Events

22 Jun 2026

Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting inthe EU: Hands-on training course using the EudraVigilance System

Online

Start date: 22 June 2026

End date: 26 June 2026

EventHumanClinical trials

22 Jun 2026

Committee for Medicinal Products for Human Use (CHMP): 22-25 June 2026

European Medicines Agency, Amsterdam, the Netherlands

Start date: 22 June 2026

End date: 25 June 2026

EventHumanMedicines

22 Jun 2026

eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) training course - June 2026

Online

Start date: 22 June 2026, 09:00 (CEST)

End date: 24 June 2026, 13:30 (CEST)

EventHumanRegulatory and procedural guidance

22 Jun 2026

Shortage prevention plan (SPP) workshop

Online

Start date: 22 June 2026, 10:30 (CEST)

End date: 22 June 2026, 12:30 (CEST)

EventHumanMedicine shortages

23 Jun 2026

Paediatric Committee (PDCO): 23-26 June 2026

Online

European Medicines Agency, Amsterdam, the Netherlands

Start date: 23 June 2026

End date: 26 June 2026

EventHumanPaediatrics

24 Jun 2026

Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) - June 2026

Online

European Medicines Agency, Amsterdam, the Netherlands

Start date: 24 June 2026, 10:00 (CEST)

End date: 24 June 2026, 12:00 (CEST)

EventHumanMedicine shortages

25 Jun 2026

Quarterly System Demo - Q2 2026

Online

European Medicines Agency, Amsterdam, the Netherlands

Live broadcast

Start date: 25 June 2026, 09:00 (CEST)

End date: 25 June 2026, 12:40 (CEST)

EventCorporate

25 Jun 2026

PMS Q&A Clinic on Product User Interface (PUI) and Application Programming Interface (API) – June 2026

Online

Start date: 25 June 2026, 09:30 (CEST)

End date: 25 June 2026, 10:30 (CEST)

EventHumanMedicines

29 Jun 2026

17th Industry Standing Group (ISG) meeting

Online

Start date: 29 June 2026, 09:30 (CEST)

End date: 29 June 2026, 13:10 (CEST)

EventHumanVeterinary

30 Jun 2026

Good manufacturing practice: Multistakeholder workshop on expert contributions to artificial intelligence guidance development (Annex 22)

EMA's Good Manufacturing Practice (GMP) / Good Distribution Practice (GDP) Inspectors Working Group is organising a two-day workshop to help shape a risk-based approach to the use of generative artificial intelligence (AI) in medicines manufacturing.

Online

European Medicines Agency, Amsterdam, the Netherlands

Start date: 30 June 2026, 09:00 (CEST)

End date: 1 July 2026, 17:00 (CEST)

EventHumanCompliance and inspectionsRegulatory and procedural guidanceResearch and development

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