Human medicines European public assessment report (EPAR): Simulect, basiliximab, Graft Rejection;Kidney Transplantation, Date of authorisation: 09/10/1998, Revision: 28, Status: Authorised

Human medicines European public assessment report (EPAR): Simulect, basiliximab, Graft Rejection;Kidney Transplantation, Date of authorisation: 09/10/1998, Revision: 28, Status: Authorised

Human medicines European public assessment report (EPAR): Byfavo, remimazolam, Conscious Sedation, Date of authorisation: 26/03/2021, Revision: 6, Status: Authorised

Human medicines European public assessment report (EPAR): Byfavo, remimazolam, Conscious Sedation, Date of authorisation: 26/03/2021, Revision: 6, Status: Authorised

Opinion/decision on a Paediatric investigation plan (PIP): 4-[3-(Methylsulfonyl)phenyl]-1-propylpiperidine x HC1 (pridopidine hydrochloride), decision type: , therapeutic area: , PIP number: P/0546/2022

Opinion/decision on a Paediatric investigation plan (PIP): 4-[3-(Methylsulfonyl)phenyl]-1-propylpiperidine x HC1 (pridopidine hydrochloride), decision type: , therapeutic area: , PIP number: P/0546/2022

Reflection paper on ethical and good-clinical-practice aspects of clinical trials of medicinal products for human use conducted outside of the European Union (EU) / European Economic Area and submitted in marketing-autho...

Reflection paper on ethical and good-clinical-practice aspects of clinical trials of medicinal products for human use conducted outside of the European Union (EU) / European Economic Area and submitted in marketing-autho...

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