Solutions

A product family grouped by problems, not a catalog

Every product runs on the same evidence layer: data entered once, synced in real time, traceable end-to-end.

One connected product familyFrom data capture to operational decisions, on one evidence layer
01

Clinical Data & Endpoints

EDCRTSMeCOAIRC
02

Study Operations

CTMSeTMFRM
03

Training Enablement

eLearning
ECC Connected Evidence LayerUnified identity · real-time sync · complete audit trail · controlled AI

Clinical Data & Endpoints

Connect data capture, randomization, patient outcomes, and independent review for reliable, traceable evidence.

EDC · Electronic Data Capture
AI-driven study build and OCR-assisted capture on one ALCOA+ compliant EDC platform.
Protocol-driven AI study build — 60% less effort
AI-powered OCR capture at 95% accuracy
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RTSM · Randomization and Trial Supply Management
Randomization and supply for multicenter trials — flexible designs, intelligent supply alerts.
AI one-step configuration — 10–20% less build effort
Drug lifecycle management with smart alerts
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eCOA · Electronic Clinical Outcome Assessment
Five COA dimensions on one global, multilingual platform with AI-assured capture quality.
Full coverage: ePRO, eClinRO, eObsRO, ePerfO, eDiary
AI-guided capture lifted pass rates from 40% to ~95%
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IRC · Independent Review Committee
A GxP-aligned platform unifying image upload and independent review, with expert readers.
One-stop independent review — controlled and traceable
Senior readers across oncology and beyond
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Related endpoint services: Scale Management · Linguistic Validation · Rater Training

Study Operations

Manage studies, trial master files, and research resources through connected, visible workflows.

CTMS · Clinical Trial Management System
Full-lifecycle trial management with real-time tracking, risk monitoring, and AI assistance.
One-click AI setup and natural-language analytics
RBQM ecosystem plus the ECC ONE mobile app
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eTMF · Electronic Trial Master File
AI-assisted filing and QC for the trial master file — aligned with GCP and 21 CFR Part 11.
AI classifies and files documents correctly the first time.
Upstream AI QC keeps the TMF inspection-ready
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RM · Resource Management
Contracts, people, and revenue-cost management for CROs, SMOs, and pharma — with BI built in.
Contract decomposition for precise resourcing
Transparent costs with multi-dimensional BI
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Training Enablement

Role-based learning, assessment, and qualification for study teams.

eLearning · eLearning Training Platform
Online training and LMS with targeted assignments, provable records, and rater consistency training.
Targeted assignments with end-to-end tracking
Automatic scoring and certificate generation
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Planning a regional or global study? Bring the protocol and the hard questions.

Meet with a team that combines regional delivery depth with global clinical technology standards.

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