ShareCRF Reviews & Ratings

ShareCRF

4.7 out of 5 stars

Ratings and Reviews 0 Ratings

Total 0 out of 5 stars
ease 0 out of 5 stars
features 0 out of 5 stars
design 0 out of 5 stars
support 0 out of 5 stars

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Ratings and Reviews 7 Ratings

Total 4.5 out of 5 stars
ease 4.5 out of 5 stars
features 4.5 out of 5 stars
design 4.5 out of 5 stars
support 5 out of 5 stars

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What is TrialStat?

In comparison to other Electronic Data Capture (EDC) systems offered by firms like MediData, DataTrack, and Omnicomm, TrialStat emerges as the most all-encompassing suite of tools for study management, providing seamless integration with a variety of external data sources such as electronic medical records (EMR), wearable technology, and both clinical and non-clinical information systems. TrialStat offers a unified platform that supports every stage and type of clinical trial. Our EDC suite is equipped with a single sign-on feature and accommodates multiple tenants, featuring modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, a Vendor Neutral Imaging Archive, a comprehensive Reporting and Analytics Portal, and customized Machine Learning solutions. With a strong focus on data analysis, TrialStat ensures real-time reporting, on-demand data extracts, and analytics that encompass a single study, a program, or the full breadth of your research portfolio, providing all stakeholders with relevant, tailored, and timely insights into all aspects of study data while identifying potential risks or delays. Furthermore, the platform’s robust integration capabilities enhance collaboration among research teams, resulting in a more streamlined and productive trial management process. This ultimately empowers researchers to make informed decisions that drive the success of their clinical trials.

What is ShareCRF?

Within just a few hours, you can design an electronic Case Report Form (eCRF) that is as user-friendly and straightforward as its paper counterpart. This approach will significantly reduce the typical challenges encountered in data collection for both pre-authorisation and post-authorisation studies. When you set out to create an eCRF, it’s crucial to utilize an Electronic Data Capture (EDC) system that offers flexibility, enabling you to customize it for various study types. Additionally, the EDC comes equipped with several monitoring and management tools that can greatly streamline the study oversight process, saving you both time and energy. It is essential to employ a reliable system that instills confidence in the sponsor and facilitates the gathering of high-quality data. Addressing any data errors only during the analysis phase can lead to complications, as it may require you to track down investigators for corrections after the fact. Therefore, strive to keep the eCRF creation process efficient and straightforward, ensuring that it meets all necessary requirements without unnecessary complexity. By focusing on these elements, you can enhance the overall effectiveness and accuracy of your research.

Media

Media

Integrations Supported

Integrations Supported

IBM SPSS Statistics
Microsoft Excel
SAS Analytics Pro

API Availability

API Availability

Has API

Pricing Information

Pricing not provided

Pricing Information

$500/month
Price only based on number of participants and required add-ons. There is no limit to the number of sites or users.
Free Trial Offered?

Supported Platforms

SaaS

Supported Platforms

SaaS

Customer Service / Support

Web-Based Support

Customer Service / Support

Standard Support
Web-Based Support

Training Options

Documentation Hub

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

TrialStat Solutions

Company Location

United States

Company Website

trialstat.com

Company Facts

Organization Name

ShareCRF

Company Website

www.sharecrf.com

Categories and Features

Categories and Features

Clinical Trial Management

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

Electronic Data Capture

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Forms Management
Remote Capture
Study Management

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