At a time when the boundaries between IT and biotechnology are blurring, ComData is introducing AI. ZET Clinical Trials Suite – a suite of AI tools that accelerates the preparation, analysis and validation of clinical studies.
This innovative AI solution works on your server, keeping data confidential, and is designed to work entirely within the Microsoft Office environment, as a set of AI Word and Excel plugins, enabling intuitive use without the need for additional training or changing work habits.
- The ZET Clinical Trials Suite is designed for clinical research organizations, pharmaceutical R&D teams, compliance and data protection departments, as well as medical database analysts.
The goal is clear — to reduce the time required for analysis and preparation of documentation from a few weeks to just a few hours, with a higher level of accuracy and full compliance with regulatory requirements.
AI.ZET Suite includes four key modules:
- Feasibility / Eligibility module – an AI assistant that analyzes complex clinical protocols, legal regulations and criteria for conducting a study. By analyzing the inclusion and exclusion criteria, it speeds up the evaluation of feasibility and increases accuracy in patient selection, thereby significantly speeding up the process of planning and conducting clinical studies.
- Text Redactor – an intelligent system for automatic removal of confidential information from documents in accordance with GDPR and EU CTR regulations.
- Patients Data Analyzer – an advanced Excel add-in that performs verification and analysis of study data against defined protocol rules.
By combining AI precision, fast integration, and scalable architecture, AI. ZET enables organizations to accelerate decision-making, improve data quality, and minimize risk.
On a technical level, the system is based on the .NET Web API, PostgreSQL database, microservice architecture with Docker containers and locally implemented LLM models that guarantee complete control over the data. All processes take place within the client's secure environment, with VPN access, encrypted file storage, and full compliance with GDPR, HIPAA, and ISO/IEC 27001 standards.
The result is a solution that connects the worlds of IT, biotechnology, and medicine, bringing new efficiencies to clinical research — where precision, quality, trust, and speed are key to advancing medicine.
