Pharming Group recibe evaluación acelerada en Europa para leniolisib para el tratamiento de la inmunodeficiencia poco común, APDS ...Middle East

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Pharming Group recibe evaluación acelerada en Europa para leniolisib para el tratamiento de la inmunodeficiencia poco común, APDS
source : PR Newswire ( Middle East ) () 41
La evaluación acelerada de la EMA reduce el período de revisión para leniolisib de 210 a 150 días Pharming avanza para presentar su solicitud de autorización de comercialización para leniolisib en el segundo semestre de 2022 LEIDEN, Países Bajos, 3 de agosto de 2022 /PRNewswire/ --...

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