To initiate cooperation, a tripartite agreement between IKEM, the PI, and the sponsor (or CRO) is always required. A non-disclosure agreement shall also be attached as part of the contract.
Electronic signing of contract via a qualified certificate is accepted. More information can be found in Pravidla elektronického podepisování dokumentů prostřednictvím kvalifikovaných certifikátů v IKEM.
If IKEM laboratories are used, this fact shall be addressed in the contract. More detailed information about the laboratories can be found in Všeobecné informace, or you can contact the coordinator assigned to your clinical trial or clinical evaluation of medical devices. In the case of the loan of any equipment, it is necessary to conclude a separate loan agreement before the start of the clinical trial or clinical evaluation of medical devices itself. If an additional loan occurs, the documentation must be processed and the loan agreement concluded before the equipment is delivered to IKEM.
Before concluding a new loan agreement, all previous equipment loan agreements for the given clinical trial or clinical evaluation of medical devices must be terminated/settled.