Menu Back toSESSION-7-KEY-ELEMENTS-OF-CT-DATA-TRANSPARENCY-IN-THE-EU

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 7: KEY ELEMENTS OF CT DATA TRANSPARENCY IN THE EU

Session Chair(s)

Matthias  Zerm, PhD

Matthias Zerm, PhD

  • Lead Expert, Clinical Trial Disclosure and R&D Processes
  • Merz Pharmaceuticals GmbH, Germany

Get an overview of how transparency is reflected in all regulations and policies - EU CTReg, Paediatric Regulation,Data Protection Regulation and Policy 70 – and how it all comes together.

Speaker(s)

Emma  Du Four, MBA

Implementation of the Clinical Trial Disclosure Provisions of the CTReg

Emma Du Four, MBA

  • Head of International Regulatory Policy
  • Abbvie, United Kingdom
Christian  Fulda

Mandatory Disclosure of Clinical data in the EU

Christian Fulda

  • Lawyer
  • Jones Day, Germany

Contact us

 Registration Questions

Send Email
+41 61 225 51 51


Agenda and Logistics Questions

Send Email
+41 61 225 51 49