Specialized Therapeutic Expertise

Deep domain knowledge across high-impact areas of focus, backed by 25+ years of clinical research experience in Türkiye.

Early Phase Trials

MonitorCRO pioneered the first Phase I clinical study in Türkiye in 2004 and has contributed substantially to Phase I trial setup across the country. We have enabled the opening of many Phase I centers in Türkiye and are among the most active organizations conducting early phase research nationwide.

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Phase II to IV Studies

MonitorCRO provides full-service management of Phase II, III, and IV clinical trials across a broad range of therapeutic areas, from study start-up through monitoring to close-out and reporting.

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Medical Device Studies

MonitorCRO understands medical device and diagnostics regulations. From regulatory applications to study execution and product approvals, including MDR post-market surveillance via Helios EDC.

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Pediatric & Neonatology Studies

Pediatricians in Türkiye are highly experienced in diagnosing and treating rare diseases in children. MonitorCRO has substantial experience in pediatric and neonatology studies, navigating complex regulatory pathways for efficient, successful trials.

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Orphan Drugs & Rare Diseases

Türkiye has unique demographics with higher incidences of rare hereditary diseases. MonitorCRO has excellent experience with orphan drug applications and follow-up inspections with the Ministry of Health.

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PK Studies & Bioequivalence

MonitorCRO has broad experience managing pharmacokinetic and bioequivalence studies for pharmaceutical and biotech sponsors, supporting generic, biosimilar, and new product development.

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Therapeutic Areas We Cover

Across these areas of focus, we have delivered studies in a wide range of therapeutic fields, including:

Oncology & Hematology

Cardiology

Neurology & CNS

Endocrinology & Metabolism

Immunology & Rheumatology

Infectious Diseases

Gastroenterology

Respiratory

Dermatology

Nephrology

Ophthalmology

Vaccines