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Clinical Conductor CTMS is an industry-leading clinical trial management system (CTMS) trusted by health systems, hospitals, site networks, and dedicated research sites. It streamlines operational, financial, and regulatory workflows to improve efficiency and quality across the research lifecycle. Backed by Advarra's expert team with deep experience in research operations, Clinical Conductor offers true enterprise capabilities that enable organizations to scale—supporting growth, high study volumes, and multi-site management. The platform delivers comprehensive, end-to-end functionality, including strong financial management workflow management, protocol management, participant recruitment, visit tracking, scheduling, and financial reporting. Clinical Conductor also features exclusive, turnkey integrations with Advarra’s eReg and eSource systems, enhancing connectivity and driving greater efficiency across research workflows.
RealTime-CTMS is a clinical trial management system designed to streamline operations within a clinical research site.
Trialytix is the first software that covers all essential budget and cost operations of your clinical trial project.
UpSite Clinical offers TrialPro, an AI-enabled clinical trial budgeting software designed to assist research sites, sponsors and CROs in creating and negotiating study budgets and Medicare coverage analysis. The tool uses Fair Market Value benchmarks and automates various budgeting processes to ensure that sites avoid unpaid work and save time. Built by industry veterans, TrialPro analyzes protocols and generates budget grids while identifying unbudgeted work and generating coverage analysis. Their services cater to clinical research sites, sponsors and CROs seeking efficient and effective budget management solutions.
With a real-time view across clinical trial processes, Vault CTMS improves operational efficiency, streamlines collaboration, and enables faster, higher-quality trial execution.
Medidata is committed to optimizing clinical trials from concept to conclusion—beginning with protocol design, through execution and management of the clinical trial, to conclusion with actionable data for effective decision making.