Where Execution Meets Excellence
Clinical trial management.
Reliable project management.
Where Execution Meets Excellence
Clinical trial management.
Reliable project management.
The Perfect Framework for Your Research.
Our goal is to create the perfect environment for your project. Our experience in the vascular medicine field enables us to manage your clinical research on the highest standards.
You remain in full control about our extent of integration into your project. We adapt to your wishes and guide you through planning, implementation, review or evaluation of your trial. And of course, we can also assist you every step of the way.
Full service clinical trial operations with us means every relevant task from selecting the right partners and hospitals, managing submission to Ethics Committees through to writing the final study report. Everything that helps you to focus on what matters — research with excellence.
Our CRO Project Management services
- Support in preparing the Clinical Investigation Plan
- Vendor Management: involvement of analytical laboratories, statistical services, data manager, consultant specialists, insurance companies
- Site Selection and Site Agreement Handling
- Study document preparation and maintenance, like patient informed consent form, CRF, operational manuals and Trial Master File
- Submissions to Ethics Committees and Competent Authorities and relevant reporting
- Registration in public registers
- Organisation of investigator meetings
Where Execution Meets Excellence
Seamless Monitoring.
Smart On-Site-Management.
Where Execution Meets Excellence
Seamless Monitoring.
Smart On-Site-Management.
We Are Where You Need Us To Be
Always right by your side – or wherever you need us to be. As a centralized hub between scientists, doctors, trial sites, sponsors and partners we overlook entire projects from a birds eye view. Our CRAs are on site, constantly monitor crucial process steps within your study. Fair, critical and reliable.
Our CRA Services
- Preparation and review of investigator site file (ISF)
- Site initiation visits (SIV) with protocol and (e)CRF training
- Site monitoring visits (SMV) to verify the protocol and GCP compliant trial conduct, source data verification and documentation of adverse events (AEs)
- Close-out visits (COV)
- Site support during study conduct
