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Research Infrastructure, Fully Managed

We replace the fragmented tools required to run modern research programs — registries, consent systems, file storage, study workflows, and governance — inside a single compliant platform.
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Research Institutions & Academic Medical Centers

Run longitudinal cohorts on a unified platform with study-scoped consent, role-based workflows, and compliant data infrastructure — no custom engineering required.

Biobanks & Disease Foundations

Build participant-driven data ecosystems with identity management, eConsent, survey engines, and file vaults — all inside your own isolated environment.

Pharma, CROs & Hospital Networks

Manage multi-site enrollment, clinician-mediated data collection, and cross-study governance with per-tenant encryption and audit trails.

The Platform

Identity & Consent

Participant, clinician, and caregiver identity management

Registry-level and study-scoped consent with versioning

eSignature capture with audit trails

Baseline IRB-approved consent framework included

Data Infrastructure

Virtual private environment per organization

Isolated storage with dedicated encryption keys

Structured (surveys) and unstructured (files, genomics) data

Large file ingestion with chunked upload support

Study & Workflow Engine

Configurable studies with enrollment limits

Survey builder with branching logic and prerequisites

Role-based workflows (participant, clinician, caregiver)

Data tagged by participant, study, and respondent type

Governance & Compliance

HIPAA, GDPR, and NIST AI RMF aligned

Audit logs and action tracking

Participant rights: download, edit, delete, revoke

Physical and cryptographic tenant separation

How It Works

1. You Provide Your Program Details

Your branding, your surveys, your consent language, and your study structure.

2. We Configure and Deploy

A fully isolated portal instance mapped to your organization's private environment — live in weeks, not years.

3. You Launch

With a production-ready participant portal, optional clinician tooling, and a secure, compliant data backend.

Interested in becoming a DigitalCabinet Community? Send us a message!

Frequently Asked Questions

DigitalCabinet is a compliant research infrastructure platform — not just a survey tool. We provide identity and consent management, study-scoped data collection, large file handling, role-based workflows, governance tooling, and audit trails. Each organization gets its own isolated environment with dedicated encryption keys and access controls.

Just your goals. You provide your branding, surveys, consent language, and study structure. We handle hosting, security, compliance, configuration, and deployment. Most partners are live within 2–4 weeks.

Yes. Each organization gets its own virtual private environment with isolated storage, encryption keys, access controls, and origin validation. You define roles and permissions. Data access can be segmented by group, dashboard role (admin/clinician/participant), and consent tier.

We support the full spectrum. Some programs are fully self-serve — participants register, consent, and contribute data independently. Others run entirely through care teams, with clinicians enrolling participants and submitting data on their behalf. Most are somewhere in between. We support all of it.

Participants retain full rights over their data. They can download, edit, or revoke access at any time. If a participant withdraws consent, their raw data is removed — with no disruption to de-identified analysis layers.

Yes. We support upload of large files (WGS, PDFs, etc.), structured medical data (via FHIR/EHR integrations), and custom formats. Everything is stored securely in your private environment and linked to participant records with full consent governance.

DigitalCabinet is fully GDPR and HIPAA compliant, with layered encryption, role-based access, and audit trails. Your data is physically and cryptographically separated from every other program on the platform. Visit our Trust Center for more.