Clinical Trial Management
Welcome to phairen's comprehensive solutions in Clinical Data Management, Biostatistics, Statistical Programming, and Medical Writing. Our team is committed to delivering high-quality services tailored to meet your specific needs, ensuring that your research and data management requirements are successfully met. We also specialize in CDISC standards to ensure regulatory compliance and data integrity.
Clinical Trial Management
1
Study Design & Protocol Development
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Design scientifically sound clinical trial protocols based on study objectives
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Develop statistical analysis plan and define study endpoints
2
Site Selection & Feasibility
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Assess clinical research center resources
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Evaluate investigator capabilities and patient recruitment potential
3
Project Management
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Comprehensive trial progress management
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Risk control and quality assurance
4
Trial Monitoring
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Regular CRA (Clinical Research Associate) monitoring visits
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Ensure compliance with GCP (Good Clinical Practice)