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) and regulatory requirements.

Our Clinical Operations Expertise Includes:

Study Planning & Feasibility

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

Regulatory & Ethics Compliance

  • Obtain IRB/EC approvals (if required)
  • Ensure compliance with local regulations and data privacy laws

Site & Data Source Selection

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

Patient Identification & Enrolment

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

Study Execution & Monitoring

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

Data Management & Analysis

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

Study Closeout & Reporting

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

Regulatory & Market Access Support

  • Submit findings for regulatory or payer evaluation
  • Support publication and real-world evidence generation for decision-making

Why Partner with Us?

  • Efficiency & Quality
    We focus on optimizing timelines and minimizing risks, ensuring that your clinical study progresses smoothly and efficiently, delivering high-quality, reliable clinical data.
  • Compliant with GCP & Regulatory Standards
    Our team is committed to maintaining strict adherence to Good Clinical Practice (GCP) 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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