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

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

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