Clinical Trials

End-to-End CRO Solutions for Seamless Product Registration

Conducting local clinical trials is often essential for registering new medical products in Asian countries. Regulatory authorities across Asia may require localized clinical data, and the region’s genetically diverse population and cost-effective research infrastructure make it an ideal environment for clinical studies.

At Scansio, we offer comprehensive Clinical Research Organization (CRO) services tailored to meet regulatory expectations and deliver successful clinical trials for pharmaceutical, biotechnology, medical device, and IVD companies entering the Asian market.

Why Conduct Clinical Trials in Asia?

• Regulatory requirement for local data
• Access to large, diverse patient populations
• Cost-effective compared to Western countries
• Opportunity for post-market data generation and lifecycle management

Our Clinical Trial Services Include:

🧠 CRO and Clinical Strategy Consulting
Develop optimal trial strategies and protocols with insights from each target market’s regulatory landscape.

📄 Regulatory Support
Manage and submit Clinical Trial Applications (CTA) and Clinical Trial Notifications (CTN), and interface with local regulatory bodies and ethics committees (IRB/IEC).

📊 Clinical Trial Management
Oversee the entire trial process, including site selection, monitoring, data management, reporting, and gap analyses.

✅ Quality Compliance and Audits
Ensure trials align with GCP, GLP, GMP, GVP, GQP, and other quality standards through rigorous audits and compliance monitoring.

📈 Adverse Event Reporting & Post-Market Surveillance
Track and report adverse events during trials and assist with post-approval studies to maintain safety and efficacy over the product lifecycle.

With experienced, on-the-ground clinical teams and a deep understanding of Asia’s regulatory frameworks, Scansio ensures efficient and compliant clinical trials that accelerate your path to market entry.