KNOWLEDGE CENTRE
Data-Driven Patient Recruitment & Site Selection
Accelerate enrollment through Turkey’s high-volume clinical site network. We provide international sponsors with data-driven feasibility, seamless TİTCK compliance, and ICH-GCP standard strategies to ensure operational excellence and optimized global trial timelines.
Optimizing Global Clinical Timelines
Turkey offers global sponsors a significant competitive advantage: high-volume enrollment potential within an EU-aligned clinical trial framework. CROTURK bridges the operational gap by providing data-driven feasibility and site management strictly compliant with ICH-GCP and TİTCK standards. By prioritizing investigator experience and technical infrastructure, we establish a specialized foundation for success. Our localized approach ensures medical centers are activated with precision, delivering optimized timelines and high-quality data to meet your international trial objectives ahead of schedule.
Clinical Feasibility & Site Selection
Strategic site identification and recruitment planning are the primary drivers of clinical trial success. CROTURK bridges the clinical gap for international sponsors by leveraging Turkey’s high-volume therapeutic centers and EU-aligned regulatory framework to optimize enrollment timelines and data integrity.
DATA-DRIVEN FEASIBILITY
Strategic Site Identification
We qualify sites within 72 hours based on investigator experience, verified patient pool density, and technical infrastructure. This ensures 100% alignment with ICH-GCP standards and TİTCK regulatory requirements for rapid trial activation.
SITE SELECTION CRITERIA
Evidence-Based Site Mapping
Utilizing real-time performance metrics, we identify medical centers with proven histories of high recruitment and strict compliance. Our objective mapping minimizes screening failure rates and protects your recruitment budget.
RETENTION & ENGAGEMENT
Accelerated Enrollment Onset
We deploy proactive engagement strategies and specialized site staff training to minimize patient attrition. Our direct relationships with investigators ensure motivated site teams and consistent enrollment milestones ahead of schedule.
Strategic Recruitment & Site Excellence
Turkey provides clinical trial sponsors with a centralized, high-speed enrollment framework. At CROTURK, we leverage this infrastructure through data-driven feasibility and localized site management to protect your study budget and timelines, ensuring absolute adherence to ICH-GCP and TİTCK regulations.
Direct Patient Reservoir Access
Utilization of Turkey’s high patient density and treatment-naïve populations to mitigate recruitment bottlenecks in complex therapeutic areas.
Investigator-Centric Selection
Rigorous vetting of sites based on investigator experience, technical clinical infrastructure, and historically validated screening-to-randomization ratios.
TİTCK & Ethics Compliance
End-to-end management of regulatory submissions and ethical reviews, ensuring full clinical transparency and audit-ready documentation.
Retention & Operational Support
Proactive site monitoring, staff training, and specialized patient engagement strategies designed to minimize attrition and stabilize trial timelines.
Compliance & Ethical Integrity
Turkey offers international clinical sponsors a streamlined, EU-aligned framework. CROTURK provides end-to-end expertise in navigating the Turkish Medicines and Medical Devices Agency (TİTCK) requirements for expedited study activation and ethical oversight.
Regulatory Pathway Strategy
We coordinate cross-border regulatory submissions in full compliance with local directives. Direct liaison with Ministry officials eliminates bureaucratic delays, providing sponsors with predictable timelines for dossier approval and clinical site activation.
Ethics Committee Oversight
CROTURK manages both Central and Local Ethics Committee approvals, ensuring 100% adherence to submission cycles. Our recruitment plans prioritize ICH-GCP standards, maintaining participant safety and data integrity while optimizing enrollment speed.
THE CROTURK ADVANTAGE
Bridging Local Mastery with Global Excellence
Turkey represents a high-potential frontier for global pharmaceutical sponsors. At CROTURK, we bridge the clinical gap by combining deep localized TİTCK regulatory expertise with high-speed patient access via centralized medical hubs across the country.
Our data-driven feasibility strategies identify high-performing sites that consistently outperform Western recruitment benchmarks by 30-50%. We provide strategic monitoring and operational support, ensuring your trial milestones are achieved with absolute data integrity and ICH-GCP compliance.