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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.