Our Services
Cliyana Research Solution is fully equipped to deliver a comprehensive spectrum of clinical research services, adhering strictly to GCP, GLP and all relevant regulatory and statutory standards. Our operations are rotted in uncompromising commitment to quality, data integrity, patient safety, and ethical excellence.
Our dedicated team comprises highly trained and experienced principal of investigator, clinical research coordinator, Nurses, Pharmacist and Phlebotomists, who form the core of our site management vertical. Each team member undergoes rigorous training in ICH-GCP, Indian regulatory frameworks and key international guidelines, ensuring that trial execution and documentation meet the highest standards of quality, integrity and compliance. Our comprehensive suite for services includes.
Project management
We deliver end to end project oversight to ensure clinical trials are initiated swiftly, executed flawlessly and completed on time. Our expert team drives site performance, accelerates patient recruitment and ensures full compliance with GCP and regulatory standards.
With a strong focus on timelines, regulatory compliance and patient-centric execution, our project managers act as the central link between sponsors, CROs, and trial sites ensuring clear communication, fast problem solving and optimal performance.
Site management
We are dedicated to simplifying and strengthening clinical trial execution at the site level. As a trusted Site Management Organisation, we partner with hospitals, clinics and patient-centric trial operations.
Our expert team manages the lifecycle of clinical research at the site from feasibility and startup to patient recruitment, regulatory support and data management.
Site Management Services includes
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Site Identification and feasibility
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Regulatory and Ethics Committee Support
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Patient Recruitment and Retention
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On-site Coordination and Monitoring
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Support
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Quality Assurance and GCP Compliance
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Training and Capacity Building for Site Staff.
Data Management
We understand that accurate, timely and compliant data is the foundation of successful clinical trials. Our data management team ensures high quality data capture and documentation at the site level, aligning with GCP, protocol requirements and sponsor expectations.
From source data verification to electronic data entry, we maintain complete data integrity throughout the trial lifecycle.
Early phase studies
We provide specialized site management services for early phase studies, including Bioavailability/Bioequivalence and Pharmacokinetics/Pharmacodynamics trials. Our trained teams and streamlined operations ensure high precision data collection, regulatory compliance and subject safety throughout the study lifecycle.