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Last updated about 5 hours ago
Twelfth Industry Standing Group (ISG) meeting, Online, European Medicines Agency, Amsterdam, the Netherlands, from 28 March 2025, 09:00 (CET) to 28 March 2025, 14:00 (CET)
about 5 hours ago
Twelfth Industry Standing Group (ISG) meeting, Online, European Medicines Agency, Amsterdam, the...
Thirteenth meeting of the industry stakeholder platform on research and development support, European Medicines Agency, Amsterdam, the Netherlands, 2 December 2024
about 5 hours ago
Thirteenth meeting of the industry stakeholder platform on research and development support...
Highlight report - 13th Industry stakeholder platform on research and development support
about 5 hours ago
Highlight report - 13th Industry stakeholder platform on research and development support
Human medicines European public assessment report (EPAR): Roclanda, latanoprost / netarsudil, Date of authorisation: 07/01/2021, Revision: 8, Status: Authorised
about 6 hours ago
Human medicines European public assessment report (EPAR): Roclanda, latanoprost / netarsudil, Date...
Human medicines European public assessment report (EPAR): Ajovy, fremanezumab, Date of authorisation: 28/03/2019, Revision: 13, Status: Authorised
about 6 hours ago
Human medicines European public assessment report (EPAR): Ajovy, fremanezumab, Date of authorisation...
Human medicines European public assessment report (EPAR): SomaKit TOC, edotreotide, Date of authorisation: 08/12/2016, Revision: 21, Status: Authorised
about 7 hours ago
Human medicines European public assessment report (EPAR): SomaKit TOC, edotreotide, Date of...
Human medicines European public assessment report (EPAR): Stoboclo, denosumab, Date of authorisation: 14/02/2025, Status: Authorised
about 7 hours ago
Human medicines European public assessment report (EPAR): Stoboclo, denosumab, Date of authorisation...
Human medicines European public assessment report (EPAR): Avtozma, tocilizumab, Date of authorisation: 14/02/2025, Status: Authorised
about 8 hours 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
about 8 hours 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
about 8 hours ago
Human medicines European public assessment report (EPAR): Rivastigmine Hexal, rivastigmine, Date of...