Mumbai (Maharashtra) [India], Jun 1 (ANI): After a video, of a street food vendor using tap water from a railway station toilet here to prepare food, was widely shared on social media, the Food and Drug Administration (FDA) has initiated an inquiry. It has also issued a public warning agains
Noida (Uttar Pradesh) [India], Mar 8 (ANI): Jubilant Life Sciences said on Friday that the US Food and Drug Administration (USFDA) has issued a warning letter after conducting an inspection at its manufacturing facility in Roorkee, Uttarakhand.
New Delhi [India], Feb 26 (ANI): Aavis Pharmaceuticals, part of Espee Group, located in Hoschton, GA, completed an inspection by the US Food and Drug Administration at the company’s primary manufacturing facility with Zero 483 observations. With successful inspection of its formulat
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
Chandigarh [India], Dec 24 (ANI): India is fast emerging as an inventors' hub for patents for an assortment of drugs worldwide. Around 15 per cent of the total 1.3 lakh patents filed in India from 2013 to 2015 have been contributed by the indigenous pharmaceutical industry. India is ranked
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)
New Delhi [India], May 8 (ANI-NewsVoir): Parry Nutraceuticals (a division of EID Parry and part of the Murugappa Group) has received the U.S. Food and Drug Administration (US-FDA) approval for its India facility for organic microalgae cultivation and processing.