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Home Articles FDA
‘Operation Fly Formula’: Biden invokes wartime act to address infant formula shortage \
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‘Operation Fly Formula’: Biden invokes wartime act to address infant formula shortage

 19-May-2022
Washington [US], May 19 (ANI): US President Joe Biden on Wednesday (local time) invoked the Defense Production Act to ramp up the production of infant formula in the wake of growing safety concerns over quality of infant foods following death of two babies and subsequent shortage caused by supply chain bottlenecks.
19-May-2022 World
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NeoImmuneTech obtains approval for phase 2 trial of brain tumor treatment from US FDA \
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NeoImmuneTech obtains approval for phase 2 trial of brain tumor treatment from US FDA

 12-May-2022
Seoul [South Korea], May 12 (ANI/Global Economic): NeoImmuneTech said on the 11th that it has obtained the approval for a phase 2 clinical trial plan that concomitant administration of US Merck's immune checkpoint inhibitor Keytruda and its T-cell amplifier NT-I7 to patients with glioblastoma from the United States Food & Drug Administration (US FDA).
12-May-2022 World
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FDA restricts J&J COVID-19 vaccine due to blood clot risk \
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FDA restricts J&J COVID-19 vaccine due to blood clot risk

 06-May-2022
U.S. regulators on Thursday strictly limited who can receive Johnson & Johnson’s COVID-19 vaccine The restriction was due to a rare but dangerous risk of blood clots. The vaccination should only be administered to people who are unable to obtain another vaccine or who specifically prefer J&J’s vaccine, according to the FDA. For months, US […]
06-May-2022 World
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Radiofrequency spinal cord stimulation shows improved longer-lasting pain relief: Study \
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Radiofrequency spinal cord stimulation shows improved longer-lasting pain relief: Study

 29-Apr-2022
San Diego (California) [US], April 29 (ANI): According to a new study, chronic pain spinal cord stimulation (SCS) uses an implanted device to supply a small amount of electricity directly to the spinal cord, altering or blocking nerve activity and minimizing the sensation of pain reaching the brain.
29-Apr-2022 Health
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China’s President Xi Jinping is in a Bind over Who’s to Blame for Shanghai’s Virus … – Latest Tweet by Bloomberg \
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China’s President Xi Jinping is in a Bind over Who’s to Blame for Shanghai’s Virus … – Latest Tweet by Bloomberg

 29-Apr-2022
China's President Xi Jinping is in a bind over who's to blame for Shanghai's virus outbreak. An obvious scapegoat is one of his close allies. https://t.co/WRsnDKnKSy China’s President Xi Jinping is in a Bind over Who’s to Blame for Shanghai’s Virus … – Latest Tweet by Bloomberg — Bloomberg (@business) April 29, 2022 Eli Lilly […]
29-Apr-2022 Business
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Eli Lilly Will Ask the FDA for Accelerated Approval of Its Experimental Alzheimer’s … – Latest Tweet by Bloomberg \
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Eli Lilly Will Ask the FDA for Accelerated Approval of Its Experimental Alzheimer’s … – Latest Tweet by Bloomberg

 28-Apr-2022
Eli Lilly will ask the FDA for accelerated approval of its experimental Alzheimer’s treatment before July https://t.co/XKL1y7oO8n Eli Lilly Will Ask the FDA for Accelerated Approval of Its Experimental Alzheimer’s … – Latest Tweet by Bloomberg — Bloomberg (@business) April 28, 2022 Gujarat Shocker: Class 9 Student of Kendriya Vidyalaya Forced To Drink Urine by […]
28-Apr-2022 Business
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FDA authorizes first-ever breathing test for detecting COVID-19 infection \
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FDA authorizes first-ever breathing test for detecting COVID-19 infection

 16-Apr-2022
Washington [US], April 16 (ANI): The Food and Drug Administration (FDA) authorized the first test, InspectIR COVID-19 Breathalyzer, to detect COVID-19 through the breath for emergency use.
16-Apr-2022 World
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US FDA approves emergency use of first COVID-19 test that uses breath samples \
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US FDA approves emergency use of first COVID-19 test that uses breath samples

 15-Apr-2022
A COVID-19 diagnostic test has come to light that uses breath samples to generate a positive or negative result. It has received emergency use authorization from the US Food and Drug Administration (FDA). Dubbed ‘InspectIR’, this breath analyzer COVID-19 test detects chemical components linked to coronavirus in breath samples. “Today’s authorization is yet another example […]
15-Apr-2022 World
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FDA grants Direct Biologics regenerative Medicine Advanced Therapy (RMAT) Designation for the use of ExoFlo in COVID-19 Related ARDS \
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FDA grants Direct Biologics regenerative Medicine Advanced Therapy (RMAT) Designation for the use of ExoFlo in COVID-19 Related ARDS

 13-Apr-2022
Austin (Texas) [US], April 13 (ANI/PRNewswire): Direct Biologics, an innovative biotechnology company with a groundbreaking extracellular vesicle (EV) platform drug technology, announced that the U.S. Food and Drug Administration (FDA) has awarded their EV drug product ExoFlo with a Regenerative Medicine Advanced Therapy (RMAT) designation for the treatment of Acute Respiratory Distress Syndrome (ARDS) associated with COVID-19.
13-Apr-2022 Business
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This World Health Day, let walnuts help you in making everyday healthy \
6 min read
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This World Health Day, let walnuts help you in making everyday healthy

 07-Apr-2022
New Delhi [India], April 7 (ANI/NewsVoir): The shift in purchasing power and technology may have made our lives easier and faster - but has it made our lives better? Well, not 100 per cent, if you ask me. In fact, we are left with over-exploited resources, tighter schedules, and little to no physical activity. A result of which is a variety of lifestyle diseases.
07-Apr-2022 Business
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