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BioWorld - Saturday, June 13, 2026
Home » Topics » Regulatory » EMA

EMA
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EMA recommends approval of Sanofi Pasteur pediatric vaccine

Feb. 27, 2013

EMA confirms decision on VIVUS' MAA for obesity treatment

Feb. 25, 2013

EMA grants orphan designation to BHR Pharma's investigational agent for traumatic brain injury

Feb. 14, 2013

Prolor Biotech's hGH-CTP receives orphan drug designation in Europe

Feb. 14, 2013

Pediatric indication of Ixiaro approved in Europe

Feb. 12, 2013

EMA committee begins safety review of Diane-35 and generics

Feb. 11, 2013

EMA grants accelerated assessment to trametinib application

Feb. 8, 2013

EMA approves label extension for Abilify

Feb. 6, 2013

French ANSM to suspend marketing of Diane-35 and generics for acne

Jan. 31, 2013

Prosensa's Duchenne muscular dystrophy products achieve orphan drug status

Jan. 30, 2013
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