Following FDA warning, Jubilant resolves quality issues
01 March 2014 | News | By BioSpectrum Bureau
Following FDA warning, Jubilant resolves quality issues
Jubilant Life Sciences has received a communication from the U.S. Food and Drug Administration (FDA), classifying its pharmaceutical manufacturing facility at Montreal, Canada as 'Acceptable'. The company announced the same on February 28, 2014.
"This resolves all issues raised by the FDA on the facility in February 2013 and subsequent communications. The development follows completionof FDA's review of the Company's responses post the February letter and the subsequent re-inspection conducted at Jubilant's Montreal facility in September, 2013. This development successfully resolves the FDA issues at our Montreal facility,"mentioned the statement from the Jubilant.
