Aurora Yaocheng operates the AuroraPrime platform, which provides a suite of integrated tools for managing the entire lifecycle of clinical research documentation and data collection. The platform addresses inefficiencies in clinical trial processes by automating protocol design, data standardization, and compliance management, thereby accelerating the time to market for life sciences innovations.
Funding
Funding not disclosed
Founders
Product
Problem
Clinical research processes often suffer from inefficiencies in documentation, data collection, and compliance management, leading to delays in bringing life science innovations to market. Traditional methods lack integrated tools for managing the entire clinical trial lifecycle, hindering automation and standardization.
Solution
Aurora Yaocheng's AuroraPrime platform offers a suite of interconnected modules designed to streamline and manage the complete clinical research lifecycle. The platform facilitates the digitalization of clinical research document generation and management, enhancing the efficiency of clinical trial data collection and application. By automating protocol design, data standardization, and compliance management, AuroraPrime enables life science companies to accelerate their research and development processes, ultimately reducing the time it takes to bring new products to market. The system's open architecture also supports personalized system connections, aligning with user habits and standard operating procedures.
Target Audience
The primary target audience includes pharmaceutical, medical device, and consumer health companies seeking to streamline clinical research, improve data quality, and accelerate product development.
Features
- Integrated modules for protocol writing, database building, data collection, randomization, and drug supply management.
- Support for decentralized clinical trials (DCT), biostatistics, and clinical study report (CSR) generation.
- Low-code clinical operations management platform with multiple templates and workflows.
- Electronic Data Capture (EDC) system integrated with a randomization and trial supply management system (RTSM).
- Built-in clinical logic engine and insights network.
- Capabilities for remote intelligent clinical trials.
- Solutions for automating database construction from clinical trial protocols.