Specialized Therapeutic Expertise

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

Pediatric & Neonatology Studies

Pediatricians in Türkiye are highly experienced in diagnosing and treating rare diseases in children. MonitorCRO has substantial experience in pediatric/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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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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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, leveraging relationships with approved investigator sites.

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Compassionate Use Programs

MonitorCRO partners with sponsors to obtain required Turkish Ministry of Health approvals for early patient access to medicines not yet available in the country.

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General Medicine & Bioequivalence

Broad therapeutic experience across interventional trials, observational studies, real-world evidence studies, and bioequivalence research for pharmaceutical and biotech sponsors.

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