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BioWorld - Thursday, May 7, 2026
Home » Topics » Regulatory » EMA

EMA
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EMA committee recommends suspending use of Protelos/Osseor

Jan. 15, 2014

EMA accepts Biovest's MAA for BiovaxID

Jan. 14, 2014

Fenfluramine obtains orphan drug designation in the U.S. and E.U. for Dravet syndrome

Jan. 10, 2014

EMA grants accelerated review to Bristol-Myers' MAA for daclatasvir in chronic HCV

Jan. 10, 2014

Cytovir ADV ready to receive orphan drug designation in Europe

Jan. 8, 2014

CHMP gives positive opinion on subcutaneous tocilizumab

Dec. 27, 2013

EMA accepts tolvaptan MAA for ADPKD

Dec. 27, 2013

EMA accepts dalbavancin MAA for review

Dec. 24, 2013

EMA accepts filing of MAA for cangrelor

Dec. 24, 2013

Cometriq receives positive CHMP opinion for thyroid carcinoma

Dec. 23, 2013
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