Clinical Trial Management System (CTMS) for Clinical trials Software in Bangalore, India, USA & Europe
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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 system validation.

Image

Image One Clinical Trial System

  • An end-to-end Clinical Trial Management System (CTMS) system with integration to eTMF and Training Management Systems

Image​ Compliance Alerts

  • Clinevo Clinical Trial Management System (CTMS) provides end user alerts for regulatory documents, milestones, site and subject visits, tasks / action items, trainings of the clinical trials

Image Dynamic workflows

  • Clinevo Clinical Trial Management System (CTMS) provides easily configurable workflows to meet the Sponsor SOPs and every requirement of clinical trials

Image Integrated Master Data Management

  • Clinevo Clinical Trial Management System (CTMS) ships with an inbuilt Master Data Management module to manage Sites, Investigators, Products and other master data in a centralized repository provides a higher level of reusability of the information in different clinical trials.

Image Feature-rich and flexible

  • Clinevo Clinical Trial Management System (CTMS) consists of documents, activities, contacts, schedules, payments, milestones and more.

Image Regulatory Inspection Ready

  • Clinevo Clinical Trial Management System (CTMS) complies with all current and emerging regulations including 21 CFR Part 11, ANNEX 11, GxP, and GDPR.

Image Real time monitoring and reporting

  • Clinevo Clinical Trial Management System (CTMS) provides powerful and actionable dashboards and reports for real time monitoring and tracking of study and site statuses

Image Cost Effective & High Performing

  • Clinevo Clinical Trial Management System (CTMS) is a cost-effective system comes with transparent optimized pricing.
  • Clinevo Clinical Trial Management System (CTMS) is built on a committed infrastructure, hosting, training, business process and 24/7 application support.

Image Faster User Adoption

  • Business team, CROs, and others can be trained on the Clinevo Clinical Trial Management System (CTMS) within few hours.

Image Anytime, Anywhere & Any device

  • Clinevo Clinical Trial Management System (CTMS) is user-friendly web application which can be accessed with internet / intranet using IE, Chrome and Firefox browsers

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Call us now:
USA : +1 – 315 232 8028
 INDIA : +91- 44 6645 5983

Reach us Now:
info@clinevotech.com

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