Products

Some examples of CLARA AI Applications

We are focusing on 3 primary product applications for our technology, as well as being open to custom development.

Translate Medical ResearchTransforms technical medical research documents into readable, searchable information; formats into the assets you need to run your business.CLARA has a deep semantic understanding of clinical trial protocols, can translate complex medical study terminology from a variety of sources, and export it in any format or language.

Patient Assistant (Clara Chat)Understands and empathizes with patientsA user-friendly conversational interface provides real-time personalized support to clarify study protocols, and address user questions, expectations, and needs

Informed ConsentSpend less time on low-value research activitiesClara can quickly spin up patient facing documents for clinical trial onboarding, and generate pre-qualification and e-consent apps

Custom ApplicationsExpert guidance and analysis, tailored to your needsIn addition to our own suite of products, we have extensive experience building and shipping software applications to meet specific needs. Contact us to learn more about how we can help you!

Translation & Search

Informed Consent

Patient Assistant

Custom Applications

About CLARA

CLARA’s protocol-powered AI addresses the most pressing challenges in clinical trials by automating time-consuming tasks, ensuring accuracy and regulatory compliance, reducing costs, improving patient engagement, and accelerating trial timelines, ultimately making the entire process more efficient and streamlined. The biggest challenges in clinical trials often revolve around complexity, time, cost, and accessibility.Here’s how protocol-powered AI can address these challenges:

Challenges

The Challenges

Lengthy Start-Up Timelines
Regulatory Compliance
Inconsistent and Error-Prone Documentation
High Costs
Difficulty Recruiting and Retaining Participants
Patient Engagement and Accessibility
Data Quality and Consistency Across Teams
Slow Trial Timelines

Clinical trial start-up is often delayed due to the manual creation of key documents like IRB submissions, consent forms, translations, and patient screening questions. These tasks require a significant amount of time and coordination between multiple stakeholders.

How Protocol-Powered AI Helps

CLARA automates the generation of these documents, translating complex protocols into actionable outputs in a fraction of the time. This speeds up the trial start-up process, ensuring trials can begin sooner.

Our Solution

CLARA AI Platform

HumanTrue’s Protocol-powered AI CLARA is an artificial intelligence system specifically designed to deeply understand and process clinical trial protocols—the foundational documents that outline the objectives, methods, and details of a study.The "protocol-powered" aspect means that our AI's core function is driven by its ability to semantically interpret these protocols, transforming them into actionable and operational outputs.

Here's a breakdown of what CLARA's protocol-powered AI does:

Input: Source Content

Application accepts complex medical content, such as a trial
protocol document, NTCID, EUDRA ID etc.)

CLARA AI

Assesses and Processes

Semantic Understanding

Our AI comprehends your protocol's structure, language, and intent, making sense of the complex medical and technical information within.

Automated Document Creation

Based on its understanding of the protocol, our AI generates essential trial documents such as patient consent forms, IRB documents, screening questions, and study summaries, all aligned with the original protocol, and potential study revisions.

Process Optimization

By automating traditionally human-driven tasks, protocol-powered AI eliminates bottlenecks in trial start-up processes, ensuring that tasks like regulatory submissions and patient communications are expedited.

Personalized and Simplified Outputs

Our AI translates complex study information into simpler terms for non-experts, such as patients and clinical staff, while retaining the necessary detail for regulatory compliance and professional stakeholders.

We prioritize security, compliance, and performance.

The CLARA platform is GDPR and HIPAA compliant, and meets standards set forth by the EU and US regulatory bodies.All translation is done asynchronously and offline to deliver instant performance and fast user experience.

Our advantage over public language models

Public/free language models such as OpenAI and Google are useful tools for summarizing and interpreting of technical content, and we encourage everyone to be familiar with them. In fact, we use them too. In the clinical study environment however, accuracy and accountability matter. And the output from public language models may not be usable in many cases without significant resources dedicated to fact checking.HumanTrue’s CLARA AI is sensitive to the intricacies of the field of medical research and has deep semantic understanding of clinical trial protocols, processes, and concepts at all levels. Our unique built-in verification system reduces hallucinations and factual errors from the outset, and when questions do arise, CLARA can “show its work” for any output it generates from the original source materials.

Contact Us

How can we help you?

Email us at info@humantrue.com or send a message.