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BioWorld - Thursday, June 18, 2026
Home » Topics » Regulatory » EMA

EMA
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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

MultiStem receives orphan drug designation in Europe

Dec. 18, 2013

EMA accepts Fibrocaps MAA for review

Nov. 29, 2013

EMA grants accelerated assessment to faldaprevir

Nov. 27, 2013

Celgene receives positive CHMP opinion for Abraxane in combination with gemcitabine

Nov. 26, 2013
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