Klinar CRO was established in January 2009 for the international trials conducted in Turkey. Klinar CRO and its team has a deep experience over the clinical trials of different phases and post marketing surveillance studies. KlinAR is one of the leading and experienced foundations for conduct, organization and improvement of clinical researches in Turkey. Currently, KlinAR CRO which is a member of DIA, has become one of the first  certified CRO to be approved by the Ministry of Health in Turkey, working in compliance with the principles of "Guideline For Good Clinical Practices". In addition to the main office based in Ankara, depending on the project needs, KlinAR provides home based personnel in İstanbul and in İzmir. We provide; Regulatory Services (EC and RA (Ministry of Health) Submissions of the trials are performed and followed-up by KlinAR CRO), Clinical Trial Management (Monitoring and Project Management, Site Management Organization, Post-marketing Surveillance Studies), Medical Affairs (project manager of the study and the medical advisor of KlinAR CRO cooperate in the formation of the report ensuring that obtained data is correctly and fully reflected in the report), Data Management (Data Management Unit constructs the study database and performs statistical analysis defined in the protocol), Investigator Meeting Organization, CRF Design, Study Protocol Design, Training Organziation . Clinical Trials, Post Marketing Trials, Site Management Organization, Electronic Data Capture and Compassionate Use are being conducted by KlinAR CRO. Apart from the local and international sponsor companies, KlinAR’s cooperation with Clinical Research Institutions which operate worldwide is in progress.