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 1: Clinical Trials Regulation Overview, Objectives and why the Replacement of EU Directive is needed

Session Chair(s)

Steffen Thirstrup, MD, PhD

Chief Medical Officer

European Medicines Agency, Netherlands

Clinical Trials Regulation Overview and the New Process

Speaker(s)

Key changes from Directive to Regulation and Associated Challenges

Massimiliano Sarra, PhD, MPH

Italian Medicine Agency (AIFA), Italy

Permanent official and CTFG Secretary