You are looking for a trustful partner for your clinical studies? We take care of the strategic planning and the operational implementation.

For the successful implementation of your clinical studies we offer an overall concept from a single source:

• Strategic and operational planning
• Medical advisory
• Documentation
• KOL-management
• Organization of Advisory Boards

for oncology phase I-III studies according to ICH-GCP, the "Declaration of Helsinki" and any local law that may apply. We document the course of the study on an ongoing basis and keep focus on primary study objectives. You will have a comprehensive overview on the actual study site status at any time .

To complement our services we also offer monitoring of clinical studies in Oncology focussing on:

• Optimization of study-related processes at study sites
• First line of contact for principal investigator and site personnel
• Study-specific training for site personnel
• Source data verification and monitoring
• Start-up and close-out visits

If you are interested in our global services for Clinical Research in Oncology we are happy to receive a message from you !