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Líon na gcáipéisí a fhreagraíonn do critéir chuardaigh sin: 36842
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Uimhir tagartha an doiciméidAn Ard-Stiúrthóireacht a bhfuil an cúram sin uirthiDáta foilsithe
C(2018)6290/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
DURCHFÜHRUNGSBESCHLUSS DER KOMMISSION über die Erteilung einer Zulassung für das Humanarzneimittel "Udenyca - Pegfilgrastim" gemäß der Verordnung (EG) Nr. 726/2004 des Europäischen Parlaments und des Rates
C(2018)6289/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION granting marketing authorisation under Regulation (EC) No 726/2004 of the European Parliament and of the Council for "Imfinzi - durvalumab", a medicinal product for human use
C(2018)6288/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION granting marketing authorisation under Regulation (EC) No 726/2004 of the European Parliament and of the Council for "Pelgraz - pegfilgrastim", a medicinal product for human use
C(2018)6286/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION amending the marketing authorisation granted by Decision C(2015)3647(final) for “Voriconazole Hikma - voriconazole”, a medicinal product for human use
C(2018)6285/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION transferring and amending the marketing authorisation granted by Decision C(2005)811 for "Zonegran - zonisamide", a medicinal product for human use
C(2018)6283/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION on the transfer of the marketing authorisation granted by Decision C(2007)177 for "Inovelon - Rufinamide", an orphan medicinal product for human use
C(2018)6282/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION amending the marketing authorisation granted by Decision C(2010)8908 for “Brilique - ticagrelor”, a medicinal product for human use
C(2018)6281/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION renewing and amending the marketing authorisation for the medicinal product for human use "Tivicay - dolutegravir", granted by Decision C(2014)305(final)
C(2018)6280/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION on the transfer of the marketing authorisation granted by Decision C(2012)5340(final) for "Fycompa - Perampanel", a medicinal product for human use
C(2018)6279/- SANTE (AS um Shláinte agus Sábháilteacht Bia) 21/09/2018
Cinneadh cur chun feidhme ón gCoimisiún
COMMISSION IMPLEMENTING DECISION on the transfer of the marketing authorisation granted by Decision C(2013)9830(final) for "Opsumit - macitentan", an orphan medicinal product for human use

Líon na gcáipéisí a fhreagraíonn do critéir chuardaigh sin: 36842
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