Clinical Trial Software for Site Networks

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CROs

Patient Management

Streamlined Scalability for Multi-Site Success

Decentralized site networks need trial management that adjusts to their specialized communication, oversight, and team collaboration needs. CCTrialSuite empowers site networks to adapt to the ever- changing research environment and scale their business accordingly 

Why CCTrialSuite for Site Networks?

Faster Enrollment

Flexible Configuration

Enables network-wide distribution of standardized study protocols in real time.

Increased Profitability

Financial Management

Ensures network-wide financial, research, and management procedures and compliance.

Streamlined Communication

Enhanced Communication

Facilitates faster, more reliable communication within and beyond the site network.

Tablet

Easy eCRFs

Use eSource smart forms and standard workflows to capture visit data digitally and cut out slow double data entry.

Data Management

Advanced eRegulatory

Simple, compliant, secure eBinder and regulatory document management for all your studies.

Standardized Compliance

Project Management

Includes best-in-class project management tools.

Clinical Trial Software for Site Networks

Clinical research management system for single sites and enterprises.

The industry’s most complete CTMS-EDC integration.

The industry’s most advanced patient payment application.

Text messaging solution designed to boost patient engagement and retention.

Capture source data in real time, enhance data quality and optimize site operations.

Efficient document management system for managing complex regulatory requirements.

The only electronic consenting system for sites that keeps patients engaged, ensures participant understanding, simplifies oversight and improves the overall consenting process.

What Clinical Research Organizations Are Saying

Davita
Case Study

“Because we were running 150 trials, DaVita wanted to make sure that we could keep track of reporting metrics in one central location.”

Linical Accelovance
Case Study

“We now have clear, complete, and timely data showing us exactly how well sites and studies are performing.”

Resources for Site Networks

CCeSource
Blog Post
The COVID-19 pandemic has caused an enormous disruption in healthcare priorities and staffing, and as restrictions on people’s movement have increased, clinical research sites face unprecedented challenges to adjust studies and patient engagement accordingly. The FDA has provided guidance to support ongoing continuity and response efforts, wherein the safety of trial participants is paramount. It […]

Revolutionize the way you conduct clinical research.

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