Egnyte for Life Sciences

Streamline eTMF Management

Inspection-ready eTMF for clinical trials.

eTMF Made Easy for Biotechs

Assemble all critical trial documents in a cloud-based document management system that grants visibility into trial completeness, quality, and timelines, with built-in audit-readiness for regulatory review. Reduce the time spent on administration of site documentation, searching for and organizing documents, and submission preparation.

Rapid Deployment

Minimize time-to-value with quick and easy set up

Inspection Ready

Ensure all documents are present and accurate with QC reviews and dashboards

Unified Clinical Ops

Leverage the full power of Egnyte’s GxP platform

The Egnyte Solution

Maintain Compliance

Stay inspection-ready with TMF completeness metrics
Support inspections with read-only inspector access
Manage all TMF documents in a GxP-compliant eTMF system

Consolidate Clinical Trial Data

Collect data across study sites and from sources such an eISF or CTMS
Centralize data from ongoing and completed studies
Maintain study data in a secure centralized repository

Leverage Actionable Insights

Monitor study completeness, timeliness and quality in real-time using the study dashboard
Conduct quality assessments throughout each study
Export inspection-ready inventory and completeness reports

The Power of Many Solutions In One Turnkey Platform

Egnyte’s modular offerings grow with your company through all development and approval phases - from startup to scale up.

GxP Compliance Portal
Rapid Validation
Audit Trails
Multi-Step Workflows
Data Lifecycle Management

CDISC TMF Reference Model
Unified Dashboard
Milestone Management and Reporting
Multi-version Upload

Over 600 Life Sciences Customers Trust Egnyte

Egnyte’s eTMF is a fast, secure, CFR Part 11 compliant solution that’s perfect for the small to mid-sized biotechs we work with. It allows us to empower our clients with the best technology for their early-phase trials.

Andrew Brackin

Co-Founder, Vial

Read Case Study

We’re able to manage each document much more efficiently, and when you multiply those efficiencies by the thousands of documents in a typical trial, it adds up... We now move 30% faster on key tasks like storing documents, quality checks, reporting, and many others.