Our Services

Comprehensive Clinical Research Solutions – From Study Design to Data Submission

Clinical Trial Execution

Fast-Track Regulatory Approvals – With one of the fastest approval timelines in the world (as little as 2 months) and a WHO Level 3–recognized regulatory agency, we ensure a seamless, globally compliant approval process for rapid study initiation.
Optimized Patient Recruitment – Leveraging a 150,000+ patient database and strong partnerships with a large private hospital and the leading Cancer Research Center, we cut enrollment time by 50% compared to traditional markets.
Phase I-III Expertise – Our experienced clinical team has 15+ years of experience managing clinical trials conducted, with participants cohorts ranging from 9 to 2,000 participants while maintaining 100% patient retention record.
Integrated Site & Trial Management – We provide comprehensive site management services, ensuring efficient trial operations, compliance with ICH-GCP standards, and seamless coordination between investigators, sponsors, and regulatory agencies.

Compliance with Standards: Our team has a strong record in navigating the regulatory landscapes of the U.S. and Europe, ensuring that all trial activities adhere to the highest standards, thereby expediting approval processes (ICH-GCP, FDA & EMA Compliance)
Data Integrity & Quality Assurance: We adhere to FDA 21 CFR Part 11-compliant electronic data capture systems, ensuring full transparency and auditability.