Joint EC/HMA/EMA multi-stakeholder workshop on pharmacogenomics

Czech is available via eTranslation, the European Commission's machine translation service.

Translate to Czech | Important information about machine translation

Date

, -

Místo konání

Online
European Medicines Agency, Amsterdam, the Netherlands
Live broadcast

Event summary

The European Commission (EC), the Heads of Medicines Agencies (HMA) and the European Medicines Agency (EMA) are organising a multi-stakeholder hybrid workshop on Pharmacogenomics at EMA in Amsterdam.

The objectives of the workshop are to:

  • identify priority areas for additional regulatory action to promote the clinical implementation of pharmacogenomics;
  • discuss how medicines regulators can facilitate the uptake of genomics by national healthcare systems;
  • discuss how to leverage genomic data linked to real-world data sources with examples of current studies using such data;
  • discuss how to increase the regulatory impact of EU-funded projects in personalised medicine.

The outcome of the workshop will inform a roadmap towards the clinical implementation of pharmacogenomics in Europe.

Virtual participation to the event is open to all stakeholders. Prior registration will be required. In-person participation will be confirmed by invitation only.

The event will be broadcast and recorded, and the recording will be made available on the EMA event page a few weeks after the event.

Registration

Registration is closed

Documents

Video recording

Share this page