AI-POWERED CLINICAL DATA CAPTURE

Making Clinical Data CaptureSimpler and More Efficient

RemoData is an intelligent clinical data capture and management system developed by LONSCIENCE for post-marketing clinical studies and real-world studies. Combining OCR and AI-powered natural language processing, it identifies laboratory reports, medical records, imaging reports and other medical documents captured using a mobile device, and supports data de-identification, parsing and automated eCRF completion.

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RemoData System Demonstration

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INTELLIGENT WORKFLOW

Intelligent Clinical Data Workflow

From multi-source data capture and OCR recognition to de-identification, intelligent data entry, AI-assisted initial review, human review and medical assessment, followed by data storage and export.

01

Data Capture

Efficient multi-source data captureStructured organization

02

OCR Recognition

Intelligent text recognitionMore efficient data entry

03

Data De-identification

De-identification of sensitive informationData security and compliance

04

Intelligent Data Entry

AI-enabled structured data entryAccurate and efficient processing

05

AI-Assisted Initial Review

Automated validation and checkingIdentification of anomalous data

06

Human Review and Medical Assessment

Human confirmationMedical assessment

07

Data Storage and Export

Export-ready dataStatistical analysis

CORE OUTCOMES

Core Performance Data

8xLaboratory report processing efficiency
6.7×Unstructured medical-record processing efficiency
>95%AI-assisted initial screening accuracy
100%Key-data confirmation after AI and human review

QUALITY & COMPLIANCE

Quality and Compliance Safeguards

AI Screening + Human Review

Automated recognition and human confirmation support the quality of key data.

End-to-End Audit Trail

Capture, processing, modification and output activities are recorded.

MLPS Assessment

Cybersecurity protection construction and assessment are conducted within the applicable scope.

Servers in China

Relevant data is stored on servers in China according to the deployment plan.

APPLICATIONS

Diverse Clinical Research Applications

Compliance-Oriented Research

Supporting studies that require standardized data management and end-to-end process traceability.

Real-World Evidence Generation

Supporting the capture, organization and analysis of real-world data.

Drug Safety Signal Monitoring

Supporting the continuous collection and processing of post-marketing safety information.

Exploration of New Uses and Patient Populations

Providing data support for research into new uses and specific patient populations.

Early-Stage Pipeline Planning

Building structured clinical information to support early-stage research decisions.

DELIVERY

Five-Step Standardized Project Delivery

01

Needs Assessment

Understand the study objectives, site scale, data sources and delivery requirements.

02

Solution Configuration

Configure study fields, eCRF forms, data rules and project permissions.

03

System Deployment and Validation

Complete system configuration, testing and the required pre-launch validation.

04

Training and Project Launch

Provide user training and support the launch of the research project.

05

Ongoing Support and Delivery

Provide system maintenance, data management, statistical analysis and project support.

SERVICES

Our Services

SYSTEM SERVICES

System Services

System Configuration and Deployment

User Training

Technical Support

System Maintenance

RESEARCH SERVICES

Research Services

Medical Writing

Data Management

Statistical Analysis

Centralized Review

Other Value-Added CRO Services