Accelerate Clinical Trials
Streamline clinical trial data management and maintain inspection readiness across trial sites and CROs.
Streamline Trial Operations With
End-to-End Governance
Accelerate study startup and execution and maintain compliance with Egnyte’s
simplified solutions for trial data management.
simplified solutions for trial data management.
Simplify Clinical Trial Data: From eTMF Management to Analysis and Governance
Inspection-Ready eTMF Management
- Automated eTMF workflows streamline document collection and filing
- Real-time tracking of essential document completeness and quality
- Integrated site and CRO collaboration within your eTMF
- Inspection-ready TMF with comprehensive audit trail monitoring
Fast and Accurate Statistical Data Analysis
- Secure validated storage environment for statistical analysis files
- Streamlined collaboration between biostatisticians and research teams
- Multilingual support for SAS, R, and Python
- Automated audit trails for statistical computing workflows
Comprehensive Data Governance
- Granular access controls for trial data
- Secure external collaboration tools
- End-to-end encryption
- Built-in GxP and ICH E6 (R3) compliance
Integration With Leading
Life Sciences Applications
Egnyte integrates seamlessly with your systems, making it easy to manage, collaborate on, and maintain compliance.
Over 600 Life Sciences Customers Trust Egnyte
"If you need a one-stop simple solution...that meets the health authorities’ expectations for a 21 CFR part 11 compliant system, and that your management isn't going to have a heart attack when they see the budget, Egnyte is definitely a good option."
Access control is crucial when working with multiple external partners….We can make sure a CRO can manage their own files and have access to the files they need to perform their tasks."
The Egnyte team spent significant time to understand our data flow processes and assist us in developing the appropriate policies.”
