route for Covaxin in US based on FDA recommendation; seek emergency use nod for CanadaBharat Biotech’s US partner Ocugen has dropped its plans of applying for an emergency use authorisation (EUA) for indigenously developed Covaxin and will be pursuing the biologics license application..
Covaxin's US approval delayed as FDA asks for more dataOcugen Inc said on Thursday it would no longer pursue an emergency use authorization for its Covid-19 vaccine candidate, Covaxin, and would instead aim to file for a full US approval of the shot...
DCGI waiver likely to bring foreign vaccines like Pfizer, Moderna a step closerIn a letter, DCGI Chief VG Somani letter said that this will be applicable for vaccines that have already been approved for restricted use by the US FDA, EMA, UK MHRA, PMDA Japan or listed for..
Uddhav Thackeray shunts FDA chief over Covid drug row
What is Remdesivir and is the drug really useful in treating COVID-19? All you need to knowRemdesivir was approved as the first drug to treat the virus by the US Food and Drug Administration in 2020.
Govt fast-tracks nod for Covid vaccination cleared in other countriesWith surging Covid-19 cases fuelling calls for faster vaccination, the Centre on Tuesday enabled faster access to foreign-made vaccines by doing away with bridging trial studies prior to grant of..
US recommends 'pause' to Johnson & Johnson jab rollout over blood clot fearsThe US Food and Drug Administration has recommended a "pause" to the rollout of the Johnson & Johnson COVID vaccine so it can investigate reports of blood clots.
Karnataka: KPSC FDA exam postponed after question paper leak, six heldThe dates for the test would be rescheduled and announced in due course, a press release said.
Johns Hopkins Professor Says U.S. COVID Response is Like 'Operation Turtle Speed'Operation Warp Speed is a misnomer, according to a Johns Hopkins doctor ... the frustrated doc says it's more like Operation Turtle Speed. Professor Marty Makary is angry the FDA hasn't gone the route..
USFDA may give impetus to plasma therapy in India, experts question efficacy
Zydus Cadila gets USFDA nod for drug trials to treat chemotherapy-induced anemiaIn a regulatory filing, Zydus Cadila said it has received approval from the US Food and Drug Administration (USFDA) to initiate clinical trials of Desidustat in CIA. Zydus Cadila Chairman Pankaj R..
FDA warns against combination of malaria drug and Gilead's remdesivirThe U.S. Food and Drug Administration on Monday issued a warning to healthcare providers against administering malaria drug hydroxychloroquine or chloroquine in combination with Gilead Sciences'..
India approves emergency use of remdesivir to treat Covid-19 patientsRemdesivir is the first drug to show improvement in Covid-19 patients in formal clinical trials. It was granted emergency use authorization by the US Food and Drug Administration last month and has..
NRI’s disinfectant tech gets US-FDA nod for medical useThe device — Molekule Air Pro RX — built by US firm Molekule based on technology developed by Yogi Goswami, has now been approved by the US Food and Drugs Administration (US-FDA) for medical use..
Roche wins U.S. nod for COVID-19 antibody test, aims to boost outputRoche has won emergency approval from the U.S. Food and Drug Administration (FDA) for an antibody test to determine whether people have ever been infected with the coronavirus, the Swiss drugmaker on..
US OKs remdesivir; India plans trialsThe US Food and Drug Administration has allowed emergency use of the experimental anti-viral drug remdesivir, previously used for Ebola, to treat Covid-19 patients even as India is looking to import..
'UN chief Guterres salutes countries like India for helping others in fight against Covid-19'UN Secretary-General Antonio Guterres salutes countries helping others in the global fight against the COVID-19 pandemic, his spokesman has said, days after India sent supplies of the anti-malarial..
Indian test kits may be non-starterNIV Validating Them But Govt Insists On USFDA Or EU Nod
Pvt labs with USFDA-approved kits can start testing for Covid-19The government has decided that private laboratories with Covid-19 testing kits approved by the US Food and Drug Administration (US FDA) can start testing suspected cases, significantly adding to the..
Make-in-India: Indo-US firm gets nod to test Covid-19 KitAn Indo-US firm — CoSara Diagnostics — based out of Baroda and supported by Bengaluru-based Centre for Cellular And Molecular Platforms (CCAMP) has developed a diagnostic kit for Covid-19, which..
FDA works to speed coronavirus tests with Roche, New York approvalsThe U.S. Food and Drug Administration (FDA) issued emergency authorization for a faster coronavirus test made by Swiss diagnostics maker Roche and allowed New York state to authorize certain labs to..
New Roche coronavirus test wins emergency U.S. approvalThe U.S. Food and Drug Administration (FDA) issued emergency authorization for a faster coronavirus test made by Swiss diagnostics maker Roche , a move aimed at boosting screening capacity to help..
United States approves coronavirus test in race to boost screening capacityThe U.S. Food and Drug Administration issued emergency authorization for a coronavirus test made by Swiss diagnostics maker Roche , a move aimed at boosting screening capacity to help contain the..
U.S. FDA official warns of possibility of coronavirus pandemicA U.S. Food and Drug Administration official on Wednesday pointed to the spread of the new coronavirus to six of the world's seven continents as he warned of the potential for a global pandemic.
U.S. expands use of coronavirus diagnostic testThe U.S. Food and Drug Administration on Tuesday granted emergency use approval for state public health laboratories to start testing for the new flu-like coronavirus from China using kits developed by..