Our Services
Study Initiation Services
Site Identification & Feasibility
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We help sponsors identify high-performing and protocol-appropriate clinical trial sites through thorough feasibility assessments based on investigator expertise, patient availability, past performance, and infrastructure readiness
Site onboarding and Training
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​We streamline the onboarding of new sites by aligning investigators, coordinators, and support staff with the study protocol, SOPs, and sponsor expectations through customized training modules.
Regulatory & Ethics Submissions
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Our team manages end-to-end regulatory and IEC/IRB submissions - including preparation, tracking, and follow-up to ensure timely approvals and compliance with ICH-GCP and local regulatory requirements.
Trial Execution Services
Patient Recruitment & Retention
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We deploy targeted outreach strategies, local partnerships, and patient engagement tools to drive recruitment while ensuring participant satisfaction and retention throughout the study duration.
Site monitoring and coordination
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​Our dedicated clinical coordinators ensure that all trial activities are executed per protocol by supporting daily site operations, maintaining communication with sponsors/ CROs, and managing visit logistics
Data Collection & Documentation
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We ensure accurate and timely data capture across source documents, CRFs/eCRFs, and essential logs while supporting sites in maintaining documentation that is inspection- and audit-ready.
Training and Certification
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We offer protocol-specific training, GCP refreshers, and role-based certifications for investigators and site staff to maintain quality and compliance standards across all trial phases.
Quality & Close-Out Services
Audit Readiness
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We deploy targeted outreach strategies, local partnerships, and patient engagement tools to drive recruitment while ensuring participant satisfaction and retention throughout the study duration.
Site Close-Out & Archival
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​Our dedicated clinical coordinators ensure that all trial activities are executed per protocol by supporting daily site operations, maintaining communication with sponsors/ CROs, and managing visit logistics