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Clinical Trial Regulation Conference

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

Session Chair(s)

Anne  De Bock

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)

Noemi  Manent

The EU Portal and Database: What to Expect. Demo of the draft Portal.

Noemi Manent

  • Scientific Administrator, Compliance and Inspection
  • European Medicines Agency, Netherlands
John  Poland, PhD

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

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+41 61 225 51 51


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+41 61 225 51 49