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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.

What is Astracore Clinical Trials?

Our platform for managing clinical trials is engineered to support virtually any form of controlled clinical trial, including randomized studies, and provides a range of randomization algorithms. This versatile software can be easily configured for both paper Clinical Report Forms (CRFs) and electronic CRFs (eCRFs). It is adept at capturing data in various formats and methods, adhering to the specific guidelines you set to maintain data integrity and quality assurance. The system allows for direct Electronic Data Capture (EDC) via eCRFs, or it can generate paper CRFs that can subsequently be entered into the system. Additionally, users can upload a variety of media including images, audio recordings, videos, and documents such as consent forms, with the only constraint being the available storage space. The platform incorporates Double Data Entry and offers thorough exception reporting to ensure accuracy. Furthermore, it features a mechanism to lock records once they have been validated, preventing any further modifications. This extensive functionality significantly bolsters the reliability of the data gathered throughout the trial, thus enhancing the overall research quality. Overall, our platform is designed to streamline the clinical trial process while ensuring the highest standards of data management and security.

Media

Media

Integrations Supported

IBM SPSS Statistics
Microsoft Excel
SAS Analytics Pro

Integrations Supported

IBM SPSS Statistics
Microsoft Excel
SAS Analytics Pro

API Availability

Has API

API Availability

Has API

Pricing Information

$500/month
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

ShareCRF

Company Website

www.sharecrf.com

Company Facts

Organization Name

Astracore

Date Founded

2010

Company Location

Australia

Company Website

astracore.com/medical/clinical/

Categories and Features

Clinical Trial Management

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

Electronic Data Capture

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

Categories and Features

Clinical Trial Management

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

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