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Average Ratings 0 Ratings

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ease
features
design
support

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Write a Review

Description

Electronic source documents, known as eSource, replace traditional paper methods, streamline workflows, and minimize the likelihood of errors and omissions. BREEZE eSource transcends basic visit templates and scheduling functionalities. By aligning clinical contexts with regulatory and protocol requirements, along with study procedures, BREEZE eSource ensures users effectively capture all necessary data mandated by the protocol. The business rules within BREEZE guarantee that data collected are not only correct but also complete, precise, and compliant with relevant standards. Our team of clinical trial specialists creates tailored eSource documents specific to each study for review and approval prior to the trial's initiation, providing ongoing support and adjustments throughout the study duration. The individual modules integrate flawlessly, working in unison to enhance efficiency. The Cross-Module Action Multiplier further elevates functionality by predicting and automatically fulfilling supplementary tasks based on user inputs, such as automatically recording completed visits or procedures, which then updates invoicing and recalibrates scheduling effortlessly. This interconnected approach not only simplifies trial management but also enhances overall data integrity and operational effectiveness.

Description

The platform features a sleek and user-friendly design, ensuring that navigation and data entry are both swift and effortless; it incorporates access control measures and SSL encryption for security, operates entirely online without the need for installations, and includes built-in monitoring alongside tools for data management and reporting, with a monthly flat rate (SaaS) that is customizable based on the size and duration of the study. Data collection is accelerated through an accessible web interface, allowing users to easily review the status of data completion with visual indicators, while it also employs edit checks and both automatic and manual queries to identify any discrepancies; additionally, it offers source data verification (SDV) and remote reviews through integrated buttons, meticulously tracking all changes made, including the author, date, time, and reason for each modification, and it can generate datasets (e.g., CSV) for subsequent statistical analysis, providing a comprehensive solution for research needs. This robust functionality ensures that users can efficiently manage their data while maintaining high standards of accuracy and security throughout the research process.

API Access

Has API No 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

Lybra Assistant Yes 
iPublish Media Yes 

Integrations

Lybra Assistant No 
iPublish Media No 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support No 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support Yes 

Types of Training

Training Docs No 
Webinars No 
Live Training (Online) No 
In Person No 

Types of Training

Training Docs Yes 
Webinars No 
Live Training (Online) Yes 
In Person No 

Vendor Details

Company Name

BREEZE CTMS

Country

United States

Website

www.breezectms.com

Vendor Details

Company Name

Sofpromed

Founded

2012

Country

Spain

Website

www.sofpromed.com

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance Yes 
Document Management Yes 
Electronic Data Capture Yes 
Enrollment Management No 
HIPAA Compliant No 
Monitoring No 
Patient Database No 
Recruiting Management No 
Scheduling Yes 
Study Planning No 

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance Yes 
Document Management Yes 
Electronic Data Capture Yes 
Enrollment Management Yes 
HIPAA Compliant Yes 
Monitoring Yes 
Patient Database Yes 
Recruiting Management Yes 
Scheduling No 
Study Planning No 

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