Egnyte for
Life Sciences eTMF

etmf dashboard showing study configuration

Reduce the administrative burden of
operating an eTMF

Collect, store, and archive study data in a secure and compliant repository with AI to automate tedious tasks.

Egnyte for Life Sciences enables the assembly of eTMFs on a GCP-compliant platform. ​​We give you the tools to ensure data integrity, meeting 21 CFR Part 11 requirements (audit trails, checksums, and e-signatures) for collection, storage, and archiving of clinical data and regulated documents. Backed by proven AI and ML, the platform can alert you to misclassified documents, sensitive information like PHI, and suspicious activity and cyberattacks. The flexibility of the platform conforms to your workflows, whether you are starting from the DIA reference model template or have developed a highly customized structure from scratch.

video on hosting electronic trial master files and CRO collaboration

Hosting eTMFs &
CRO Collaboration

See how easy it is to set up an eTMF structure on the Egnyte platform, and learn about the different ways Egnyte can accelerate data collection from internal and external partners through innovative collaboration features.

Over 600 Life Sciences Customers
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Trusted by Over 16,000 Businesses Worldwide

eTMF Made Easy

Smarter Data Collection

From CRFs to DICOM imagery, Egnyte collects data from internal and external partners, giving you a single, centralized repository for your study.

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Easy to Get up and Running

Built-in templates and common roles and permissions make setting up a GxP-compliant environment to host your clinical data easy.

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Automated Compliance

Egnyte’s GCP-compliant platform automates compliance, removing bottlenecks and manual processes from impacting timelines.

GXP compliance portal

Smarter Data Collection

From CRFs to DICOM imagery, Egnyte collects data from internal and external partners, giving you a single, centralized repository for your study.

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Egnyte was Ranked #1 for Data
Security by G2

From a Single Platform, Egnyte Enables

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Additional Resources

Governance Guide

GxP Buyer’s Guide

GxP Document Management for Life Sciences

White Paper

Best Practices for an Effective Quality Documentation Process

We chronicle the nine elements to keep pace with the speed of discovery

Webinar

GxP Audit Trails for FDA Compliance

Egnyte for Life Sciences platform overview focusing on audit trails, versioning, and reporting capabilities

Get Started with Egnyte Today