Trump claim tylenol sutism risk

Speaking from the Oval Office, Trump stated that the US Food and Drug Administration (FDA) would soon notify...

Zumutor Biologics Inc announces FDA clearance of IND application

Boston [US]/Bangalore (Karnataka) [India], August 11: Zumutor Biologics Inc "Zumutor", a Boston based...

US FDA Grants Breakthrough Designation for Blood Test

Mumbai (Maharashtra) [India], January 3 (ANI/PRNewswire): Datar Cancer Genetics announced today that the US Food and...

Magnum receives USFDA 510k clearance for its surgical masks

New Delhi [India], August 26 (ANI/SRV): Magnum, one of the largest mask manufacturers from Mumbai, which has been in...

FDA denies authorization to market JUUL e-cigarettes

Maryland [US], June 24 (ANI): Citing safety concerns, the US Food and Drug Administration (FDA) issued marketing...

US approves Covid-19 vaccines for youngest children

Washington [US], June 17 (ANI): The US Food and Drug Administration (FDA) authorized emergency use of the Moderna...

FDA removes clinical hold on phase 2,3 clinical trial for COVAXIN

Malvern (Pennsylvania) [US], May 23 (ANI): Biotechnology company Ocugen on Monday announced that the US Food and...

US FDA limits use of Johnson & Johnson COVID-19 vaccine

Washington [US], May 6 (ANI): The US Food and Drug Administration (FDA) on Thursday said that the Johnson &...

COVID-19: FDA gives clearance to Covaxin for clinical trials...

New Delhi [India], March 7 (ANI): Bharat Biotech's COVID-19 vaccine Covaxin has been given clearance for clinical...

US FDA grants the coveted Breakthrough Designation for...

Mumbai (Maharashtra) [India], February 15 (ANI/PR Newswire): Datar Cancer Genetics today announced that the US Food...

US grants emergency use authorization for Merck's COVID-19 pill

Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Thursday said that it has granted...

US FDA authorizes Pfizer's COVID antiviral pill for people aged 12

.Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Wednesday (local time) authorized...