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BioWorld - Monday, February 2, 2026
Home » Topics » Regulatory » EMA

EMA
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Alexza provides regulatory update for Staccato Loxapine

Dec. 10, 2010

European approval of Brilique for prevention of atherothrombotic events

Dec. 10, 2010

UCB updates progress from third quarter of 2010

Dec. 1, 2010

FDA clears design of phase III oritavancin trials SOLO-1 and -2

Dec. 1, 2010

New Juvista formulation for children significantly improves scar appearance

Nov. 23, 2010

CIS Bio withdraws E.U. marketing authorization for NeoSpect

Nov. 23, 2010

EMA's COMP recommends orphan status for paquinimod in systemic sclerosis

Nov. 18, 2010

EMA accepts Pixuvri MAA for non-Hodgkin's lymphoma for review

Nov. 18, 2010

Roche reports on third quarter of 2010

Nov. 18, 2010

EMA approves Cell Therapeutics' pediatric investigation plan for Pixuvri

Nov. 17, 2010
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