Clinevo CTMS Description

Clinevo's Clinical Trial Management System (CTMS) is a comprehensive, cloud-based platform designed to efficiently oversee every facet of clinical trials while being highly customizable. It adheres to all necessary regulatory standards, encompassing security measures, access management, change control protocols, audit trails, and system validation processes for optimal compliance and reliability.

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Integrations

No Integrations at this time

Reviews - 1 Verified Review

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Company Details

Company:
Clinevo Technologies
Website:
www.clinevotech.com

Media

Clinevo CTMS Screenshot 1
Clinevo CTMS Screenshot 1 Clinevo CTMS Screenshot 2
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Product Details

Platforms
Web-Based

Clinevo CTMS Features and Options

Clinical Trial Management Software

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Clinevo CTMS User Reviews

Write a Review
  • Name: Manoj K.
    Job Title: Head -CT and PV
    Length of product use: Less than 6 months
    Used How Often?: Daily
    Role: Administrator
    Organization Size: 1 - 25
    Features
    Design
    Ease
    Pricing
    Support
    Likelihood to Recommend to Others
    1 2 3 4 5 6 7 8 9 10

    Excellent CTMS Covering all Study Related Activities

    Date: Mar 05 2021

    Summary: It is really great experience while implementing the CTMS and also other tools from Clinevo like eTMF, EDC, QMS, TMS and PV database.

    Positive: Excellent CTMS Covering all Study Related Activities
    β€’ This system provides the user with any information they want for study/project on real time basis.
    β€’ The main goal of our CTMS to create a global system to streamline the clinical trial process, enhance the productivity, Improve client and site relationship.
    β€’ The System offers a secure, centralized location for data collection, storage and retrieval.
    β€’ It keeps track of a study's financial data, ensuring accurate invoicing for sponsors and proper payments for each site.
    β€’ Many research sites and institutions conduct hundreds of clinical trials every year, and a CTMS can help improve the overall efficiency within each trial.

    Negative: eLog was not available but it is already in implementation stage now.
    It provides functionality for tracking and managing regulatory information across the enterprise, such as amendments, protocol and subject deviations, and more. Additionally, staff credentials can also be tracked within the system.
    β€’ Major and Minor protocol deviation can be tracked at study and site level.
    β€’ CTMS is connected with eTMF and EDC so the activities which are done in CTMS can be directly captured in the respective section of eTMF and EDC system.

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