Clinical Science
Clinical development with vision - individual solutions for your research.
Our experienced clinical development experts will guide you through all phases of your clinical trial with individually tailored strategies - from the project idea to submission to the regulatory authorities. Thanks to our extensive expertise in multicenter studies and oncology research (national and international), we offer end-to-end support for your study project. After submission, our Clinical Operations team ensures that your study runs smoothly, ensuring successful implementation and meaningful results.
Our services
- Collaboration with investigators to develop innovative study concepts
- Feasibility analyses and selection of suitable study centers (Site Feasibility & Selection)
- Technical support with protocol preparation, budget planning and contract coordination
- Organization of logistics for investigational medicinal products (IMP) or medical devices
- Management of the study team during planning and submission to
ethics committees and authorities
Research collaborations - achieving more together
Translational Research
Partnerships with leading universities and laboratories provide access to cutting-edge technologies, pathology analysis and translational research units - for precise response assessments and high-quality data.
Industry cooperations
In close cooperation with pharmaceutical companies and medical device manufacturers, we accelerate the development of innovative therapies and help to bring new active substances and devices to Switzerland as part of Investigator-Initiated Trials (IITs).
Consulting Services - from the idea to the study protocol ready for approval
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Roch-Philippe Charles
Chief Scientific Officer
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Katrin Eckhardt
Head of Clinical Project Development
Consulting services
Would you like to develop your research vision professionally? Our experienced team will support you in designing and developing a study protocol ready for submission.
Contact us - we look forward to hearing from you.