This conference provides a forum for information exchange and discussion on conceptual and practical questions about critical issues affecting sponsors and Member States regarding the implemention the regulation.
SESSION 6: EU PORTAL & DATABASE
Anne De Bock
Sr Regional Director
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.
The EU Portal and Database: What to Expect.
Demo of the draft Portal.
Scientific Administrator, Compliance and Inspection
European Medicines Agency, Netherlands
A stakeholder's perspective of the EU clinical trials portal and database
John Poland, PhD
Regulatory Affairs Consultant
Association of Clinical Research Organizations (ACRO), United Kingdom