Mumbai (Maharashtra) [India], Feb 2 (ANI): Rais Shaikh, a corporator from Mumbai, who represents the Samajwadi Party, wrote a letter on Saturday to the city's Municipal Commissioner Ajoy Mehta and the Food and Drugs Administration (FDA) stating that a signboard should be placed at restaurant
California [United States], January 19 (ANI): After Apple, Google's parent company Alphabet is working its way towards bringing health at the center of its products. Now, the company's health division Verily has reportedly received FDA 510(k) clearance for its Study smartwatch for an on-dema
New Delhi [India], Oct 31 (ANI-BusinessWireIndia): Gupta Oxygen Pvt. Ltd., a pioneer in industrial, medical and refrigeration gases today announced the launch of the first ever FDA approved canned Oxygen, MyOxy exclusively for the India market.
Gujarat [India], Oct 11 (ANI-BusinessWireIndia): Concept Medical Inc. has approached the FDA for an Investigational Device Exemption (IDE) for their Sirolimus-Coated Balloon (DCB).
Massachusetts [United States], September 14 (ANI): If you are still skeptical about owning a smartwatch, it may just be the time to do so. According to the latest estimates by market researcher IDC, smartwatches are set to dominate nearly half of the entire wearables market by 2022.
Washington DC, [USA] Sep 01 (ANI): The US Food and Drug Administration, on Thursday, issued a safety alert warning the consumers against eating food prepared with liquid nitrogen.
Washington DC, [USA] July 31 (ANI): The US Food and Drug Administration (FDA) has warned against the use of devices that promise 'vaginal rejuvenation', stating that it can cause serious effects.
New Delhi [India], July 30 (NewsVoir): Morepen Laboratories Ltd. has received US FDA (United States Food and Drug Administration) approvals for both its bulk drugs manufacturing facilities situated in Himachal Pradesh.
Washington D.C. [USA], May 31 (ANI): United States President Donald Trump on Wednesday signed a major drug bill called "Right to Try" for terminally ill patients, allowing them to go for experimental medical treatments, which is not yet approved by the US Food and Drug Administration (FDA
Bengaluru (Karnataka) [India], Feb 28 (Businesswire India): Giving a fillip to the Government's 'Make in India' initiative, Axiostat has become the first Indian wound care product to receive 510(K) FDA clearance in the US for its pioneering haemostatic dressing.
Ahmedabad (Gujarat) [India], Jan 4 (ANI-NewsVoir): A milestone for the history of interventional cardiology field in India has been achieved by world renowned Interventional Cardiologist Dr. Tejas Patel, Chairman and Chief Interventional Cardiologist at Apex Heart Institute, Ahmedabad. He an
New Delhi [India], Dec 20 (ANI-NewsVoir): The United States Food and Drug Administration (USFDA) has cleared Montelukast Sodium, a bulk drug / API manufactured by Morepen Laboratories Ltd., for sale in the US market. This gives Morepen an entry into the Rs. 2000 crore (Approx. $ 300 million)