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features
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support

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Description

Antidote serves as a recruitment platform for clinical trials, enhancing the speed of medical research by connecting patients with sponsors through targeted recruitment services and a user-friendly matching search engine. Addressing the challenge that more than 80% of clinical trials face delays due to participant shortages, Antidote equips sponsors with a vendor-neutral, centralized dashboard that streamlines referrals from any source, automates the outreach process for due diligence and owner letters, monitors enrollment and return on investment metrics in real-time, and offers insightful analytics on sites and candidates with updates every hour. For patients, Antidote's intelligent matching system simplifies the intricate inclusion and exclusion criteria into straightforward guided Q&A interactions, subsequently providing current listings of clinical trials and personalized notifications for new opportunities that match their profiles. The platform is designed to accommodate both bulk and individual record imports with automated validations, and it features user-friendly, multilingual interfaces that are optimized for mobile use. This innovative approach not only enhances the recruitment process but also fosters a more effective collaboration between researchers and potential participants.

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.

API Access

Has API No 

API Access

Has API Yes 

Screenshots View All

Screenshots View All

Integrations

Model Context Protocol (MCP) No 

Integrations

Model Context Protocol (MCP) Yes 

Pricing Details

No price information available.
Free Trial No 
Free Version No 

Pricing Details

$500/user/month
$500 per user 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 Yes 

Customer Support

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

Types of Training

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

Types of Training

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

Vendor Details

Company Name

Antidote

Founded

2010

Country

United States

Website

www.antidote.me/

Vendor Details

Company Name

Keiji AI, Inc.

Founded

2023

Country

United States

Website

keiji.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 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 

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