Data protection and privacy at EMA
Submitted by Anonymous (not verified) on 28 May 2026 - 15:30
Data protection and privacy at EMA
Human medicines European public assessment report (EPAR): Aquipta, atogepant, Date of authorisation: 11/08/2023, Revision: 5, Status: Authorised
Submitted by Anonymous (not verified) on 28 May 2026 - 15:05
Human medicines European public assessment report (EPAR): Aquipta, atogepant, Date of authorisation: 11/08/2023, Revision: 5, Status: Authorised
Champix
Submitted by Anonymous (not verified) on 28 May 2026 - 15:00
Champix
SME Regulation and reports
Submitted by Anonymous (not verified) on 28 May 2026 - 14:55
SME Regulation and reports
20 years supporting small and medium enterprises (SMEs) at EMA report
Submitted by Anonymous (not verified) on 28 May 2026 - 14:45
20 years supporting small and medium enterprises (SMEs) at EMA report
Product Management Service (PMS) information day 2026, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 9 June 2026, 08:45 (CEST) to 9 June 2026, 17:00 (CEST)
Submitted by Anonymous (not verified) on 28 May 2026 - 14:40
Product Management Service (PMS) information day 2026, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 9 June 2026, 08:45 (CEST) to 9 June 2026, 17:00 (CEST)
Human medicines European public assessment report (EPAR): Spikevax (previously COVID-19 Vaccine Moderna), COVID-19 mRNA vaccine, Date of authorisation: 06/01/2021, Revision: 61, Status: Authorised
Submitted by Anonymous (not verified) on 28 May 2026 - 14:36
Human medicines European public assessment report (EPAR): Spikevax (previously COVID-19 Vaccine Moderna), COVID-19 mRNA vaccine, Date of authorisation: 06/01/2021, Revision: 61, Status: Authorised
Product Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 3
Submitted by Anonymous (not verified) on 28 May 2026 - 14:30
Product Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 3
Timetable: Marketing authorisation renewal application - ATMP
Submitted by Anonymous (not verified) on 28 May 2026 - 14:25
Timetable: Marketing authorisation renewal application - ATMP
Timetable: Marketing authorisation renewal application
Submitted by Anonymous (not verified) on 28 May 2026 - 14:20
Timetable: Marketing authorisation renewal application