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What is Trials.ai?

Our cutting-edge Smart Protocol system is engineered to integrate automation and advanced intelligence into the architecture of clinical trials through the use of artificial intelligence. This revolutionary system is reshaping the outdated manual methods that research teams have depended upon for designing clinical trials. In the current digital era, it has become nearly impossible for individuals to meticulously examine every aspect necessary for making informed decisions. Additionally, a multitude of organizations hold precious data that often remains underutilized, with documents stored in systems that lack adequate access. As a result, life science companies may end up making substantial and costly decisions based on inadequate information. Our mission is to shift organizations like yours from a focus on document-centric practices to a more insightful, data-driven framework. We are transforming the research and planning processes for clinical trials by removing barriers that keep data from reaching its intended users. To achieve this, we collect vast amounts of trial-related documents from both your internal assets and the public realm, allowing you to concentrate on what truly matters—enhancing patient outcomes. By streamlining access to essential data, we empower teams to make quicker and more effective informed decisions, ultimately leading to more successful trial results in the future. This holistic approach not only improves efficiency but also fosters innovation in clinical research.

What is Cytel?

Cytel is recognized as a leading global innovator in the realm of software dedicated to clinical trial design, biometrics, and sophisticated analytics, with a goal of enhancing clinical trial efficiency while empowering pharmaceutical firms to fully leverage both clinical and real-world data. Founded in 1987 by esteemed statisticians Cyrus Mehta and Nitin Patel, Cytel has maintained its position at the forefront of adaptive clinical trial technology and biostatistics. Its flagship software, the East Horizon platform, plays a crucial role in supporting accurate trial design and simulation, utilizing adaptive and Bayesian approaches to refine protocols and streamline the drug development journey. The East Horizon platform represents a holistic integration of Cytel's trusted software solutions, boasting R integration that markedly enhances trial design capabilities. Additionally, Cytel offers the Xact software suite, an extensive toolkit tailored for statistical analysis of smaller datasets, effectively addressing challenges posed by sparse and missing data. By persistently innovating and broadening its range of products, Cytel is dedicated to delivering state-of-the-art solutions that align with the dynamic demands of clinical research, ensuring that researchers have the tools necessary to improve patient outcomes. As a result, Cytel continues to shape the future of clinical trials through its unwavering commitment to excellence in software development and analytics.

Media

Media

Integrations Supported

R

Integrations Supported

R

API Availability

Has API

API Availability

Has API

Pricing Information

$20 per 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

Trials.AI

Date Founded

2014

Company Location

United States

Company Website

trials.ai

Company Facts

Organization Name

Cytel

Date Founded

1987

Company Location

United States

Company Website

cytel.com

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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