CDM Integrity Systems — Clinical Data Management
CDM INTEGRITY SYSTEMSCONNECTED ECOSYSTEM

One ecosystem for trusted clinical research.

A connected platform concept for clinical source, study operations, regulatory processes, quality, monitoring, data integrity, documentation and governed integrations.

Contextual connection Integrity by design Governed oversight
CDMINTEGRITYSYSTEMS
Clinical source
Operations
Quality
Evidence
CDM SENTINELGoverned oversight
CONNECTED CLINICAL ARCHITECTURE
ONE ACTION · ONE ECOSYSTEM
CDM / PLATFORMWe don't just digitize clinical research. We orchestrate it.
GOVERNED EXECUTION

CONTENT ARCHITECTURE

Continue your CDM evaluation.

Select an area to review its purpose, operating model, boundaries and required evidence.

HOW IT CONNECTS

Each domain preserves context, accountability and evidence throughout the research lifecycle.

01

Clinical Source

Source context, authorship and traceability designed around the record lifecycle.

SCOPE CONFIRMATION REQUIRED

02

Study Operations

Connected responsibilities and operational actions across the research environment.

SCOPE CONFIRMATION REQUIRED

03

Quality Management

Quality responsibilities, findings, actions and evidence linked to execution.

CONCEPT SUPPORTED

04

Monitoring

Governed oversight concepts that preserve site responsibility and source context.

SCOPE CONFIRMATION REQUIRED

05

Data Integrity

Authorship, timestamps, change history, reasons, signatures and auditability.

ARCHITECTURE SUPPORTED

06

Documents & Integrations

Controlled information and event-based connections with explicit data boundaries.

INTEGRATION CONCEPT SUPPORTED

CLAIMS BOUNDARIES

Public information separates design, confirmed scope, implementation status and approved evidence. No unsupported certification or capability is presented.

Detailed product functionality will be published only after approval of the CDM Integrity Systems feature matrix.