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Our team is composed of highly qualified experts with many years of experience who successfully
manage any (Initiate, manage, monitor) stage of clinical (Phase I-IV) and device trials within their
competence.

We cooperate with more than 20 medical institutions across Georgia, where we have sites. We are
constantly working to add new sites.

according to the current legislation, local ethic committee (LEC) are provided at each site, which leads to
timely review of cases and issuance of appropriate conclusions.

Under current legislation,  the research approval are usually issued within 30 days of application by regulation agency. However, in
the case of a gap in the documentation, the regulatory may ask additional questions, which will
extend the authorisation for only 30 days. 

We cooperate with family doctors and outpatient clinics across the country, so the number of patients
involved is not limited to patients of a specific PI or one specific clinic.