CONTROLLED
CDM INTEGRITY SYSTEMS
Clinical Research.
Connected by Design.
One ecosystem for trusted clinical research.
Clinical source, operations, regulatory processes, quality, monitoring and compliance connected through one traceable environment.
CDM INTEGRITY SYSTEMSConnected command center
ECOSYSTEM ACTIVEOPERATIONAL OVERSIGHTCDM OS ◈
CONNECTED
VERIFIED
CONNECTED ARCHITECTURE
Clinical sourceOperationsQualityEvidenceMonitoring
ACTIVITY SIGNALS
01Information is created only once.
CDM / 01One ecosystem. Endless connections.
THE FRAGMENTATION GAP
Clinical research can be digital and still remain disconnected.
Source data, spreadsheets, email, regulatory repositories, quality systems, laboratory information and monitoring often depend on manual handoffs. Each handoff creates another opportunity for duplication, transcription, reconciliation, inconsistency or omission.
01
Clinical source
02
EDC
03
Spreadsheets
04Email
05
Regulatory
06
Quality
07
Laboratory
08
Monitoring
THE CDM MODEL
One connected operating model.
A system is connected when information, actions and accountability retain context throughout the lifecycle.
One ecosystem
Research execution, integrity and oversight designed as one environment.
One data point. One source.
Information retains its origin, authorship and context.
One action feeds the next.
Operational events can move the process forward without losing traceability.
Everyone contributes. Everyone benefits.
Sites, investigators, quality teams and sponsors retain accountable roles.
CDM IN 3 MINUTES
See how one action activates the entire ecosystem.
A visual journey from clinical data to operations, control, evidence and trust.
CORPORATE VIDEO · 03:00
CDM INTEGRITY SYSTEMS
PLATFORM ARCHITECTURE
Connected around the clinical-research lifecycle.
The platform is a connected operating environment, not a shelf of unrelated applications. Specific functions remain subject to approved product scope.
EXPLORE PLATFORM ARCHITECTURE →01SOURCE
02ACTION
03CONTEXT
04REVIEW
05EVIDENCE
Conceptual data-flow representation. Detailed functions remain subject to approved product scope.
SPONSOR EXPERIENCE
Oversight without erasing site responsibility.
CDM is designed to help sponsors and CROs understand study execution through governed signals, while preserving ownership, source context and qualified human decisions.
EXPLORE SPONSORS & CROS →GOVERNED OVERSIGHT CONCEPT
Study execution
Operational signals
Quality indicators
Monitoring context
Risk & follow-up
Evidence status
Conceptual representation. No product metrics or live capabilities are asserted here.
DATA INTEGRITY
Integrity is not an inspection event.
Authorship, timestamps, source, changes, reasons, signatures and audit trail belong to the lifecycle of the record—not to a reconciliation exercise at the end.
AuthorshipTimestampSourceChangesReasonSignatureAudit trail
QUALITY BY DESIGN
Quality shouldn't begin when the monitor arrives.
Quality by design means responsibilities, controls, evidence and follow-up are embedded in how work is performed.
CDM SENTINEL
From compliance statements to compliance evidence.
CDM Integrity Systems operates the research. CDM Sentinel proves its integrity.
EXPLORE CDM SENTINEL →TRACEABLE ASSURANCE CHAIN
01REQUIREMENT
02CONTROL
03OWNER
04FREQUENCY
05EVIDENCE
06STATUS
07ALERT
08ACTION
Sentinel reports readiness, evidence and gaps. It does not by itself certify compliance.
TRUST CENTER
Trust must be inspectable.
Security, privacy, data integrity, availability, traceability, validation, auditability and resilience require evidence—not adjectives.
SPONSOR DEMO
See CDM Integrity Systems in action.
Start a focused conversation about your studies, sites, quality model and assurance priorities.
BOOK A SPONSOR DEMO →