Individual Consulting
- Trial planning, trial preparation and conduct
- Project specific study documents
- Submission to Cantonal Ethical Committee (IRB), Swissmedic and other regulatory authorities
- Risk level determination
- Regulatory issues
Trial Files / Study Protocol Review
- Review of trial documents
- Support with creation, editing and revision
Document Templates
Provision of various document templates:
Study Protocol, amendments, Investigators Brochure etc.
(Requests to CTC-RA@usz.ch)
