What is Clinevo CTMS?

Clinevo's Clinical Trial Management System (CTMS) offers a robust, cloud-based solution tailored to effectively manage all aspects of clinical trials with a high degree of customization. The platform complies with essential regulatory requirements, incorporating security features, access controls, change management strategies, audit trails, and validation processes to ensure maximum compliance and dependability. This comprehensive approach not only streamlines trial management but also enhances the overall integrity of clinical research.

Integrations

No integrations listed.
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Screenshots and Video

Clinevo CTMS Screenshot 1
Clinevo CTMS Screenshot 1 Clinevo CTMS Screenshot 2

Company Facts

Company Name:
Clinevo Technologies
Company Website:
www.clinevotech.com

Product Details

Deployment
SaaS

Product Details

Target Company Sizes
Individual
1-10
11-50
51-200
201-500
501-1000
1001-5000
5001-10000
10001+
Target Organization Types
Mid Size Business
Small Business
Enterprise
Freelance
Nonprofit
Government
Startup
Supported Languages
English

Clinevo CTMS Categories and Features

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 Customer Reviews

Write a Review
  • Reviewer Name: Manoj K.
    Position: Head -CT and PV
    Has used product for: Less than 6 months
    Uses the product: Daily
    Org Size (# of Employees): 1 - 25
    Feature Set
    Layout
    Ease Of Use
    Cost
    Customer Service
    Would you 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
    • This system provides the user with any information they want for study/project on real time basis.
    • 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.
    • The System offers a secure, centralized location for data collection, storage and retrieval.
    • It keeps track of a study's financial data, ensuring accurate invoicing for sponsors and proper payments for each site.
    • 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.
    • Major and Minor protocol deviation can be tracked at study and site level.
    • 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.

    Read More...
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