Modern Clinical Trial Management System | Yuva Infocare

1. Clinical Trial Management System - Yuva Infocare What Is a CTMS? A Clinical Trial Management System (CTMS) is a specialized software solution designed to manage, track, and organize the entire operational lifecycle of clinical trials. It helps study teams streamline planning, site setup, subject tracking, monitoring, compliance, finances, and reporting — all in one place. In today’s complex research environment, a modern CTMS is essential to: Improve operational efficiency Minimize errors and delays Ensure protocol and regulatory compliance Provide real-time visibility into trial progress Support faster, data-driven decision-making Clinical Trial Management in the Modern Era The life sciences industry is undergoing a rapid digital transformation. As clinical trials become more complex, globally distributed, and highly regulated, traditional manual processes are no longer sufficient. Today, sponsors, CROs, and research teams require smarter, integrated, and compliant solutions to manage the full lifecycle of clinical trials. This shift is why Modern CTMS Is the Future of Pharma— enabling organizations to streamline operations, reduce delays, improve collaboration, and maintain regulatory integrity across every study phase.

2. Introducing ARS CTMS by Yuva Infocare Yuva Infocare’s ARS CTMS is a modern, cloud-based Clinical Trial Management System built for pharmaceutical, biotech, and CRO organizations. It enables teams to manage studies with precision, automation, and complete regulatory compliance. What makes ARS CTMS unique? Part of the ARS Unified Clinical Suite Fully cloud-native, scalable, and secure Compliant with 21 CFR Part 11, ICH-GCP, and GxP Real-time dashboards and KPI-driven trial oversight Seamless integration with ARS EDC, ARS IWRS, ARS eTMF, ARS PV, ARS ePRO, and ARS EDX Comprehensive audit trail and advanced security features Key Features of ARS CTMS Study & Protocol Management Plan and organize study timelines, milestones, and protocol-driven tasks. Site Management

3. Simplify site selection, activation, monitoring, communications, and closeout processes. Subject Tracking Track enrollment, visits, deviations, drop-outs, and performance across all sites. Monitoring & CRA Oversight Schedule monitoring visits, manage CRA tasks, and generate monitoring reports. Budgeting & Financial Management Automate site payments, track costs, and manage investigator grants. Dashboards & Analytics Real-time study metrics, site performance, and operational insights. Regulatory & Compliance Tools Electronic signatures, audit trails, version control, and role-based access. Integration Capabilities Connect effortlessly with ARS Suite modules and external clinical systems. Benefits of ARS CTMS Higher Efficiency Real-Time Oversight Reduced Risk Better Cost Control Improved Decision-Making Flexible & Scalable Suitable for small biotech to global large-scale trials.