Life Sciences & Clinical Trials

The Integration Layer for
Life Sciences

Clinical trials collect data from more sources than ever — EDC systems, eCOA patient devices, lab information systems, imaging platforms, wearables, and electronic Trial Master Files. The vendor landscape is dominated by proprietary ecosystems that don't integrate well with each other. Manual data reconciliation increases trial cost and introduces errors.

Connect Your Trial Stack

The Clinical Trial Integration Problem

Running a modern trial means stitching together a fragmented vendor ecosystem under some of the strictest regulatory requirements in any industry.

Proprietary Silos

Major platforms — Medidata Rave, Veeva Vault, Oracle Clinical — lock data into proprietary ecosystems. Running a best-of-breed stack means building custom integrations between every pair of systems: EDC to CTMS, CTMS to safety, safety to regulatory.

Regulatory Complexity

FDA 21 CFR Part 11, GxP validation, ICH-GCP guidelines, and EU Clinical Trials Regulation impose strict requirements on data integrity, audit trails, and electronic records. Generic automation tools cannot meet these standards.

Multiplying Data Sources

Decentralized trials add wearables, remote monitoring, and telemedicine data streams that must flow into trial databases with full traceability. Each new data source is another integration to build and validate.

How OneHazel Solves It

AI-powered integration infrastructure purpose-built for the complexity of clinical trial data ecosystems.

AI-Powered Connector Generation

Point our AI agent swarm at any clinical trial vendor's API documentation. Seven specialized agents analyze endpoints, detect auth, generate OpenAPI specs, map to a canonical trial data model, and produce validated connectors — automatically.

Universal Gateway

One API call handles translation between your EDC, CTMS, safety database, and lab systems. Auth application, schema translation, circuit breaking, rate limiting — all managed. Your platform talks to OneHazel; we talk to every vendor in your trial stack.

Canonical Trial Data Model

Subjects, visits, adverse events, lab results, imaging data — normalized into a unified schema regardless of source system. Replace a vendor without rebuilding your data pipelines.

Event-Driven Trial Workflows

Trigger automated actions when a lab result arrives, an adverse event is reported, or a site enrollment milestone is reached. Chain operations across EDC, CTMS, and safety systems — no custom integration code.

Key Integrations

AI-generated connectors for the systems that power clinical trials, from data capture to regulatory submission.

EDC Systems

Medidata Rave
Veeva Vault EDC
Oracle Clinical One
Castor

CTMS

Medidata CTMS
Veeva Vault CTMS
Clinion

ePRO / eCOA

YPrime
Clario
Medidata Patient Cloud

Safety & Pharmacovigilance

Oracle Argus
ArisGlobal
Veeva Vault Safety

Labs

LabCorp Drug Development
ICON Central Labs

eTMF & Regulatory

Veeva Vault eTMF
Montrium
IQVIA RIM

What You Save

Replace fragile point-to-point integrations with a unified, AI-powered integration layer.

Without OneHazel

Custom integrations between each pair of trial systems

Dedicated data management team for manual reconciliation

Vendor switches require full re-validation

Months to onboard new data sources

With OneHazel

AI generates connectors from vendor API docs in minutes

One unified API replaces point-to-point integrations

Swap vendors by changing a connector — reduce re-validation scope

New data sources connected through the marketplace

Start connecting your clinical trial stack

AI-generated connectors for EDC, CTMS, safety, labs, and regulatory systems. One unified API for your entire trial data ecosystem.

<100ms
Latency Overhead
100%
Schema Abstraction
ISO/GDPR
Compliant Hub
Global
Vendor Reach

OneHazel

The Vertical iPaaS for Data Intelligence.