Our Services
Study Initiation Services
Site Identification & Feasibility
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
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
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
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
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
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
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
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
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