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What is IXRS®3?

Our top-tier solution for overseeing patient randomization and trial supplies is offered in multiple formats, making it the most versatile and customizable Interactive Response Technology available today. Whether you're engaged in Phase I through Phase IV trials, and regardless of the complexity of your study design—be it simple or involving sophisticated adaptive methods—IXRS®3 is designed to accommodate any mix of study objectives. You will also have the advantage of a dedicated team of biostatisticians and integration specialists available 24/7 to assist you. The functionalities designed for site users enhance workflows that are usually prone to human error, enabling them to amend data independently without the need to reach out to a Help Desk or worry about compliance challenges. Instead of navigating through extensive pages filled with specifications and legal language, users can utilize intuitive visual tools that improve clarity. Moreover, you can keep track of and react to each phase of the software development process, which helps mitigate unforeseen issues during implementation, ensuring a more seamless trial experience. This holistic approach not only boosts operational efficiency but also grants users greater authority over their trial methodologies. Ultimately, this empowers research teams to conduct their trials with confidence and precision.

What is AcceleTrial?

AcceleTrial™ removes the guesswork involved in selecting and activating clinical trial sites. It operates on a Study Start-up Management System (SSMS) that prioritizes objective data over self-reported metrics, granting access to a vast repository of thousands of ranked sites around the world. These sites are assessed based on three crucial criteria: their relevant therapeutic knowledge, experience in conducting clinical trials, and available patient data. By utilizing this data-driven approach, you can effectively identify the best-fit sites globally for your clinical trials. The platform also supports a quick activation of these sites for patient enrollment through an automated "push and pull" system that is available in multiple languages. Moreover, it simplifies the document collection process with pre-filled templates and offers real-time activity tracking capabilities. Users can quickly adopt the system since it is cloud-based, requiring very little IT setup or training to get going. Additionally, AcceleTrial™ seamlessly integrates with CTMS or other clinical trial management software, which significantly boosts overall operational effectiveness. This groundbreaking method not only enhances the precision of site selection but also speeds up the entire process of study initiation, ensuring that trials can commence without unnecessary delays. Ultimately, AcceleTrial™ represents a significant advancement in the efficiency and reliability of clinical trial management.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
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

Almac Clinical Technologies

Company Location

United Kingdom

Company Website

www.almacgroup.com

Company Facts

Organization Name

LINEA System

Date Founded

2007

Company Location

United States

Company Website

www.lineasystem.com/acceletrial/

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

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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