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创达EDC数据源采集录入系统

Name: 创达EDC数据源采集录入系统
Availability: InStock
Rating: 4.57 (1 reviews)

Streamline 21 CFR Part 11 compliance with AI-powered OCR recognition, voice analysis, and ICH-GCP standard workflows for high-quality clinical trial execution.

Key Figures

Downloads

User Rating

4.6/5

Total Ratings

Publisher

Chuang Da medical science and Technology (Shanghai) Co., Ltd.

Clinical Excellence Through Precision Data

A professional-grade EDC solution designed to streamline clinical trial management with AI-driven capture and global regulatory compliance.

Full Regulatory Compliance

Built-in alignment with FDA 21 CFR Part 11 and ICH-GCP standards to ensure your trial data remains audit-ready and legally sound.

AI-Powered Data Capture

Reduce manual entry errors with OCR scanning and voice analysis, digitizing source documents directly from your iPhone or iPad.

The following screenshots and description are sourced directly from the app's official store listing and are the property of the app developer.

App Store

Screenshots

创达EDC数据源采集录入系统 - Mobile interface of Trial Data EDC showing a clinical trial patient list and project details. — Mobile interface of Trial Data EDC showing a clinical trial patient list and project details.

Description

Trial Data EDC-满足法规要求的专业EDC系统，提供高质量的EDC相关服务。 Trial Data EDC: 遵循法规指南：遵循ICH-GCP,21CRF Part 11,临床试验的电子数据采集（EDC）技术指导原则等法规指南，保证EDC系统规范性。新模式及特色：数据源拍照上传，OCR识别，文本挖掘，语音分析，保证临床试验数据的完整性、准确性和真实性。数据录入：实现CRF数据的远程录入和自动化质量控制。课题管理模块：进展报告，文档管理，培训管理，风险管理模块为临床试验提高效率患者管理模块：建立高效线上随访流程，患者可及时收到随访提醒，有效提高随访的依从性并减少患者脱落率。系统同时可以进行问卷量表推送，患者可在微信端进行填写提交。并且，微信端支持患者在研究过程中随时记录不良事件、合并用药、患者病情日志等信息，有效避免患者随访期间关键信息缺失。每次电话随访过程录音并上传至云端。提高研究者或CRC电话随访的效率标准医学编码词典：MedDRA 21.0 English/ Chinese、WHODrug global B3/C3…… Trial Data EDC致力于为您提供更优质的服务