We support clinical researchers of the University Hospital Zurich and of partners in the planning and conducting of clinical trials according to applicable laws and internatonial standards (ICH-GCP). We also conduct clinical research projects with our specialized staff and our infrastructure and logistics.
- Budgeting, study management and conduct of clinical trials.
- Preparation and conduct of clinical trials for academic researchers
- Specialist staff
- Trial facilities
- Conduct of clinical trials in compliance with international guidelines (ICH-GCP) and legal requirements
Study documents & notification to regulatory bodies:
- Support with the creation, preparation and submitting of study documents for the notification to regulatory authorities, in cooperation with the CTC‘s Regulatory Affairs Unit.