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Number of documents matching the search criteria: 41873
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Document reference numberResponsible DGDate of publication
C(2019)3916/- SANTE (DG Health and Food Safety) 20/05/2019
Commission implementing Decision
DURCHFÜHRUNGSBESCHLUSS DER KOMMISSION über die Änderung der mit der Entscheidung K(2004)2080 erteilten Zulassung des Humanarzneimittels „TachoSil - Fibrinogen vom Menschen / Thrombin vom Menschen“
C(2019)3915/F1 SANTE (DG Health and Food Safety) 21/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION transferring and amending the marketing authorisation granted by Decision C(96)1689(final) for "Bondronat - Ibandronic acid", a medicinal product for human use
C(2019)3915/- SANTE (DG Health and Food Safety) 20/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION transferring and amending the marketing authorisation granted by Decision C(96)1689(final) for "Bondronat - Ibandronic acid", a medicinal product for human use
C(2019)3914/F1 SANTE (DG Health and Food Safety) 21/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION amending the marketing authorisation granted by Decision C(2016)4397(final) for “Epclusa - sofosbuvir/velpatasvir”, a medicinal product for human use
C(2019)3914/- SANTE (DG Health and Food Safety) 20/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION amending the marketing authorisation granted by Decision C(2016)4397(final) for “Epclusa - sofosbuvir/velpatasvir”, a medicinal product for human use
C(2019)3913/F1 SANTE (DG Health and Food Safety) 21/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION amending the marketing authorisation granted by Decision C(2008)8006 for “Kuvan - sapropterin dihydrochloride”, an orphan medicinal product for human use
C(2019)3913/- SANTE (DG Health and Food Safety) 20/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION amending the marketing authorisation granted by Decision C(2008)8006 for “Kuvan - sapropterin dihydrochloride”, an orphan medicinal product for human use
C(2019)3912/F1 SANTE (DG Health and Food Safety) 21/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION concerning, in the framework of Article 35 of Directive 2001/82/EC of the European Parliament and of the Council, the marketing authorisations for veterinary medicinal products containing 50 mg closantel per ml (as a single active substance) presented as solutions for injection for subcutaneous use in sheep
C(2019)3912/- SANTE (DG Health and Food Safety) 20/05/2019
Commission implementing Decision
COMMISSION IMPLEMENTING DECISION concerning, in the framework of Article 35 of Directive 2001/82/EC of the European Parliament and of the Council, the marketing authorisations for veterinary medicinal products containing 50 mg closantel per ml (as a single active substance) presented as solutions for injection for subcutaneous use in sheep
C(2019)3911/F1 SANTE (DG Health and Food Safety) 20/05/2019
Commission implementing Decision
DURCHFÜHRUNGSBESCHLUSS DER KOMMISSION über die Erteilung einer Zulassung für das Tierarzneimittel "Baycox Iron - Toltrazuril / Gleptoferron" gemäß der Verordnung (EG) Nr. 726/2004 des Europäischen Parlaments und des Rates

Number of documents matching the search criteria: 41873
(Showing page 2 of 4188)