Organisation
Consistent service is assured by assigning an EU Regulatory Affairs Executive to manage each project. Your EU RAE will remain your main contact for the duration of the trial, offering guidance, keeping you informed of any communications with the authorities or changes in European legislation that may impact on your clinical trial.
I.D.E.A. can represent you in all 27 countries of the European Union
Austria
Belgium
Bulgaria
Cyprus
Czech Rep.
Denmark
Estonia
Finland
France
Germany
Greece
Hungary
Ireland
Italy
Latvia
Lithuania
Luxembourg
Malta
Netherlands
Poland
Portugal
Romania
Slovakia
Slovenia
Spain
Sweden
United Kingdom