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Archive:
European Medicines Agency
Showing 231 to 240 of 575 entries
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Title
2012-03-16
Press Release: European Medicines Agency confirms positive benefit-risk balance of Protelos/Osseor but recommends new contraindications and revised warnings
Author (Corporate):
European Medicines Agency
Series Details:
Press Release
EMA/CHMP/185175/2012 (16.3.12)
Published:
16/03/2012 (Last update: 16/03/2012)
2012-03-05
Press Release: European Medicines Agency publishes updated set of mandatory Article 57(2) requirements for marketing authorisation holders
Author (Corporate):
European Medicines Agency
Series Details:
Press Release
EMA/139333/2012 (5.3.12)
Published:
05/03/2012 (Last update: 05/03/2012)
2012-03-01
European Medicines Agency publishes list of human medicines under evaluation
Author (Corporate):
European Medicines Agency
Series Details:
News
1.3.12
Published:
01/03/2012 (Last update: 01/03/2012)
2012-02-29
European Medicines Agency launches call for expression of interest from healthcare professional organisations
Author (Corporate):
European Medicines Agency
Series Details:
News
29.2.12
Published:
29/02/2012 (Last update: 29/02/2012)
2012-02-22
European Medicines Agency releases good pharmacovigilance practice modules for public consultation
Author (Corporate):
European Medicines Agency
Series Details:
News
22.2.12
Published:
22/02/2012 (Last update: 22/02/2012)
2012-02-17
Press Release: European Medicines Agency recommends new contraindications and warnings for aliskiren-containing medicines
Author (Corporate):
European Medicines Agency
Series Details:
Press Release
EMA/CHMP/112042/2012 (17.2.12)
Published:
17/02/2012 (Last update: 17/02/2012)
2012-02-17
Press Release: European Medicines Agency recommends lifting suspension of aprotinin
Author (Corporate):
European Medicines Agency
Series Details:
Press Release
EMA/CHMP/119704/2012 (17.2.12)
Published:
17/02/2012 (Last update: 17/02/2012)
2012-02-17
Press Release: European Medicines Agency recommends new anti-malaria treatment for use outside the European Union
Author (Corporate):
European Medicines Agency
Series Details:
Press Release
EMA/CHMP/114875/2012 (17.2.12)
Published:
17/02/2012 (Last update: 17/02/2012)
2012-02-17
Press Release: European Medicines Agency concludes review of dose recommendations for anti-tuberculosis medicines used in children
Author (Corporate):
European Medicines Agency
Series Details:
Press Release
EMA/CHMP/123373/2012 (17.2.12)
Published:
17/02/2012 (Last update: 17/02/2012)
2012-02-17
Press Release: European Medicines Agency recommends conditional approval of Pixuvri (pixantrone) for relapsed or refractory aggressive non-Hodgkin’s B-cell lymphoma
Author (Corporate):
European Medicines Agency
Series Details:
Press Release
EMA/CHMP/121961/2012 (17.2.12)
Published:
17/02/2012 (Last update: 17/02/2012)
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