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BioWorld - Friday, April 24, 2026
Home » Topics » Regulatory » EMA

EMA
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GSK withdraws indication extension application for Tyverb

Feb. 17, 2012

CPP-115 receives European orphan drug status

Feb. 14, 2012

Alexza Pharmaceuticals receives first feedback on Adasuve MAA

Feb. 14, 2012

Navidea Biopharmaceuticals receives CHMP advice on Lymphoseek MAA

Feb. 2, 2012

Indication for Gadovist 1.0 is expanded

Jan. 30, 2012

Novartis reflects on accomplishments of 2011

Jan. 30, 2012

CHMP issues opinion on Remicade for ulcerative colitis in children

Jan. 26, 2012

CHMP recommends updating Glivec label in Europe

Jan. 24, 2012

EMA recommends marketing suspension for meprobamate-containing medicines

Jan. 23, 2012

EMA reviews Gilenya following reports of heart problems in patients

Jan. 23, 2012
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