Clinical Operations

At Turacoz, our Clinical Operations team is dedicated to ensuring the seamless execution of clinical studies, guiding you from initiation to successful completion. We provide comprehensive support throughout the clinical trial process, overseeing site selection, regulatory approvals, patient recruitment, study monitoring, and study close-out, while maintaining strict adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements.

Our Clinical Operations Expertise Includes

Study Planning and Feasibility

  • Define study objectives, endpoints, and population
  • Assess feasibility, data sources, and recruitment strategies

Regulatory and Ethics Compliance

  • Obtain institutional review board and ethics committee (IRB/EC) approvals (if required)
  • Ensure compliance with local regulations and data privacy laws

Site and Data Source Selection

  • Identify healthcare providers, registries, or electronic health records (EHR)
  • Establish partnerships with real-world data (RWD) sources

Patient Identification and Enrollment

  • Leverage EHR, claims data, or direct patient outreach
  • Obtain patient consent

Study Execution and Monitoring

  • Collect real-world data (RWD) through digital platforms, registries, or surveys
  • Monitor data quality, protocol adherence, and patient safety

Data Management and Analysis

  • Aggregate and clean real-world evidence (RWE)
  • Perform analytics to generate insights

Study Closeout and Reporting

  • Finalize database and conduct statistical analysis
  • Generate real-world study reports and insights

Regulatory and Market Access Support

  • Submit findings for regulatory or payer evaluation
  • Support publication and RWE generation for decision-making

Why Choose Turacoz?

  • Efficiency and Quality
    We focus on optimizing timelines and minimizing risks, ensuring that your clinical study progresses smoothly and efficiently, while delivering high-quality, reliable clinical data.
  • Compliant With Guidelines
    Our team is committed to maintaining strict adherence to GCP guidelines and all relevant regulatory requirements, ensuring that your trial remains compliant throughout its lifecycle.
  • Risk Mitigation
    By overseeing every aspect of the clinical study, we proactively identify and mitigate risks, ensuring the study is conducted without unnecessary delays or compliance issues.
  • Expertise You Can Trust
    With years of experience in clinical operations across a range of therapeutic areas, our team offers expert guidance and hands-on support to ensure the success of your clinical trials.

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