klinar cro
Klinar CRO is a leading clinical research organization based in Turkey, established in 2009, specializing in the management and organization of clinical trials, post-marketing surveillance, medical device studies, and advanced therapy medicinal product studies. The company is committed to quality, sustainability, and honesty, with certifications including Good Clinical Practices and ISO 27001. Klinar CRO offers a wide range of services including regulatory affairs, monitoring, data management, and training, with extensive experience across various therapeutic areas and phases of clinical trials. It maintains close relationships with regulatory bodies and ethics committees, and has a strong track record of successful projects and industry recognition.
Industries
Nr. of Employees
medium (51-250)
Products
Custom electronic patient follow-up and call-center system
Customer-oriented electronic tracking system and call-center solution for patient follow-up and pharmacovigilance activities.
eCRF / clinical database implementation
Design and implementation of electronic case report forms (eCRF) and clinical study databases, and support for eCRF-related audits.
Custom electronic patient follow-up and call-center system
Customer-oriented electronic tracking system and call-center solution for patient follow-up and pharmacovigilance activities.
eCRF / clinical database implementation
Design and implementation of electronic case report forms (eCRF) and clinical study databases, and support for eCRF-related audits.
Services
Regulatory consulting and preparation of submissions to ethics committees and regulatory authorities; protocol and CRF design support.
Clinical monitoring, CRA oversight and project management for trials across phases I–IV and post-marketing studies.
Study database construction, eCRF implementation and execution of statistical analyses according to the protocol.
Post-marketing surveillance and safety follow-up studies with dedicated safety management processes.
Training programs in clinical trials, GCP and study-specific procedures for site and sponsor personnel.
Support for translation of study documents and preparation of publications and scientific reports.
Regulatory consulting and preparation of submissions to ethics committees and regulatory authorities; protocol and CRF design support.
Clinical monitoring, CRA oversight and project management for trials across phases I–IV and post-marketing studies.
Study database construction, eCRF implementation and execution of statistical analyses according to the protocol.
Post-marketing surveillance and safety follow-up studies with dedicated safety management processes.
Training programs in clinical trials, GCP and study-specific procedures for site and sponsor personnel.
Support for translation of study documents and preparation of publications and scientific reports.
Expertise Areas
- Clinical trial management
- Regulatory affairs and submissions
- Data management and biostatistics
- Pharmacovigilance and safety management
Key Technologies
- Electronic data capture (eCRF)
- Clinical trial databases
- Biostatistics and statistical analysis
- Patient follow-up and call-center systems
News & Updates
Klinar CRO attended the online conference for the International Clinical Trials Day in May 2021.
Klinar CRO participated in the 2nd Kiev Clinical Research Forum, a global platform for the industry.
Klinar CRO participated in the EM-Phases conference focusing on best practices in multi-regional clinical trials.
Klinar CRO attended the workshop organized by İnönü University on clinical research excellence.
Klinar CRO participated in the symposium organized by Biotechnological Drugs Association in Ankara.
Klinar CRO attended the symposium on clinical research during COVID-19 in Istanbul.
Klinar CRO attended the online conference for the International Clinical Trials Day in May 2021.
Klinar CRO participated in the 2nd Kiev Clinical Research Forum, a global platform for the industry.
Klinar CRO participated in the EM-Phases conference focusing on best practices in multi-regional clinical trials.
Klinar CRO attended the workshop organized by İnönü University on clinical research excellence.
Klinar CRO participated in the symposium organized by Biotechnological Drugs Association in Ankara.
Klinar CRO attended the symposium on clinical research during COVID-19 in Istanbul.