Feyti limited is at the forefront of excellence in clinical trial design and management, offering unparalleled expertise and comprehensive solutions for organizations navigating the complex landscape of clinical research. With a commitment to advancing healthcare innovation, we specialize in guiding our clients through every stage of the clinical trial process, from meticulous protocol design to meticulous project management and regulatory compliance. Our distinguished services include; 

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Protocol Development: We specialize in crafting comprehensive plans that delineate the objectives, methodology, and statistical considerations crucial for a clinical trial. 

Adaptive Trial Design: We excel in implementing flexible trial designs that enable modifications based on interim data analysis. 

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Project Management: We assist in managing the complete lifecycle of the clinical trial, including overseeing timelines, budgets, and resource allocation. 

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Site Selection and Management: We aid in the identification and management of clinical trial sites, encompassing site initiation, training, and monitoring processes. 

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Data Management: we provide support in the collection, validation, and analysis of clinical trial data to ensure accuracy and compliance with regulatory standards. 

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Monitoring and evaluation: We conduct site visits to ensure protocol adherence, data accuracy, and compliance with Good Clinical Practice (GCP) guidelines. 

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Safety Monitoring: We assist in the implementation of safety measures and monitoring adverse events throughout the trial. 

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Audits and Inspections: We provide support in conducting both internal and external audits aimed at ensuring alignment with regulatory standards and compliance measures. 

Quality assurance: We help in establishing procedures aimed at monitoring and upholding the quality of activities associated with the trial. ​

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