Part of Our Complete
Life Sciences Suite

From lab to submission, Egnyte provides a cohesive platform for managing data, documents, and collaboration across research, clinical, and regulatory workflows.


Why Life Sciences Teams
Choose Egnyte

Egnyte enables life sciences R&D teams to accelerate discovery while 
safeguarding data—across internal teams, external partners, and 
evolving global regulatory environments.

Egnyte workspace document request analytics

Built for Omics Files and Collaborative Analysis

Accelerate genomic and proteomic discoveries with secure, searchable, and shareable access to massive omics datasets and annotated results.


Capabilities:
  • Centralized access to data across research teams
  • Metadata tagging for easier experiment tracking
  • High-speed uploads and downloads for large datasets
 
Egnyte clinical trial artifacts milestone tracker

Built for Lab Files and Structured Collaboration

Simplify cross-functional R&D by enabling real-time access to instrument output files, lab notebooks, and experiment results.


Capabilities:
  • Smart upload from lab equipment or mobile devices
  • Version control and comment threading for research files
  • Secure access for CROs and academic partners
Egnyte folder permissions file reports panel

Built for Protocols and Document Versioning

Maintain clarity and control over evolving SOPs, protocols, and project documentation—no matter how many collaborators are involved.


Capabilities:
  • Granular permissioning by folder or document
  • Automated version history and change tracking
  • Real-time co-editing with Microsoft 365 or Google Workspace
Egnyte production qualification validation reports

Built for Preclinical Data and Regulatory Readiness

Ensure preclinical data is traceable, secure, and audit-ready—from initial hypothesis through IND-enabling studies.


Capabilities:
  • 21 CFR Part 11-compliant e-signature workflows
  • Full audit trails with immutable activity logs
  • GxP-compliant storage for raw and derived data

How Life Sciences
Teams Work With Egnyte

Streamline scientific collaboration with end-to-end governance.

Lab-To-Cloud Access

Lab-To-Cloud Access

Give researchers access to real-time experimental data, lab results, and shared folders with centralized permissions and metadata tagging.
ExternalCollaboration

External Collaboration

Securely exchange data with CROs, CDMOs, and university partners via governed portals and watermarking.
Audit Readiness

Audit Readiness

Maintain traceability and audit trails across scientific workflows to ensure ALCOA+ and GxP compliance.

Built for Life Sciences Compliance
and Security Requirements

GxP Content Controls

  • Audit-Ready Trials

    Audit-Ready Trials

    Track every action for inspection readiness and regulatory compliance.
  • Granular Permissions

    Granular Permissions

    Limit folder and document access by role, site, or study milestone.
  • Automated Workflows

    Automated Workflows

    Enforce review, approval, and release for controlled documents.

21 CFR Part 11 Compliance

  • E-Signature Support

    E-Signature Support

    Capture and manage electronic signatures per FDA guidelines.
  • Version Control

    Version Control

    Maintain strict control over revisions of regulated documents.
  • Controlled Record Retention

    Controlled Record Retention

    Maintain required document histories with validated storage policies.

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How can R&D teams automate data transfer from lab instruments into a centralized, secure repository?

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How can R&D teams automate data transfer from lab instruments into a centralized, secure repository?

Egnyte lets teams map lab computers directly to secure cloud folders, so data from instruments is uploaded automatically as it's generated — no manual transfers or USB drives required. MOMA Therapeutics used this approach to connect 16 lab instruments directly to secure Egnyte folders, making data immediately accessible to scientists and automatically captured in an auditable record.

How do life sciences companies securely share research data with CROs and external partners?

Egnyte provides governed external portals where CROs, CDMOs, and university partners can upload or access files in precisely scoped folders — and nothing beyond. Watermarking, role-based access controls, and full audit trails ensure every file interaction is logged. Nimbus Therapeutics automated CRO data ingestion using this approach, loading over 99% of incoming CRO data automatically and reducing their manual data processing team from three to one.

What does a 21 CFR Part 11 compliant document management system require for R&D workflows?

A compliant system must support FDA-aligned electronic signatures, strict version control over regulated documents, and validated storage policies for controlled record retention. Egnyte delivers all three — eSignature workflows capture and manage approvals per FDA guidelines, immutable version histories prevent unauthorized changes, and configurable retention policies maintain required document histories without manual intervention or custom development.

How do biotech and pharma R&D teams stay audit-ready for GxP inspections?

Egnyte enforces GxP readiness continuously rather than as a pre-audit scramble. Granular permissions limit access by role, site, or study milestone. Automated workflows enforce review, approval, and release for controlled documents. Every file action generates an immutable audit trail that satisfies ALCOA+ requirements — so inspection readiness is built into daily R&D operations, not assembled under deadline pressure.

How can life sciences teams manage and share large genomic or omics datasets securely?

Egnyte is built for the high-volume, complex files common in genomics and proteomics research — supporting high-speed uploads and downloads for massive datasets alongside metadata tagging for experiment tracking. Teams can provide centralized, searchable access across internal researchers and share annotated omics data with CROs or academic collaborators under tightly scoped access controls, without sacrificing performance or compliance.

What's the best approach to version control for SOPs and research protocols with multiple collaborators?

Egnyte applies automated version history and change tracking to protocols, SOPs, and project documentation so every collaborator always works from the current version. Granular folder and document permissions control who can edit, comment, or view at each stage. Real-time co-editing integrates directly with Microsoft 365 and Google Workspace — eliminating the version confusion and email-based reconciliation that slow protocol-heavy R&D teams.

How do R&D organizations protect intellectual property when collaborating with external partners?

Egnyte scopes external access precisely — a CRO can manage files in their designated folder and nothing beyond. Watermarking on downloaded files, role-based permissions, and governed external portals ensure IP boundaries are enforced technically, not just by policy. Every file interaction is captured in a full audit trail, giving research organizations the visibility to detect and respond to any unauthorized access or data movement.

Accelerate Scientific Collaboration
and Compliance

Explore how Egnyte supports R&D data integrity, IP protection, and faster time-to-insight.