Clinical Research Ward

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.

Consulting:

• Budgeting, study management and conduct of clinical trials.

Services:

• 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.

Reporting:

• Support with the creation of study reports (progress, safety, final) 

We operate a fully equipped clinical research ward for conducting Phase I, II and III clinical trials and further research projects. Research projects are lead by investigators of the University Hospital Zurich. 

Clinical Research Ward - Services:

• Comprehensive support to reach and maintain highest quality standards according to Good Clinical Practice (ICH-GCP) and in compliance with regulatory requirements.
• Conduct of clinical trials by qualified specialist staff in compliance with international guidelines (ICH-GCP) and legal requirements
• The Clinical Research Ward operates an integrated ward with 8 treatment places or hospital beds
• Logistics and drug randomization