Phase I clinical trials of drugs the preclinical studies of which have been completed have been performed both in healthy volunteers and in patient volunteers in our clinic.  For this purpose, the researchers who will take part in the studies in our clinic must fulfill the following conditions:

     - The research to be carried out needs to be approved by the Ethics Committee and the Ministry of Health.

     - The researchers who will participate in the studies must be assigned to the Hakan Çetinsaya Good Clinical Practice and Research Center during the research period.

     - In accordance with the relevant Regulation, phase I clinical investigations must be performed by pharmacologists (as principal investigator) who have the title of MD. Researchers from other departments who will participate in research can work as co-investigators.

     - It is necessary to draw up contracts before the research between our clinic and private or public organizations that are sponsor for the research.