Sponsors / CRO Responsibilities

Clinical trials are to be performed on the basis of two independent agreements when one agreement is to be concluded between the Sponsor and the University Hospital Olomouc and Principal Investigator. The second one between the Sponsor and Principal Investigator (eventually between the Sponsor and the Study team).

Administrator of the Department of Science and Clinical Research is the primary contact for CRO or a Pharmaceutical Company willing to conduct a clinical study in the University Hospital Olomouc when full details such as three-party agreements, study protocol and other documents are to be provided.

Administrator then executes the following documents:

• General information regarding the clinical trial in question
• Contract Proposal
• Pharmacy Form
• Other documents necessary for internal purposes