EU Helps Sponsors To Steer National Fee Requirements Under Clinical Trials Regulation

A working group of EU regulators has developed a comprehensive repository of fee requirements relating to the Clinical Trials Regulation to help sponsors navigate the diverse demands of member states in the European Economic Area.

Clipboard, woman and scientist writing in laboratory for medical research on cancer drug trial. Checklist, investigation and female biologist with clinic protocol development for pharmaceutical study
EU Regulators Want To Increase The Bloc’s Attractiveness For Clinical Trials (Shutterstock)

The EU Clinical Trials Coordination Group (CTCG) has collected in one place the fee requirements prescribed by different member states in the European Economic Area (EEA) pertaining to submissions under the EU Clinical Trials Regulation (CTR).

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