At JCPR, quality is the foundation of every study we conduct. We maintain a comprehensive and rigorously implemented Quality Management System built on carefully developed Standard Operating Procedures (SOPs) that address every aspect of our operations—clinical conduct, bioanalysis, safety, documentation, data integrity, storage, and reporting. Each process is designed to meet and exceed ICH-GCP, GLP, EMA, JFDA, and other international regulatory requirements.

Our team undergoes continuous specialized training covering equipment operation, analytical procedures, documentation standards, and report generation to ensure consistent, reproducible, and reliable results.

For nearly three decades, JCPR has invested heavily in strengthening its quality systems, prioritizing the well-being of our staff and volunteers while maintaining seamless study execution that aligns with national and international guidelines. As one of the few fully independent CROs in the region, we operate without external shareholders or investor pressure. This independence enables complete transparency, integrity, and ethical conduct, and allows us to reinvest the majority of our resources into operations, quality assurance, bioanalysis upgrades, and senior oversight.

At JCPR, quality is not just a requirement—it is a long-standing commitment embedded in every phase of our work.