Values and Quality Policies

Our company values;

  • Ethical
  • Scientific
  • Integrity
  • Accessibility
  • Continuous Education and Improvement
  • Respect For Patient and Family Rights
  • Equity
  • Internal and external customer satisfaction

Our Quality Policies:

  • Ensure our team to adopt our mission and vision,
  • Meeting the expectations of our employees and our customers,
  • Improve our processes continuously,
  • Providing high standard service quality.

General Data Protection Regulation (GDPR) and Information Security Commitment

As of the 25th of May 2018, the European Directive 95/46/EC on “the protection of individuals with regard to the processing of personal data and on the free movement of such data” has been replaced by the new General Data Protection Regulation (GDPR). As we are a CRO collection data on behalf of our clients inside and outside of EU, we comply with the requirements of the GPDR and also the requirements of ISO:27001 as a company certified with ISO:27001. Our commitment is as follows:

On behalf of our company, Klinar CRO, in order to keep information security at the highest level in the field of our support services in clinical researches we operate as;

a) Confidentiality: Where information is only accessible to authorized persons,
b) Integrity: To be aware of the fact that the information is protected and will not be changed from unauthorized alterations,
c) Accessibility: The information is available as needed by authorized users.
We commit that:

• We will not share any information of the people and / or Institutions that we serve with any third parties,
• We will create up-to-date firewalls against the attacks of malicious people who will try to gain unauthorized access to the information of this people and /or Institutions
• We will investigate, measure, report on certain periods for the activities that may risk information security,
• We will ensure that the information requested to public and / or private institutions that we are responsible for is delivered correctly,
• We will endeavor to ensure that the information we collect with the authorities we obtained from public and/or private organizations is accurate
• We will provide you with the correctness and integrity of our company’s information,
• We will take the necessary precautions to prevent such activities, such as not being a source of viruses and malware,
• We comply with all legally defined and determined rules for information security,
• While carrying out our Information Security activities; to maintain our processes by planning what we will do, what resources we will get, who will be responsible, when it will be completed, and how we will evaluate the results.
• We comply with ISO 27001: 2013 Standard requirements, legal statutory requirements and other conditions, customer requirements;
Klinar CRO’s has notified its information security policy to the organization and related parties. Information Security Policy is available as written information.

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.