As drug development accelerates and regulatory demands become increasingly complex, sponsors and CROs alike must take a more strategic, unified approach to clinical research. Integrated clinical trial services are no longer optional—they are essential for achieving global regulatory readiness, reducing time to market, and improving study quality across every phase. By bringing together site management, data collection, regulatory support, patient engagement, and monitoring into a single coordinated framework, integrated services eliminate inefficiencies, reduce handoff errors, and ensure that studies are conducted with a clear path toward international regulatory compliance. What Are Integrated Clinical Trial Services? Integrated clinical trial services refer to a comprehensive suite of solutions that support every stage…