ACT EU multi-stakeholder platform kick-off workshop, European Medicines Agency and online, day 1: 13:00 - 18:30, day 2: 08:30 - 13:30, Amsterdam time (CEST), from 22/06/2023 to 23/06/2023

ACT EU multi-stakeholder platform kick-off workshop, European Medicines Agency and online, day 1: 13:00 - 18:30, day 2: 08:30 - 13:30, Amsterdam time (CEST), from 22/06/2023 to 23/06/2023

Opinion/decision on a Paediatric investigation plan (PIP): Fusion protein composed of the first 2 immunoglobulin (Ig)-like domains of the human ROBO2 fused to human IgG1 Fc (PF-06730512), decision type: , therapeutic area: , PIP number: P/0431/2022

Opinion/decision on a Paediatric investigation plan (PIP): Fusion protein composed of the first 2 immunoglobulin (Ig)-like domains of the human ROBO2 fused to human IgG1 Fc (PF-06730512), decision type: , therapeutic area: , PIP number: P/0431/2022

Human medicines European public assessment report (EPAR): Cholib, fenofibrate,simvastatin, Dyslipidemias, Date of authorisation: 26/08/2013, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Cholib, fenofibrate,simvastatin, Dyslipidemias, Date of authorisation: 26/08/2013, Revision: 16, Status: Authorised

Human medicines European public assessment report (EPAR): Zarzio, filgrastim, Neutropenia;Hematopoietic Stem Cell Transplantation;Cancer, Date of authorisation: 06/02/2009, Revision: 24, Status: Authorised

Human medicines European public assessment report (EPAR): Zarzio, filgrastim, Neutropenia;Hematopoietic Stem Cell Transplantation;Cancer, Date of authorisation: 06/02/2009, Revision: 24, Status: Authorised

Human medicines European public assessment report (EPAR): Adrovance, alendronic acid,colecalciferol, Osteoporosis, Postmenopausal, Date of authorisation: 04/01/2007, Revision: 25, Status: Authorised

Human medicines European public assessment report (EPAR): Adrovance, alendronic acid,colecalciferol, Osteoporosis, Postmenopausal, Date of authorisation: 04/01/2007, Revision: 25, Status: Authorised

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