Our Service
I.D.E.A. Ltd combines pharmaceutical industry knowledge with practical experience to bring you a comprehensive service, which includes all the know-how and methodology needed to cover your requirements for the legal and technical processing of clinical trial research and drug development in Europe.
In addition to EU Legal Representation of non-EU Sponsor, we offer a range of clinical, regulatory, and project management services to support the development of your projects within the EU. Moreover, the specialists of this company have extensive experience with the EMEA, US FDA and local regulatory agencies.
The staff of I.D.E.A. Ltd. have been trained on the new regulatory requirements and have extensive experience in regulatory issues, ranging from clinical trial applications to MAA dossier preparation and submission.
Location
The offices of I.D.E.A. Ltd. are located in Cambridge, UK and Munich, Germany.
I.D.E.A. has access to all European regulatory bodies directly or through the European offices of Harrison Clinical Research.
Specialised Services
I.D.E.A. Ltd specialises in assisting Sponsors based in the USA, Japan, Israel, South Africa, India and Australasia with conducting their EU clinical trials in compliance with EU Legislation and Guidelines.