New Delhi [India], July 26: In a major stride towards improving women's healthcare, Nesa Medtech, a prominent startup in women’s health, has announced that its groundbreaking Fibroid Mapping Reviewer Application (FMRA) has received 510(k) clearance from the U.S. Food and Drug Administration
Bengaluru (Karnataka) [India], July 24: Nesa Medtech (Nesa), a private medical device company addressing clinical unmet needs for patients with symptomatic uterine fibroids, announced today that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the company's F
Conducted in June 2023, Operation Broader Sword stopped more than 500 shipments of illicit, and potentially dangerous, unapproved prescription drugs, combination medical devices, and synthetic drug precursors from reaching American consumers, the US Embassy in India said in a press release.
In a tweet, Neuralink expressed its excitement, "We are excited to share that we have received the FDA's approval to launch our first-in-human clinical study! This is the result of incredible work by the Neuralink team in close collaboration with the FDA and represents an important first
"Food And Drug Administration (FDA) of Punjab doubt that someone has duplicated the product (cough syrup) sent to Cambodia and then sold it in the Marshall Islands and Micronesia to defame the Government of India," said Sudhir Pathak, MD of the firm based in Dera Bassi, Punjab .
San Diego (California) [US], April 19 (ANI/PRNewswire): Ajinomoto Bio-Pharma Services ("Aji Bio-Pharma"), a leading provider of biopharmaceutical contract development and manufacturing services, is pleased to announce that the United States Food and Drug Administration (FDA) has approved the
Soon after an appeals court judgement that limited an earlier ruling that would have revoked the abortion pill's clearance for use, the US Department of Justice (DOJ) will move the Supreme Court to stop limits on the sale of mifepristone, Al Jazeera reported.
Azithromycin is prescribed to treat certain bacterial infections such as bronchitis, pneumonia, sexually transmitted diseases (STD), and infections of the ears, lungs, sinuses, skin, throat, and reproductive organs.
The deal for NJOY, one of the few e-cigarette makers whose products have clearance from federal regulators, includes an additional USD 500 million if the Food and Drug Administration authorises additional NJOY products.
Maharashtra's Food and Drug Administration on Friday said it issued show cause notices to 17 companies manufacturing cough expectorants, instructed four companies to stop their production and terminated licences of six companies.
After the US regulator Food and Drug Administration warned consumers "not to purchase or use EzriCare Artificial Tears due to potential contamination", the Central Drugs Standard Control Organization (CDSCO) under the Union Health ministry and the Tamil Nadu State Drug Controller have ini