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European Medicine Agency accepts Intas' Marketing Authorization Applicatio
Updated : 2 years, 8 months ago IST
Ahmedabad (Gujarat) [India], July 14: Intas Pharmaceuticals Ltd. announced that the European Medicine Agency (EMA) confirms acceptance of the Marketing Authorization Application (MAA) for DMB-3115, a biosimilar of Stelara® (Ustekinumab). The MAA has been submitted by Accord Healthcare,
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EMA safety committee probing cases of new side effect from AstraZeneca vac
Updated : 4 years, 10 months ago IST
Washington [US], May 7 (ANI/Sputnik): The European Medicine Agency (EMA) said on Friday that its committee on vaccine safety asked AstraZeneca to provide additional trial data on its COVID-19 drug for an inquiry into cases of a rare autoimmune disorder following vaccination.
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