Clinevo Clinical Trial Management System (CTMS)

Clinevo Clinical Trial Management System (CTMS) is a cloud based, highly configurable, "end-to-end platform which" helps manage all aspects of clinical trials including :

• Site Monitoring Visits
• Milestones - Planning and Tracking
• Activities - Tasks  & Deviations
• Payments - Site & Investigator
• Investigational Product (IP) Tracking &  Inventory (IWRS)
• Patient Recruitment & Randomization (IWRS)
• Patient Visits - Scheduling and Tracking
• Site Selection, Site Initiation, Investigator Selection
• Master Data Management (Sites, Investigators)
• Regulatory documents & Compliance Tracking
• Study Budgets & Training Management
• Adverse Event Tracking and many more.

Clinevo Clinical Trial Management System (CTMS) meets the regulatory guidelines including security, access control, change controls, audit trails, and the best system validation.

A Clinical Trial Management System (CTMS) is a software application that supports the Clinical trial processes. It provides infrastructure, consisting of three components: Clinical Data Management System (CDMS), Site Management System (SMS), and a Patient Recruitment Database or a Clinical Trial Web Portal that enable a site to plan, implement, monitor, analyze and report on clinical research activities to maximize the probability of delivering high-quality data within time and budget constraints.