Clinical Trial Regulation Information Day for CEE Countries

Are Central and Eastern European Union member states ready to implement the new EU Clinical Trial Regulation (536/2014)? This information day provides a platform for discussion about the status of the implementation and further compliance with the new Regulation, as well as the associated legislation in the region.

戻る Agenda

Session 2: Industry Preparedness and View: Panel Discussion

Session Chair(s)

Catalina Sarbu

Director Clinical Operations, PAREXEL International Romania s.r.l.

President of the Romanian CRO Association (ASSCRC) , Romania

Industry Preparedness for the Implementation of CT Regulation