Design, Planning and Execution of multicentre trials to current GCP and ICH EN ISO 14155 guidelines since 1991.
COMPLETE PROJECT ORGANISATION
- Advice in Investigational Site Identification
- Preparation of Study specific documents
- National Competence Authorities and Ethic Committees’ Submissions
- Site & Data Management
- SAE reporting, Amendments, Notifications, Review
- Case Support
- Study Material Logistics & Device Accountability
- On-site Monitoring and Reporting
Our domains – One solution
Cardiovascular
Cerebrovascular
Emergency medicine
oncology diagnostics
