Industry Update webinar on Regulatory Procedure Management for Product Lifecycle Management on IRI, Online, European Medicines Agency, Amsterdam, the Netherlands, from 13 June 2024, 10:00 (CEST) to 13 June 2024, 11:30 (CEST)

Network Update webinar on Regulatory Procedure Management for Product Lifecycle Management on IRIS, Online, European Medicines Agency, Amsterdam, the Netherlands, from 18 June 2024, 10:00 (CEST) to 18 June 2024, 11:30 (CEST)

Annex II to the call for proposals - Vendor financial identification form

Committee for Medicinal Products for Human Use (CHMP): 19-22 February 2024, European Medicines Agency, Amsterdam, the Netherlands, from 19 February 2024 to 22 February 2024

SPOR Status Update, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 10 July 2024, 10:00 (CEST) to 10 July 2024, 12:30 (CEST)

Timetable: Safety signal - Assessment of responses to request for supplementary information (RSI)

Timetable: Safety signal - Assessment of responses to request for supplementary information (RSI) - ATMP

Timetable: Post-authorisation measure (PAM) Paediatric art. 46 submission - ATMP

Timetable: Post-authorisation measure (PAM) assessed by CHMP

Timetable: Post-authorisation measures (PAMs) assessed by PRAC - ATMP