I.D.E.A. Ltd combines pharmaceutical industry knowledge with practical experience to bring you a comprehensive Legal Representative 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.
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.
The sponsor may also choose from our range of service options to create a customized package designed to help you fully comply with European requirements:
- Regulatory Affairs Advice and Services
- Organisation of Liability Insurance
- Pharmacovigilance Advice and Service
- Medical Monitoring
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.
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.