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Last updated 10 minutes ago

Human medicines European public assessment report (EPAR): Avtozma, tocilizumab, Date of authorisation: 14/02/2025, Status: Authorised

12 minutes ago

Human medicines European public assessment report (EPAR): Avtozma, tocilizumab, Date of authorisation...

Human medicines European public assessment report (EPAR): Rivastigmine Sandoz, rivastigmine, Date of authorisation: 10/12/2009, Revision: 18, Status: Authorised

14 minutes ago

Human medicines European public assessment report (EPAR): Rivastigmine Sandoz, rivastigmine, Date of...

Human medicines European public assessment report (EPAR): Rivastigmine Hexal, rivastigmine, Date of authorisation: 11/12/2009, Revision: 19, Status: Authorised

22 minutes ago

Human medicines European public assessment report (EPAR): Rivastigmine Hexal, rivastigmine, Date of...

Human medicines European public assessment report (EPAR): Rivastigmine 1 A Pharma, rivastigmine, Date of authorisation: 11/12/2009, Revision: 19, Status: Authorised

32 minutes ago

Human medicines European public assessment report (EPAR): Rivastigmine 1 A Pharma, rivastigmine...

Orphan designation: bexmarilimab Treatment of myelodysplastic syndromes, 25/03/2025 Positive

about 1 hour ago

Orphan designation: bexmarilimab Treatment of myelodysplastic syndromes, 25/03/2025 Positive

Orphan designation: ixodes ricinus contact phase inhibitor Treatment of non-traumatic spontaneous intracerebral haemorrhage, 25/03/2025 Positive

about 2 hours ago

Orphan designation: ixodes ricinus contact phase inhibitor Treatment of non-traumatic spontaneous intracerebral...

Human medicines European public assessment report (EPAR): Rxulti, brexpiprazole, Date of authorisation: 26/07/2018, Revision: 7, Status: Authorised

about 3 hours ago

Human medicines European public assessment report (EPAR): Rxulti, brexpiprazole, Date of authorisation...

Orphan designation: Felzartamab Treatment of in solid organ transplantation, 13/12/2024 Positive

about 3 hours ago

Orphan designation: Felzartamab Treatment of in solid organ transplantation, 13/12/2024 Positive

Orphan designation: deucrictibant monohydrate Treatment of bradykinin-mediated angioedema, 25/03/2025 Positive

about 3 hours ago

Orphan designation: deucrictibant monohydrate Treatment of bradykinin-mediated angioedema, 25/03/2025 Positive

Human medicines European public assessment report (EPAR): Reblozyl, luspatercept, Date of authorisation: 25/06/2020, Revision: 9, Status: Authorised

about 3 hours ago

Human medicines European public assessment report (EPAR): Reblozyl, luspatercept, Date of authorisation...