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.
Comply with Regulations covering SAE report life cycleÂ
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Cover the collection, processing, submission, distribution, archiving and analysis of safety information in clinical trials
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Configure with MedDRA/WHODD as the first integrated system for SAE management in clinical trials in China
Technology Empowers Efficiency ImprovementÂ
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Intelligent SAE Collection could be done within 20 min by site staff
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SAE collection / processing / distribution / verification in one platform with auto archiving
Overall Quality / Risk Dashboard Visualization
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Key Performance Indicators for assessment and decision making
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Project level team tasks are available for performance review and compliance management
Comprehensive Implementation and Client Service Team
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Provide product and services to 300+ clients worldwide
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Comprehensive post sales service system with quick response
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