Harnessing Clinical Trials with GenAI Companion

Step into the future of clinical trial with ClinicAI, DataArt's AI-driven solution that accelerates and optimizes the entire process. Tailored for pharmaceuticals, medical tech companies, and Contract Research Organizations (CROs), this cutting-edge tool provides care management system operators with real-time query assistance.

LocationGlobal

IndustryHealthcare Software Development

ServicesAI and ML Services

About

ClinicAI is reshaping the clinical trial landscape with an AI-driven solution that accelerates and optimizes the entire process. Tailored for pharmaceuticals, medical tech companies, and Contract Research Organizations (CROs), our solution streamlines operations by efficiently generating clinical documents, addressing queries, and conducting eligibility checks.

Challenge

Clinical trials have been burdened by manual, error-prone, laborious, and costly processes, often consuming a significant portion of the 10 to 12 years required for a drug journey from the laboratory to the pharmacy shelf. Despite significant investments of time and resources, the industry faces several persistent challenges, including:

Poor patient cohort selection
Ineffective recruiting tactics
Insufficient infrastructure

These issues not only delay the drug development process but also escalate costs and reduce overall efficiency.

Solution

DataArt developed a PoC using Google's Gemini API, integrating it with customer knowledge bases to enhance accuracy in responding to user inquiries and improving document processing and generation. The platform features an ADA-compliant interface, making it accessible without the need for specialized engineering expertise. This allows researchers and scientists to utilize the tool immediately and effectively.

Features

ClinicAI offers a range of features designed to streamline clinical trial operations:

Data Input: Researchers and clinical trial coordinators can upload patient data and clinical documents in various formats, including .pdf, .docx, etc.).
Text Conversion: The system standardizes all input data by converting it into a single text format, ensuring uniformity and consistency.
Prompt Selection: Users can select from predefined prompts to perform tasks such as:
- Summarizing study protocols
- Outlining eligibility criteria
- Generating patient consent forms
- Creating clinical trial timelines and summaries of study outcomes

Use Cases

Study Summary Generation

Crafting study summaries manually is not only time-consuming but also demands specialized expertise.
ClinicAI steps in to automate this process, delivering concise overviews of study objectives, patient eligibility, screening procedures, and key milestones.

Development of ICFs

Creating Informed Consent Forms (ICFs) can be a tedious task, often needing multiple revisions due to changes in protocols and regulations.
ClinicAI simplifies this process by drafting clear, plain-language consent forms based on study protocols, making them easily understandable for the intended audience.

Requests Management

Answering study subjects' questions involves meticulous document review and careful response formulation.
ClinicAI automates responses to common inquiries about study risks, side effects, and procedural details, improving communication with study participants.

Eligibility Check Automation

Determining patient eligibility requires thorough document review and specialized knowledge.
ClinicAI automates this process by extracting and summarizing eligibility criteria from various documents, speeding up the screening process and ensuring accurate eligibility determination.

Technological Aspects

Advanced UI/UX

ClinicAI features a seamless document-sharing system, intuitive navigation, an ADA-compliant interface, user-friendly access to commonly used requests, and generation of reports and consent forms.

AI Integration

The solution utilizes Google Cloud's Vertex AI Gemini Pro and BigQuery as core services. It provides extensive customization options to meet specific organizational needs while ensuring compliance with rigorous regulatory standards such as GDPR and HIPAA.

By harnessing the power of AI, ClinicAI transforms the clinical trial process, making it faster, more accurate, and more efficient. This innovative solution addresses the longstanding challenges of clinical trials, paving the way for quicker drug development and improved patient outcomes.

Watch the full video to see how 𝗖𝗹𝗶𝗻𝗶𝗰𝗔𝗜 can streamline your clinical trials:

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