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eSAE

Safety Management in Clinical Trial Solution System

eSAE focuses on life-cycle SAE management from collection to archiving. It is based on one platform for SAE report management beyond safety database. Empowered by digital transformation, eSAE can reduce as much as 50% labor intensive efforts. Most important of all, it is compliant with GCP as well as GVP requirements.

01

Comply with Regulations covering SAE report life cycle 

 

Cover the collection, processing, submission, distribution, archiving and analysis of safety information in clinical trials

 

Configure with MedDRA/WHODD as the first integrated system for SAE management in clinical trials in China

02

Technology Empowers Efficiency Improvement 

 

Intelligent SAE Collection could be done within 20 min by site staff

 

SAE collection / processing / distribution / verification in one platform with auto archiving

03

Overall Quality / Risk Dashboard Visualization

 

Key Performance Indicators for assessment and decision making

 

Project level team tasks are available for performance review and compliance management

04

Comprehensive Implementation and Client Service Team

 

Provide product and services to 300+ clients worldwide

 

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