European Union clinical trials portal and Union database: meeting with stakeholders
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In the new European Union (EU) Regulation on clinical trials, the Agency has been made responsible for developing and maintaining the IT platforms that will support sponsors and EU Member State representatives carry out their respective roles related to the submission, assessment and supervision of clinical trials in the EU. The EU clinical trials portal and Union database meetings with stakeholders will be held on various dates to inform the design and development of the systems.Registration by invitation only.