Clinical Research

We plan and conduct clinical trials throughout Europe. Implementation of GCP as well as observance of any applicable international guidelines is what our services are based on.

CTA (Clinical Trial Authorization)
Planning of Phase I – IV trials
Trial protocol and CRF preparation
Monitoring by an experienced team of scientifically / medically trained CRAs
Project coordination / project management
Biometrical planning and analysis
Preparation of Integrated Final Reports
Investigator Brochures