Multi-stakeholder workshop on the guideline on clinical investigation of medicinal products in the treatment of epileptic disorders, Online, from 29/01/2024 to 29/01/2024

Multi-stakeholder workshop on the guideline on clinical investigation of medicinal products in the treatment of epileptic disorders, Online, from 29/01/2024 to 29/01/2024

Human medicines European public assessment report (EPAR): Pregabalin Sandoz, pregabalin, Anxiety Disorders;Neuralgia;Epilepsy, Date of authorisation: 19/06/2015, Revision: 17, Status: Authorised

Human medicines European public assessment report (EPAR): Pregabalin Sandoz, pregabalin, Anxiety Disorders;Neuralgia;Epilepsy, Date of authorisation: 19/06/2015, Revision: 17, Status: Authorised

Human medicines European public assessment report (EPAR): Takhzyro, lanadelumab, Angioedemas, Hereditary, Date of authorisation: 22/11/2018, Revision: 12, Status: Authorised

Human medicines European public assessment report (EPAR): Takhzyro, lanadelumab, Angioedemas, Hereditary, Date of authorisation: 22/11/2018, Revision: 12, Status: Authorised

Human medicines European public assessment report (EPAR): Zynrelef, bupivacaine,meloxicam, Pain, Postoperative, Date of authorisation: 24/09/2020, Revision: 3, Status: Withdrawn

Human medicines European public assessment report (EPAR): Zynrelef, bupivacaine,meloxicam, Pain, Postoperative, Date of authorisation: 24/09/2020, Revision: 3, Status: Withdrawn

Human medicines European public assessment report (EPAR): Aqumeldi, Enalapril maleate, Heart Failure, Date of authorisation: 15/11/2023, Status: Authorised

Human medicines European public assessment report (EPAR): Aqumeldi, Enalapril maleate, Heart Failure, Date of authorisation: 15/11/2023, Status: Authorised

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