DATA, TECHNOLOGY & ANALYTICS

Clinical Data, Statistics & Technology

Connected Across the Study

CEBIS supports clinical research programs with data management, biostatistics, statistical programming and clinical technology services designed to support accurate data collection, review, analysis and study delivery.

Services can be used individually or coordinated with clinical operations and other development functions.

CORE SERVICES

Data and Technology

Across the Clinical Study

Data Management

Study build, data-management planning, CRF/eCRF support, data review, cleaning, reconciliation, database lock, export and archiving.

Biostatistics & Statistical Programming

Statistical planning, analysis, programming, interpretation and reporting aligned with study objectives.

EDC, IRT & Clinical Technology

Technology capabilities supporting electronic data capture, randomization, site management, clinical supply and broader study administration.

DATA LIFECYCLE

A Connected

Data Workflow

CEBIS supports clinical data workflows from study build and data standardization through cleaning, analysis, database lock and export.

Study Build

Configure the study and data structures around protocol requirements.

Data Capture

Collect study information through CRFs/eCRFs and supporting systems.

Data Review

Review study information and identify incomplete or inconsistent data.

Cleaning & Reconciliation

Resolve discrepancies and align relevant clinical and safety information.

Database Lock

Complete final review and prepare the study database for analysis.

Analysis & Reporting

Use statistical analysis and programming to support interpretation and study outputs.

CLINICAL DATA CAPTURE

Structured Data Collection
Throughout the Study

EDC/eCRF systems support structured collection and review of study data throughout the clinical trial.

Capabilities can include:

Study database configuration
eCRF design
Programmed edit checks
Data validation
Source-data review support
Query management
Study-data extraction

IRT & RANDOMIZATION

Connecting Participants,

Sites and Study Supply

IRT can coordinate participant, site and investigational-product activities within the study workflow. Support can include:

Participant Management

Support study enrollment and randomization requirements.

Site Management

Maintain study-site information and status.

Randomization

Support allocation based on the study design.

Clinical Supply

Connect participant and site activity to investigational-product supply needs.

DATA QUALITY

Processes Designed Around

Complete and Usable Study Data

Good study data depends on clear planning, structured collection, timely review and controlled preparation for analysis. CEBIS supports data-management planning, database design, CRF guidance, reconciliation, validation and quality-control activities across that workflow.

CONNECTED STUDY DELIVERY

Technology as Part of
the Study Workflow

Clinical technology should support the study rather than operate as an isolated system.

Clinical technology can support site management, data capture, randomization, clinical supply and study administration. Centralized study information, reusable master data and role-based access can also support study teams.

Connected areas can include:

Clinical Operations
Site Management
Data Management
Randomization
Clinical Supply
Project Management
Study Reporting

Need Data, Statistical or Clinical Technology Support?

Tell us about your study, data requirements, systems, statistical needs and expected timeline. A member of the CEBIS team can discuss the appropriate combination of services.