BREEZE CTMS Description

Electronic source documents - eSource – eliminate paper, standardize and simplify workflow and reduce errors and omissions. BREEZE eSource does more than just schedule visits and create templates. BREEZE eSource synchronizes clinical contexts, regulatory requirements, and protocol requirements with study procedures. This ensures that users capture all protocol-required data. BREEZE business rules ensure that data collected is accurate, complete, accurate, and in compliance with regulations. Our dedicated team of clinical trial specialists delivers customized, study-specific eSource documents to review and approve before study start-up. They also support you throughout the trial by modifying them as necessary. Modules work seamlessly together. Cross-Module Action Multiplier takes things one step further, anticipating and completing automatically any additional tasks you enter. For example, the completion of visits or procedures automatically posts invoicing, recalculates scheduling, etc.

Integrations

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Reviews - 1 Verified Review

Total
ease
features
design
support
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Company Details

Company:
BREEZE CTMS
Headquarters:
United States
Website:
www.breezectms.com

Media

BREEZE CTMS Screenshot 1
BREEZE CTMS Screenshot 1
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Product Details

Platforms
SaaS
Customer Support
Phone Support

BREEZE 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

BREEZE CTMS User Reviews

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  • Name: Anonymous (Verified)
    Job Title: Director
    Length of product use: 2+ Years
    Used How Often?: Daily
    Role: User, 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

    Superior clinical trials app!

    Date: Jan 24 2022

    Summary: Truly a game changer for us. Reduced staff needs by 75% and increased study capacity and revenues arithmetically.

    Positive: Automates user workflows. PI oversight. Enforces protocol and GCP compliance seamlessly. VERY user friendly. Integrates eSource, eRegulatory, eConsent with financials so it captures everything with no redundant data entry. Staff, monitors, and FDA inspectors love it.
    Got its name from a monitor saying, "It's a breeze!"
    All at affordable pricing and dynamite support.

    Negative: There is not much not to like with BREEZE. The support and trial configurations are easy to work with. Deviations are reduced. We can document and report SAE's and Deviations in under 5 minutes, and we no longer miss protocol required data or GCP steps.

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