Events | European Medicines Agency (EMA)

27 Lut. 2025

Training on human variations web-based electronic application form (eAF) functionalities for CAPs and non-CAPs variations

Online

European Medicines Agency, Amsterdam, the Netherlands

Data początkowa: 27 luty 2025, 10:30 (CET)

Data końcowa: 27 luty 2025, 12:30 (CET)

EventHuman

26 Lut. 2025

Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) – February 2025

Online

European Medicines Agency, Amsterdam, the Netherlands

Data początkowa: 26 luty 2025, 10:00 (CET)

Data końcowa: 26 luty 2025, 12:00 (CET)

EventHumanMedicine shortagesMedicines

25 Lut. 2025

Q&A clinic on Product Management Service (PMS) Product User Interface (PUI) and Application Programming Interface (API) - 25 February 2025

Online

European Medicines Agency, Amsterdam, the Netherlands

Data początkowa: 25 luty 2025, 11:00 (CET)

Data końcowa: 25 luty 2025, 12:00 (CET)

EventHumanData on medicines

25 Lut. 2025

European Shortages Monitoring (ESMP) - Question and answer clinic for marketing authorisation holders on shortage reporting via ESMP

Online

European Medicines Agency, Amsterdam, the Netherlands

Live broadcast

Data początkowa: 25 luty 2025, 10:00 (CET)

Data końcowa: 25 luty 2025, 11:00 (CET)

EventHumanMedicine shortages

25 Lut. 2025

Paediatric Committee (PDCO): 25-28 February 2025

Online

European Medicines Agency, Amsterdam, the Netherlands

Data początkowa: 25 luty 2025

Data końcowa: 28 luty 2025

EventHumanPaediatrics

24 Lut. 2025

Webinar on PMS Project Made Easy: Summary of activities and Practical Tips for SMEs

Online

European Medicines Agency, Amsterdam, the Netherlands

Data początkowa: 24 luty 2025, 14:00 (CET)

Data końcowa: 24 luty 2025, 16:00 (CET)

EventHumanSME

24 Lut. 2025

Mandatory use of ISO/ICH E2B(R3) individual case safety reporting in the EU: hands-on training course using the EudraVigilance system

EudraVigilance is the EU's system for managing and analysing information on adverse reactions to medicines which have been authorised or are being studied in clinical trials in the European Economic Area (EEA) and supports the reporting and analysis of suspected adverse reactions originating from clinical trials and the post-authorisation phase of...

Online

Data początkowa: 24 luty 2025

Data końcowa: 28 luty 2025

EventHumanClinical trials

24 Lut. 2025

Committee for Medicinal Products for Human Use (CHMP): 24-27 February 2025

European Medicines Agency, Amsterdam, the Netherlands

Data początkowa: 24 luty 2025

Data końcowa: 27 luty 2025

EventHumanMedicines

19 Lut. 2025

European Shortages Monitoring Platform (ESMP) training on crisis and MSSG-led preparedness reporting for marketing authorisation holders (MAHs)

Online

European Medicines Agency, Amsterdam, the Netherlands

Live broadcast

Data początkowa: 19 luty 2025, 10:00 (CET)

Data końcowa: 19 luty 2025, 12:30 (CET)

EventHumanMedicine shortages

19 Lut. 2025

ACT EU workshop on ICH E6 R3 (principles and Annex 1)

Online

European Medicines Agency, Amsterdam, the Netherlands

Live broadcast

Data początkowa: 19 luty 2025, 09:30 (CET)

Data końcowa: 20 luty 2025, 14:00 (CET)

EventHumanClinical trials