Clinical studies are commissioned and sponsored by national or international pharmaceutical companies.
Their main objective is to evaluate the efficacy and safety of newly discovered drugs, medical devices
or methods of treatment Key benefits of the research are:
- Free access to the latest treatments and new drugs
- The highest standards of medical care
- Free laboratory testing and medical diagnostics
- Constant attendance by the investigator (medical specialist)
Each participant in a research project first goes through a screening. This is the first phase of the
study during which the investigator qualifies the subject to the next periods of the study Each patient
must meet all entrance criteria to start treatment phase of the trial.
Before entering the study, each patient is fully informed (by Investigator and in written) about study
drugs, potential risk, potential benefit, visits schedule, medical procedures, etc. Then patient is
requested to sign a form (informed consent for=ICF) acknowledging that he was told of these risks,
understands them, and consents to the treatment. Agreement may be withdrawn at any time during the
clinical research without giving any reasons and without any consequences for patient.
Your health and safety are a priority for us. All the studies carried out in accordance with the
principles of Good Clinical Practice (GCP) regulations.
