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BioWorld - Thursday, April 30, 2026
Home » Topics » Regulatory » EMA

EMA
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Theratechnologies gives update on tesamorelin regulatory progress

June 25, 2012

European CHMP adopts opinion on teduglutide

June 25, 2012

Alexza provides update on Adasuve submissions

June 25, 2012

EMA validates MAAs for fixed-dose combination diabetes therapies

June 20, 2012

Investigational gene therapy gets orphan drug status for adrenoleukodystrophy

June 20, 2012

EMA to conduct centralized review of elvitegravir MAA

June 19, 2012

Genta reaches agreement on phase III tesetaxel trial

June 19, 2012

EMA's COMP issues opinion on Enhoxy

June 14, 2012

AR-42 gets E.U. orphan drug status for two additional indications

June 8, 2012

CHMP schedules hearing for Vivus' Qnexa MAA

June 6, 2012
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