Regulatory Affairs

​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)​

Flyer (PDF)
​ 

 


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