Our Service
This service company combines the pharmaceutical industry knowledge with the 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.
We offer a range of activities and services to support your clinical, regulatory, and project management issues related to the development of your projects in the EU. Moreover, the specialists of this company have extensive experience with the EMEA and other regulatory agencies.
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.
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.
Particular help
I.D.E.A. Ltd. is set-up to be of particular help to sponsors in the countries Japan, USA, Israel, South Africa, India and Australasia.