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SESSION 6: EU PORTAL & DATABASE
Session Chair(s)
Anne De Bock
Sr Regional Director
AstraZeneca, Belgium
What is the status quo and what can you expect to happen in 2017? This session will answer these questions in form of high-level presentations followed by a panel discussion that focuses on the learnings so far from user-acceptance testing.
Speaker(s)
The EU Portal and Database: What to Expect. Demo of the draft Portal.
Noemie Manent, PharmD
European Medicines Agency, Netherlands
TDA-CTT Operations Workstream Lead
A stakeholder's perspective of the EU clinical trials portal and database
John Poland, PhD
Association of Clinical Research Organizations (ACRO), United Kingdom
Regulatory Affairs Consultant
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