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features
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support

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Description

TrialMind serves as an AI-driven clinical research platform catering to pharmaceutical and biotechnology firms, contract research organizations, and academic medical institutions. The platform's capabilities extend to trial design, statistical programming, real-world evidence generation, cohort analysis, literature reviews, and research into the clinical trial landscape, as well as supporting clinical operations. Its workflows encompass various essential processes such as site selection, matching patients to trials, refining eligibility criteria, forecasting enrollment and dropout rates, and conducting data and medical monitoring. Users can articulate their tasks using natural language, examine analysis plans, and review findings with connections to relevant sources, methodologies, and code. TrialMind is available in multiple formats, including hosted software, private cloud solutions, or deployment directly within a client's infrastructure. Importantly, raw patient records remain within the customer’s environment throughout the matching process, ensuring data privacy. Additionally, API and Model Context Protocol access facilitate the integration of its functionalities into other platforms, enhancing usability and efficiency. This comprehensive approach empowers research teams to streamline their clinical trials effectively.

Description

Our innovative Smart Protocol system is designed to infuse automation and intelligence into the design of clinical trials using artificial intelligence. This groundbreaking solution is transforming the traditional manual processes that research teams have relied on to create clinical trials. In today’s digital landscape, it is practically impossible for individuals to thoroughly analyze every detail pertinent to a decision. Furthermore, many organizations possess valuable data that often goes untapped, with documents frequently stored in repositories that lack visibility. Consequently, life science companies may find themselves making significant and expensive choices based on insufficient information. Our goal is to transition organizations like yours from a document-centric approach to a more insightful, data-driven methodology. We are redefining the research and planning of clinical trials by eliminating the obstacles that separate data from its end-users. To facilitate this, we gather extensive amounts of trial-related documents from both your resources and the public domain, so you can focus on what truly matters—delivering better outcomes for patients. By streamlining access to critical data, we empower teams to make informed decisions faster and more effectively.

API Access

Has API Yes 

API Access

Has API No 

Screenshots View All

Screenshots View All

Integrations

Model Context Protocol (MCP) Yes 

Integrations

Model Context Protocol (MCP) No 

Pricing Details

$500/user/month
$500 per user per month.
Free Trial No 
Free Version No 

Pricing Details

$20 per month
Free Trial No 
Free Version No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Deployment

Web-Based Yes 
On-Premises No 
iPhone App No 
iPad App No 
Android App No 
Windows No 
Mac No 
Linux No 
Chromebook No 

Customer Support

Business Hours Yes 
Live Rep (24/7) No 
Online Support No 

Customer Support

Business Hours Yes 
Live Rep (24/7) Yes 
Online Support Yes 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person No 

Types of Training

Training Docs Yes 
Webinars Yes 
Live Training (Online) Yes 
In Person Yes 

Vendor Details

Company Name

Keiji AI, Inc.

Founded

2023

Country

United States

Website

keiji.ai

Vendor Details

Company Name

Trials.AI

Founded

2014

Country

United States

Website

trials.ai

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance No 
Document Management No 
Electronic Data Capture No 
Enrollment Management No 
HIPAA Compliant No 
Monitoring No 
Patient Database No 
Recruiting Management No 
Scheduling No 
Study Planning No 

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance Yes 
Document Management Yes 
Electronic Data Capture Yes 
Enrollment Management Yes 
HIPAA Compliant Yes 
Monitoring Yes 
Patient Database Yes 
Recruiting Management No 
Scheduling Yes 
Study Planning Yes 

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