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Development of a Real-Time Clinical Data Platform for Enhanced Research Efficiency
  1. case
  2. Development of a Real-Time Clinical Data Platform for Enhanced Research Efficiency

Development of a Real-Time Clinical Data Platform for Enhanced Research Efficiency

darly solutions
Medical
Information technology

Identified Challenges in Clinical Trial Data Management and Monitoring

The client faces difficulties in managing large volumes of sensitive patient data collected from connected medical devices during clinical trials. Existing systems lack tight integration, real-time data visualization, and secure access controls, leading to inefficiencies, potential data quality issues, and compliance risks. The need for a scalable, intuitive, and secure platform to aggregate, visualize, and analyze real-time health data is critical to enhance research productivity and data reliability.

About the Client

A mid-sized biomedical technology company specializing in medical devices and health data management solutions, aiming to streamline clinical trial data processing and analysis.

Key Goals for the Clinical Data Platform Development

  • Develop and deploy a centralized web-based platform enabling real-time monitoring, visualization, and analysis of clinical trial data to improve researcher productivity by approximately 20%.
  • Implement tools to enhance data quality and integrity, aiming for at least a 10% increase in data reliability metrics.
  • Achieve a user satisfaction rate of at least 85% among early adopters through intuitive design and usability.
  • Accelerate development timelines utilizing prebuilt UI components and modular architecture.
  • Ensure full compliance with relevant privacy, security, and regulatory standards to mitigate legal and non-compliance risks.
  • Design the system for scalability to support multiple concurrent trials without performance degradation.

Core Functional Requirements for the Clinical Data Management System

  • Real-time data aggregation and visualization dashboard showing participant metrics with trend indicators and measurement units toggle.
  • Secure user authentication and role-based access control for maintaining patient data confidentiality.
  • APIs for integration with existing backend systems to facilitate data synchronization.
  • Event-driven notifications and alerts for new data entries or transfer issues via real-time communication channels.
  • Low-latency data refresh capabilities to ensure timely updates, with an aim to reduce latency by over 40%.
  • Error handling mechanisms to prevent system interruptions and maintain data integrity during data transfer and visualization.

Technology Stack and Architectural Preferences

React for frontend UI development, leveraging component libraries for rapid deployment
RTK Query and WebSockets for real-time data streaming
Material UI for consistent, prebuilt UI components
Secure encryption protocols and access controls aligned with industry standards
Scalable cloud architecture to manage multiple simultaneous clinical trials

Essential System Integrations

  • Existing backend health data systems via RESTful APIs for data aggregation
  • Connected medical devices such as insulin pumps and sensors for direct data transmission
  • Notification systems for event-driven alerts and updates

Non-Functional System Requirements

  • High scalability to support hundreds of data updates and multiple concurrent trials
  • Performance requirements achieving near real-time data refresh with latency reduction of at least 43%
  • Strict security with data encryption and role-based access controls
  • Usability focused UI/UX design based on human-centered principles for intuitive operation
  • Regulatory compliance to ensure adherence to health data privacy standards

Expected Business Impact and Benefits of the Clinical Data Platform

The deployment of this real-time clinical data platform is projected to increase researcher productivity by approximately 21-23%, enhance data reliability by at least 10%, and reduce data monitoring time by roughly 23%. The system’s scalability and robust security will mitigate compliance risks, providing a more efficient and trustworthy environment for clinical research across multiple trials.

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