Training Resources
EMA has developed a series of training videos entitled 'EMA basics'.
Together with the videos, EMA provides the presentation slides and related documents.
Workshops
For information on recent EMA workshops of particular relevance to healthcare professionals, or where they have participated as speakers, see:
- EMA multi-stakeholder workshop on psychedelics – Towards an EU regulatory framework (16-17/04/2024)
- HMA/EMA multi-stakeholder workshop on shortages (01/03/2023)
- ACT EU multi-stakeholder platform kick-off workshop (22/06/2023)
- ACT EU PA04 - Multi-stakeholder Workshop on ICH E6 R3 - Public Consultation (13/07/2023)
- Joint Heads of Medicines Agencies (HMA)/European Medicines Agency (EMA) AI workshop – Smart regulation in a rapidly evolving world (20/11/2023)
- Workshop on generating clinical evidence for treatment and prevention options for long-COVID / post-acute sequelae condition (PASC) (17/11/2023)
- ACT EU PA08 multi-stakeholder methodology workshop (23/11/2023)
- Multistakeholder workshop on EMA’s extended mandate (01/04/2022)
- Protection of personal data and commercially confidential information (CCI) for documents uploaded and published in the Clinical Trials Information System (CTIS): Workshop on draft guidance (14/07/2022)
- Multi-stakeholder workshop: Patient experience data in medicines development and regulatory decision-making (21/09/2022)
- Workshop on the application of the General Data Protection Regulation (GDPR) in the area of health and Secondary Use of Data for Medicines and Public Health Purposes(23/09/2020)
- Workshop on benefit-risk of medicines used during pregnancy and breastfeeding(22/09/2020)
- ICH E6(R3) good clinical practice workshop with Patients' and Consumers' (PCWP) and Healthcare Professionals' (HCPWP) Working Parties(03/06/2020)
- PCWP and HCPWP joint meeting: info session on antimicrobial resistance(19/09/2017)
- PCWP) and HCPW joint workshop on personalised medicines(14/03/2017)