About Us

Klinar CRO was established in January 2009 as an Optimum CRO enterprise for the international trials conducted in Turkey. Optimum CRO is one of the first CROs established in Turkey in 2000. In September 2018, we decided to merge our companies back together again in order to be stronger in our projects we are carrying out under the name of Klinar CRO.

Klinar CRO has staff including CRAs, PMs, QC, SCs and data management units which are located in the main office based in Ankara, the capital city of Turkey.

With its high development rate, Klinar CRO is one of the leading and experienced foundations for conduct, organization and improvement of clinical researches in Turkey.

Currently, KlinAR CRO 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”.

KlinAR CRO also has additional quality certificate as ISO:27001 Data Safety and Integrity Certificate.

In addition to the main office based in Ankara, depending on the project needs, KlinAR may provide home based personnel in several cities.

With Optimum CRO’s leading experience KlinAR CRO and its team has a deep experience over the clinical trials of different phases and post marketing surveillance studies.

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 .

Klinar CRO has comprehensive and detailed SOPs to guide and train all staff, to ensure operations to be carried out in compliance with ICH/GCP and regulations to fulfill the sponsor companies’ requests and requirements.In addition, in Klinar CRO‘s project management system, it is always possible to work with sponsor companies’ SOPs.

With our extensive background in this field, our specialized team and with the philosophy of continous improvement, we are ensuring to provide the services you need with the excellent process.

Klinar Company Brochure

Designing and Regulatory Affairs

Monitoring and Project Management

Training Services

Data Management and Analysis

Translation and Publication

Safety Management

Clinical Drug Studies

Klinar CRO has its clinical drug studies history varying from phase I to IV studies.

Observational Studies

Klinar is working on late phase studies such as pharmacovigilance follow-up studies, post-marketing survelliance studies, large scale registry studies, practice pattern studies.

Site Management Organization

Klinar also offers solutions for managing your clinical trials inside level.

Compassionate Use

Klinar CRO has the ability to manage compassionate use studies both in project level and patient level.

Patient Follow-Up Studies

Klinar offers private solutions for tracking systems for your products requiring special follow-up in terms of pharmacovigilance, patient call management by using customer oriented electronic systems and call centers.

Medical Device Studies

Medical device studies for in vivo and in vitro medical devices with or without CE mark is within Klinar's expertise.

Start-Up Activities

Feasibility assesments and start-up expertise sharing for new clients requesting to know more about Turkey's infrastructure is available in Klinar's expertise.

Regulatory Submissions Support

Klinar can support you for all your regulatory submissions in terms of ethics committee and regulatory authority submissions including contract management.

We Have Great Skills

Klinar CRO has a wide range of experience in different therapeutic areas.
Different types of trials such as; Clinical Trials, Post Marketing Trials, Site Management Organization, Electronic Data Capture, ATMP studies, Medical Device Studies and Compassionate Use are being conducted by Klinar CRO.

Clinical Drug Studies
Observation Studies
Other Studies

Get Your Quote or Call: +(90) (312)-447-0274

For clear strategies for your project with flexible, professional, proactive teamwork with competitive costs.