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BioWorld - Tuesday, July 21, 2026
Home » Topics » Regulatory » EMA

EMA
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EMEA withdraws marketing authorization for Protopy in the European Union

Oct. 9, 2008

CHMP recommends variations to marketing authorization of Cancidas

Sep. 30, 2008

CHMP recommends marketing authorization for Azarga in open-angle glaucoma

Sep. 30, 2008

GSK withdraws European MAA for Quintanrix vaccine

Sep. 3, 2008

EMEA presents an update on reports of PML in MS patients treated with Tysabri

Aug. 14, 2008

CHMP recommends marketing authorization for GSK's prepandemic influenza vaccine

July 30, 2008

Anticoagulant Xarelto recommended for approval in E.U.; NDA submitted in U.S.

July 30, 2008

CHMP recommends refusal of Santhera's MAA for Sovrima in Friedreich's ataxia

July 30, 2008

CHMP adopts negative opinion for Howmedica's Opgenra

July 4, 2008

EMEA recommends that product information for Pfizer's Exubera include data on lung cancer

June 19, 2008
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