Comprehensive SMO Services for Clinical Trials
Site Identification & Feasibility Assessment
Clinical Trial Site Setup & Management
Ethics Committee Creation & Management Support
Ethics Committee Documentation & Submission Coordination
ICH-GCP & Regulatory Compliance Management
Regulatory Document Preparation & Maintenance
Trained PI, Co-I & Clinical Research Coordinator Support
Investigator & Site Staff Training Programs
Patient Recruitment & Retention Support
Source Documentation & Clinical Data Management
Study Startup, Conduct & Close-Out Support
Monitoring, Quality Assurance & Audit Readiness
Pharmacovigilance & Safety Reporting Support
Laboratory, Diagnostic & Sample Management Coordination
Digital Clinical Trial Operations & Tracking
Sponsor, CRO & Site Communication Management
Multi-Center & Pan-India Trial Coordination
Infrastructure & Hospital Research Site Development
Subject Visit Coordination & Follow-Up Management
End-to-End Clinical Trial Operational Support
1. For Existing Clinical Trial Sites
We collaborate with hospitals and research sites that are already conducting clinical trials and are looking to expand their clinical research capabilities across multiple therapeutic areas. Our team provides complete operational, regulatory, and site management support to strengthen study execution, patient recruitment, quality systems, and sponsor readiness. We help sites enhance their research infrastructure with advanced digital processes, trained research staff, and strong ICH-GCP compliance standards to achieve long-term clinical research growth and excellence.
2. For New Sites Interested in Clinical Research
We support hospitals and healthcare centers that are planning to start clinical trial activities and establish a dedicated Clinical Research Department. Our SMO provides complete guidance for setting up research infrastructure including Ethics Committee (EC) registration and management, regulatory documentation, SOP development, staff training, ICH-GCP compliance, digital trial management systems, and investigator support. We aim to build high-quality, audit-ready, and sponsor-friendly clinical research departments with the best operational and compliance standards for successful clinical trial conduct.