Data-Driven Studies: Faster and smarter results delivered.

Own Your Data Relationship

Power your next study with Axiom’s Fusion eClinical Suite and DM/PV/BioStats Services, the most configurable unified eClinical solution dedicated to small to medium sized pharma, biotech, medical device companies, and CROs worldwide.

Standard Trials | Virtual Trials | Remote Trials | Home Healthcare Supported Trials

Data Management | Data Analytics | Pharmacovigilance | BioStats

Fusion eClinical Suite Logo

Fusion brings together over 15 fully integrated modules that connect seamlessly on one unified platform.

Get single log-on access to all of your study data and real-time alerts delivered to your device of choice, so you can make informed decisions, faster.

Axiom’s technology and services eliminate the labor intensive manual tasks so often required by smaller companies in managing a clinical study or study platform.

Fusion eClinical Suite modules list
REPORTING TOOLS: Patient Profile Reports, Response Tracking, Assessment Reports, Lab Listings, AE/SAE Listings, Enrollment Forecasting/KPIs, Biomarker Reports

UNIFIED MODULES: CTM Tracking, Randomization, IRT/Predictive Re-Supply, Central Lab Import, AE/SAE Module, Safety Module, CTMS Module

MODULE REPORTS: IP Lifecycle Report, Case Narrative Listings, SAE Management, Enrollment Tracking, Data Dashboards

SERVICES: Data Management, Pharmacovigilance, Clinical Science, Project Management, Medical Monitoring

KEY DATA POINTS: Patient Profile Reports, Biomarker Tracking, Response Assessments

Learn how Axiom can help with your BioTech Study

REPORTING TOOLS: Patient Profile Reports, Adjudication Management, Image Oversight, Lab Listings, AE/SAE/SADE Listings, Enrollment Forecasting/KPIs

UNIFIED MODULES: CTM Tracking, Adjudication, IRT/Predictive Re-Supply, Image Import, AE/SAE/SADE Module, Safety Module, CTMS Module, ePRO, Randomization

MODULE REPORTS: Hand-Carry Tracking, Case Narrative Listings, SAE/SADE Management, Enrollment Tracking, Data Dashboards

SERVICES: Data Management, Pharmacovigilance, Clinical Science, Project Management, Medical Monitoring

KEY ASPECTS: Hand-Carry Management, Adjudication Oversight, Adjudicator Resourcing Tools

Learn how Axiom can help with your Device Study

Remote / Virtual Trials

Find out how Axiom can help bring your trial to the Patient.

ePRO / eSource

Connect with your Patients through Fusion’s ePRO app and Patient Portal.


Randomization management and reporting controlled via single platform.

Driving Innovation
Global Studies
Powered by Fusion
Experience in
Therapeutic Areas
in Largest Randomized Trial

Deliver your studies faster, easier, and smarter with Axiom as your embedded partner.

From small Phase I studies, to global trials and registries, Axiom delivers 360 degree eClinical solutions and services to meet your clinical research needs. Connect with us to learn how we help you deliver your studies faster, easier and smarter.

Explore Axiom's Professional Services

Your study is unique. Choose only the modules you need.

Fair, transparent pricing. No surprises, no hassles. Value for your investment.

With Axiom’s Fusion eClinical Suite, you can add-on any Modules to meet your study requirements. Running a small study? Just choose the base configuration with EDC, DM and AE/SAE Tracking. Running something more complex? Include powerful Modules such as Drug/Device Tracking, IWRS, Safety Management to make the management of your study so much easier.

Axiom is a Proud Member of:

“We received a quote for stand-alone EDC from a large technology vendor and were shocked. With Axiom we could resource our entire project – EDC, DM, safety, randomization, drug supply tracking and more – for significantly less that they quoted for data capture only. Our decision was easy.”Clinical Director, Boston-based biotech
“Axiom delivers the complete package for our device studies, eCRF design, EDC/DM solutions and services, real-time reporting, SAE/MedWatch forms generation, device supply and accountability and CEC/DSMB reporting. Thousands of hours saved over 12 months. A pleasure to work with.”Clinical Trials Manager, San Diego-based Device Firm

Why work with Axiom?

Know More. Know It Sooner. Act Faster.

Technology should empower you to know more, know it sooner, and act faster. That’s what good technology does.

75+ Real-Time PM Reports

Live access to clinical data reports, DSMB reporting and data listings. Getting access to the status of your study shouldn’t require a PhD in computer science. Real-time study reports in 2 clicks.

Stop Manual Reconciliation

Axiom’s unified eClinical solutions means your EDC, Randomization, Drug / Device Tracking,
Adjudication, Imaging and SAE / Safety data is in the same place.

Real-Time Study Activity Notifications

Key notifications about all of the information progress and issues within your study delivered 24/7 to your smartphone or e-mail.

Single Log-On Access

Manage safety events in Fusion, no need for a separate safety database. How about managing your AE / SAEs / SADEs and overall safety reporting from within Fusion? Track events. Create narratives.

Integrated IWRS & Randomization

Fully manage your randomization within Fusion eClinical Suite. No need to configure a separate randomization system. Fully integrated with Inventory Management for complete digital management of your IWRS/Inventory.

Drug / Device Supply Throughout Your Study

Global awareness of inventory activities, balances, and issues as well as notifications of key events including inventory levels, shipments, requests and pending activities. Stop managing your drug or device accountability in multiple systems.

“Start with the end in mind.”

One of the keys to study success is the focus of the organization on the study details, consideration for planning and strategic thinking that goes into the initiation of the study. Axiom’s Think / Deploy / Launch process ensures that a well thought-out process is the basis for planning your study.

Dedicated Customer Care

Axiom’s Customer Care team are extremely focused on ensuring that every single user in the study chain is supported throughout the entire study. Great support is linked to high-quality data. Support personnel who actually are trained on your study’s eCRF. Quick answers to end-user questions means that the study moves along quickly and efficiently.

Value for Your Investment

Expanding the technology footprint could cost more in the short term, but can greatly enhance the overall study, your real-time knowledge, key business decisions and lower costs in the long term.