The Perfect Framework for Your Research.

Our goal is to create the perfect environment for your project. Our experience in the field of vascular medicine enables us to manage your clinical research to the highest standards.

You determine the extent of our integration into your project. We adapt to your wishes and guide you through planning, implementation, review or evaluation of your trial. If you wish, we can assist you every step of the way.

Full service clinical trial operations with us include every relevant task from selecting the right partners and hospitals, managing submission to Ethics Committees through to writing the final study report. We cover everything that helps you 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, such as 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