Ennov CTMS 2026: Benefits, Features & Pricing

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Overview
Pricing and Plans
Features
Integrations
User Reviews

Overview

Ennov CTMS

2.0

(2)

Pricing

Starting at €5,000.00 per year

About Ennov CTMS

Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, make better decisions, ensure compliance, select investigators well, manage finances, monitor patient recruitment. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers).

This platform offers functions for tracking patients, patient visits, EDC data, queries, adverse events, deviations, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible.

Ennov CTMS Screenshots

Ennov CTMS Pricing and Plans

Starting price: €5,000.00 per year

Free Trial

Free Version

Basic

€5,000.00

per user, per year

No plan information available

Ennov CTMS Features

Popular features found in Clinical Trial Management
21 CFR Part 11 Compliance
Data Capture and Transfer
Data Import/Export
Document Management
Electronic Data Capture
Financial Management
Inventory Management
Patient Management
Patient Monitoring
Patient Recruiting
Scheduling
Workflow Management
More features of Ennov CTMS
Access Controls/Permissions
Activity Dashboard
Activity Tracking
Ad hoc Reporting
Alerts/Notifications
API
Audit Management
Audit Trail
Calendar Management
Clinical Study Management
Compliance Management
CRF Tracking
Customizable Forms
Customizable Reports
Data Synchronization
Data Verification
Data Visualization
Digital Signature
Document Storage
Double Data Entry
Drag & Drop
EMR/EHR
Forms Management
HIPAA Compliant
Monitoring
Progress Tracking
Randomization
Real-Time Data
Real-Time Monitoring
Real-Time Reporting
Reminders
Reporting & Statistics
Role-Based Permissions
Third-Party Integrations
User Management

Ennov CTMS Integrations

Google Drive

Microsoft 365

OneDrive

Google Docs

Ennov CTMS User Reviews

Overall Rating

2.0

Ratings Breakdown

50%

Secondary Ratings

Ease of Use

2.0

Value for money

2.0

Customer support

1.0

Functionality

1.5

Have you used Ennov CTMS and would like to share your experience with others?

Verified

Reviewer

Research

1001-5000 employees

Used daily for more than 2 years

Review source

Reviewed November 2018

outdated software?

Ennov CTMS helped academic research to develop its own data management activities in the early 2000s. Today, the user interface is obsolete and the software performance does not allow to handle large volumes of data effectively (EDC, cleaning and export)

Ratings Breakdown

Ease of use

Value for money

Customer support

Functionality

Pros:

A CTMS by a french companyie Ease of use on small studies

Cons:

Real lack of performance and efficiency on high data volumes and complex clinical studies

Harry P.

Verified reviewer

Research

2-10 employees

Used monthly for less than 2 years

Review source

Reviewed September 2021

Mit Abstand schlechtester CRF, mit dem ich je gearbeitet habe

Benutzerunfreundlich, unübersichtlich, langsam, Features unverständlich

Ratings Breakdown

Ease of use

Functionality

Pros:

Leider hat mir an dieser Software nichts gefallen. Dies hat sich auch nach mehrfachen Updates nicht geändert.

Cons:

Ich arbeite seit fast 30 Jahren in der klinischen Forschung, davon seit gut 20 Jahren mit elektronischen Datenerfassungssystemen (Electronic Data Capture, Electronic Case Report Forms). Der Ennov Clinical, mit dem ich leider in einer großen, sehr komplexen Studie in der Intensivmedizin arbeiten muss, ist ohne Übertreibung der mit Abstand schlechteste eCRF, mit dem ich je gearbeitet habe. Es ist eigentlich unverantwortlich, wieviel Extrazeit benötigt wird, zum einen von Seiten des klinischen Zentrums, das die Dateneingabe machen muss und zum anderen von meiner Seite, der ich diese Daten überprüfen muss. Bei sehr vielen Features hat man den Eindruck, dass die Entwickler nicht wissen, was ein CRF in einer klinischen Studie leisten muss.

Showing 1 - 2 of 2 Reviews